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MEPS Home Medical Expenditure Panel Survey
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MEPS HC-135A: 2010 Prescribed Medicines
August 2012
Agency for Healthcare Research and Quality
Center for Financing, Access, and Cost Trends
540 Gaither Road
Rockville, MD 20850
(301) 427-1406

Table of Contents

A. Data Use Agreement
B. Background
1.0 Household Component (HC)
2.0 Medical Provider Component (MPC)
3.0 Survey Management and Data Collection
C. Technical Information
1.0 General Information
2.0 Data File Information
2.1 Codebook Structure
2.2 Reserved Codes
2.3 Codebook Format
2.4 Variable Naming Conventions
2.4.1 General
2.4.2 Expenditure and Source of Payment Variables
2.5 Data Collection
2.5.1 Methodology for Collecting Household-Reported Variables
2.5.2 Methodology for Collecting Pharmacy-Reported Variables
2.6 File Contents
2.6.1 Survey Administration Variables
2.6.1.1 Person Identifier Variables (DUID, PID, DUPERSID)
2.6.1.2 Record Identifier Variables (RXRECIDX, LINKIDX, DRUGIDX)
2.6.1.3 Panel Variable (PANEL)
2.6.1.4 Round Variable (PURCHRD)
2.6.2 Characteristics of Prescribed Medicine Events
2.6.2.1 Date When Prescribed Medicine Was First Taken (RXBEGDD-RXBEGYRX)
2.6.2.2 Prescribed Medicine Attributes (RXNAME-RXDAYSUP)
2.6.2.3 Type of Pharmacy (PHARTP1-PHARTP7)
2.6.2.4 Analytic Flag Variables (RXFLG-INPCFLG)
2.6.2.5 Free Sample Variable (SAMPLE)
2.6.2.6 Condition Codes (RXICD1X-RXICD3X) and Clinical Classification Codes (RXCCC1X-RXCCC3X)
2.6.3 Multum Lexicon Variables from Cerner Multum, Inc.
2.6.4 Expenditure Variables (RXSF10X-RXXP10X)
2.6.4.1 Definition of Expenditures
2.6.4.2 Sources of Payment
3.0 Sample Weight (PERWT10F)
3.1 Overview
3.2 Details on Person Weight Construction
3.2.1 MEPS Panel 14 Weight
3.2.2 MEPS Panel 15 Weight
3.2.3 The Final Weight for 2010
3.3 Coverage
3.4 Using MEPS Data for Trend Analysis
4.0 General Data Editing and Imputation Methodology
4.1 Rounding
4.2 Edited/Imputed Expenditure Variables (RXSF10X-RXXP10X)
5.0 Strategies for Estimation
5.1 Developing Event-Level Estimates
5.2 Person-Based Estimates for Prescribed Medicine Purchases
5.3 Variables with Missing Values
5.4 Variance Estimation (VARSTR, VARPSU)
6.0 Merging/Linking MEPS Data Files
6.1 Linking to the Person-Level File
6.2 Linking to the Medical Conditions File
6.3 Longitudinal Analysis
_._ References
D. Variable-Source Crosswalk
Appendix 1: Definitions for RXFORM, Form of Prescribed Medicines
Appendix 2: Definitions for RXFRMUNT, Unit of Measure for Form of Prescribed Medicines
Appendix 3: Definitions for RXSTRUNT, Unit of Measure for Strength of Prescribed Medicines
Appendix 4: Definitions of Therapeutic Class Code

A. Data Use Agreement

Individual identifiers have been removed from the micro-data contained in these files. Nevertheless, under sections 308 (d) and 903 (c) of the Public Health Service Act (42 U.S.C. 242m and 42 U.S.C. 299 a-1), data collected by the Agency for Healthcare Research and Quality (AHRQ) and/or the National Center for Health Statistics (NCHS) may not be used for any purpose other than for the purpose for which they were supplied; any effort to determine the identity of any reported cases is prohibited by law.

Therefore in accordance with the above referenced Federal Statute, it is understood that:

  1. No one is to use the data in this data set in any way except for statistical reporting and analysis; and
     
  2. If the identity of any person or establishment should be discovered inadvertently, then (a) no use will be made of this knowledge, (b) the Director Office of Management AHRQ will be advised of this incident, (c) the information that would identify any individual or establishment will be safeguarded or destroyed, as requested by AHRQ, and (d) no one else will be informed of the discovered identity; and
     
  3. No one will attempt to link this data set with individually identifiable records from any data sets other than the Medical Expenditure Panel Survey or the National Health Interview Survey.

By using these data you signify your agreement to comply with the above stated statutorily based requirements with the knowledge that deliberately making a false statement in any matter within the jurisdiction of any department or agency of the Federal Government violates Title 18 part 1 Chapter 47 Section 1001 and is punishable by a fine of up to $10,000 or up to 5 years in prison.

The Agency for Healthcare Research and Quality requests that users cite AHRQ and the Medical Expenditure Panel Survey as the data source in any publications or research based upon these data.

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B. Background

1.0 Household Component (HC)

The Medical Expenditure Panel Survey (MEPS) provides nationally representative estimates of health care use, expenditures, sources of payment, and health insurance coverage for the U.S. civilian non-institutionalized population. The MEPS Household Component (HC) also provides estimates of respondents' health status, demographic and socio-economic characteristics, employment, access to care, and satisfaction with health care. Estimates can be produced for individuals, families, and selected population subgroups. The panel design of the survey, which includes 5 Rounds of interviews covering 2 full calendar years, provides data for examining person level changes in selected variables such as expenditures, health insurance coverage, and health status. Using computer assisted personal interviewing (CAPI) technology, information about each household member is collected, and the survey builds on this information from interview to interview. All data for a sampled household are reported by a single household respondent.

The MEPS-HC was initiated in 1996. Each year a new panel of households is selected. Because the data collected are comparable to those from earlier medical expenditure surveys conducted in 1977 and 1987, it is possible to analyze long-term trends. Each annual MEPS-HC sample size is about 15,000 households. Data can be analyzed at either the person or event level. Data must be weighted to produce national estimates.

The set of households selected for each panel of the MEPS HC is a subsample of households participating in the previous year's National Health Interview Survey (NHIS) conducted by the National Center for Health Statistics. The NHIS sampling frame provides a nationally representative sample of the U.S. civilian non-institutionalized population and reflects an oversample of blacks and Hispanics. In 2006, the NHIS implemented a new sample design, which included Asian persons in addition to households with black and Hispanic persons in the oversampling of minority populations. MEPS oversamples additional policy relevant sub-groups such as Asians and low income households. The linkage of the MEPS to the previous year's NHIS provides additional data for longitudinal analytic purposes.

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2.0 Medical Provider Component (MPC)

Upon completion of the household CAPI interview and obtaining permission from the household survey respondents, a sample of medical providers are contacted by telephone to obtain information that household respondents can not accurately provide. This part of the MEPS is called the Medical Provider Component (MPC) and information is collected on dates of visit, diagnosis and procedure codes, charges and payments. The Pharmacy Component (PC), a subcomponent of the MPC, does not collect charges or diagnosis and procedure codes but does collect drug detail information, including National Drug Code (NDC) and medicine name, as well as date filled and sources and amounts of payment. The MPC is not designed to yield national estimates. It is primarily used as an imputation source to supplement/replace household reported expenditure information.

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3.0 Survey Management and Data Collection

MEPS HC and MPC data are collected under the authority of the Public Health Service Act. Data are collected under contract with Westat, Inc. (MEPS HC) and Research Triangle Institute (MEPS MPC). Data sets and summary statistics are edited and published in accordance with the confidentiality provisions of the Public Health Service Act and the Privacy Act. The National Center for Health statistics (NCHS) provides consultation and technical assistance.

As soon as data collection and editing are completed, the MEPS survey data are released to the public in staged releases of summary reports, micro data files, and tables via the MEPS web site: meps.ahrq.gov . Selected data can be analyzed through MEPSnet, an on-line interactive tool designed to give data users the capability to statistically analyze MEPS data in a menu-driven environment.

Additional information on MEPS is available from the MEPS project manager or the MEPS public use data manager at the Center for Financing Access and Cost Trends, Agency for Healthcare Research and Quality, 540 Gaither Road, Rockville, MD 20850 (301-427-1406).

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C. Technical Information

1.0 General Information

This documentation describes one in a series of public use event files from the 2010 Medical Expenditure Panel Survey (MEPS) Household Component (HC) and Medical Provider Component (MPC). Released as an ASCII data file (with related SAS, SPSS, and Stata programming statements) and SAS transport file, the 2010 Prescribed Medicines public use file provides detailed information on household reported prescribed medicines for a nationally representative sample of the civilian noninstitutionalized population of the United States. Data from the Prescribed Medicines event file can be used to make estimates of prescribed medicine utilization and expenditures for calendar year 2010. The file contains 70 variables and has a logical record length of 536 with an additional 2-byte carriage return/line feed at the end of each record. As illustrated below, this file consists of MEPS survey data obtained in the 2010 portion of Round 3 and Rounds 4 and 5 for Panel 14, as well as Rounds 1, 2 and the 2010 portion of Round 3 for Panel 15 (i.e., the rounds for the MEPS panels covering calendar year 2010).

This image illustrates that in 2010 information was collected in the 2010 portion of Round 3 and the complete Rounds 4 and 5 of Panel 14, and in the complete Rounds 1 and 2 and the 2010 portion of Round 3 of Panel 15.

Each record on this event file represents a unique prescribed medicine event; that is, a prescribed medicine reported as being purchased by the household respondent. In addition to expenditures related to the prescribed medicine, each record contains household reported characteristics and medical conditions associated with the prescribed medicine.

Data from this event file can be merged with other 2010 MEPS-HC data files, for purposes of appending person characteristics such as demographic or health insurance coverage to each prescribed medicine record.

Counts of prescribed medicine utilization are based entirely on household reports. Information from the Pharmacy Component (PC) (within the MEPS-MPC, see Section B 2.0 for more details on the MPC) was used to provide expenditure and payment data, as well as details of the medication (e.g., strength, quantity, etc.).

The file can be used to construct summary variables of expenditures, sources of payment, and other aspects of utilization of prescribed medicines. Aggregate annual person-level information on the use of prescribed medicines and other health services use is provided on the 2010 Full Year Consolidated Data File, where each record represents a MEPS sampled person.

The following documentation offers a brief overview of the types and levels of data provided and the content and structure of the files and the codebook. It contains the following sections:

Data File Information
Sample Weight
General Data Editing and Imputation Methodology
Strategies for Estimation
Merging/Linking MEPS Data Files
References
Variable to Source Crosswalk

For more information on MEPS HC survey design see T. Ezzati-Rice, et al. (1998-2007) and S. Cohen, 1996. For information on the MEPS MPC design, see S. Cohen, 1998. A copy of the survey instrument used to collect the information on this file is available on the MEPS Web site at the following address: meps.ahrq.gov.

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2.0 Data File Information

The 2010 Prescribed Medicines public use data set contains 301,032 prescribed medicine records. Each record represents one household reported prescribed medicine that was purchased during calendar year 2010. Of the 301,032 prescribed medicine records, 295,028 records are associated with persons having a positive person-level weight (PERWT10F). The persons represented on this file had to meet either criterion a or b below:

  1. Be classified as a key in-scope person who responded for his or her entire period of 2010 eligibility (i.e., persons with a positive 2010 full-year person-level sampling weight (PERWT10F > 0), or
     
  2. Be an eligible member of a family all of whose key in-scope members have a positive person-level weight (PERWT10F > 0). (Such a family consists of all persons with the same value for FAMIDYR.) That is, the person must have a positive full-year family-level weight (FAMWT10F >0). Note that FAMIDYR and FAMWT10F are variables on the 2010 Population Characteristics file.

Persons with no prescribed medicine use for 2010 are not included on this file (but are represented on MEPS person-level files). A codebook for the data file is provided (in file H135acb.pdf).

This file includes prescribed medicine records for all household members who resided in eligible responding households and for whom at least one prescribed medicine was reported. Only prescribed medicines that were purchased in calendar year 2010 are represented on this file. This file includes prescribed medicines identified in the Prescribed Medicines (PM) section of the HC survey instrument, as well as those prescribed medicines identified in association with other medical events. Each record on this file represents a single acquisition of a prescribed medicine reported by household respondents. Some household members may have multiple acquisitions of prescribed medicines and thus will be represented in multiple records on this file. Other household members may have no reported acquisitions of prescribed medicines and thus will have no records on this file.

When diabetic supplies, such as syringes and insulin, were mentioned in the Other Medical Expenses (OM) section of the MEPS-HC, the interviewer was directed to collect information on these items in the Prescribed Medicines section of the MEPS questionnaire. The respondent was also asked the questions in the Charge Payment (CP) section of the HC. To the extent that these items are purchased without a prescription, they represent a non-prescription addition to the MEPS prescription drug expenditure and utilization data. Although these items may be purchased without a prescription, a prescription purchase may be required to obtain third party payments. Analysts are free to code and define diabetic supply/equipment and insulin events utilizing their own coding mechanism. If desired, this would enable analysts to subset the Prescribed Medicines file to exclude these types of events.

It should also be noted that refills are included on this file. The HC obtains information on the name of the prescribed medicine and the number of times the medicine was obtained. The data collection design for the HC does not allow separate records to be created for multiple acquisitions of the same prescribed medicine. However, in the PC, each original purchase, as well as any refill, is considered a unique prescribed medicine event. Therefore, for the purposes of editing, imputation, and analysis, all records in the HC were "unfolded" to create separate records for each original purchase and each refill. Please note that for multiple acquisitions of the same drug, MEPS did not collect information in the HC to distinguish between the original purchase and refills. The survey only collected data on the number of times a prescribed medicine was acquired during a round. In some cases, all purchases may have been refills of an original purchase in a prior round or prior to the survey year. The file also includes a variable, SAMPLE, which indicates whether or not the household reported receiving a free sample of that drug in that round. (To obtain more details on free samples, please see Section 2.6.2.5.)

Each record on this file includes the following: an identifier for each unique prescribed medicine; detailed characteristics associated with the event (e.g., national drug code (NDC), medicine name, selected Multum Lexicon variables [see Section 2.6.3 for more information on the Multum Lexicon variables included on this file], etc.); conditions, if any, associated with the medicine; the date on which the person first used the medicine; total expenditure and sources of payments; types of pharmacies that filled the household’s prescriptions; whether the prescription is one of which the household received a free sample during the round; and a full-year person-level weight.

Data from this file can be merged with previously released MEPS-HC person-level data using the unique person identifier, DUPERSID, to append person characteristics such as demographic or health insurance coverage to each record. Data from this file can also be merged with the 2010 Full Year Consolidated Data File to estimate expenditures for persons with prescribed medicines. The Prescribed Medicines event file can also be linked to the MEPS 2010 Medical Conditions File and additional MEPS 2010 event files. Please see the 2010 Appendix File for details on how to link MEPS data files.

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2.1 Codebook Structure

For each variable on the file, both weighted and unweighted frequencies are provided. The codebook and data file sequence list variables in the following order:

Unique person identifiers
Unique prescribed medicine identifiers
Other survey administration variables
Prescribed medicine characteristics variables
ICD-9 codes for medical conditions
Clinical Classification Software codes for medical conditions
Multum Lexicon variables
Expenditure variables
Weight and variance estimation variables

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2.2 Reserved Codes

The following reserved code values are used:

Value Definition
-1 INAPPLICABLE Question was not asked due to skip pattern
-7 REFUSED Question was asked and respondent refused to answer question
-8 DK Question was asked and respondent did not know answer
-9 NOT ASCERTAINED Interviewer did not record the data
-14 NOT YET TAKEN/USED Respondent answered that the medicine has not yet been used

Generally, values of -1, -7, -8 and -9 have not been edited on this file. However, this is not true if the pharmacist determined a prescription drug name to be a confidentiality risk. In these instances, the corresponding NDC was replaced with -9, and the Multum Lexicon therapeutic class replaced the drug name determined to be a confidentiality risk. The values of -1 and -9 can be edited by analysts by following the skip patterns in the questionnaire. The value -14 was a valid value only for the variable representing the year the household member first used the medicine (RXBEGYRX). RXBEGYRX = -14 means that when the interviewer asked the respondent the year the household member first started using the medicine, he/she responded that the household member had not yet started using the medicine (See section C, 2.6.2.1).

A copy of the Household Component questionnaire can be found at meps.ahrq.gov/survey_comp/survey_questionnaires.jsp by selecting Prescribed Medicines (PM) from the questionnaire section.

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2.3 Codebook Format

The codebook describes an ASCII data set (although the data are also being provided in a SAS transport file). The following codebook items are provided for each variable:

Identifier Description
Name Variable name (maximum of 8 characters)
Description Variable descriptor (maximum 40 characters)
Format Number of bytes
Type Type of data: numeric (indicated by NUM) or character (indicated by CHAR)
Start Beginning column position of variable in record
End Ending column position of variable in record

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2.4 Variable Naming Conventions

In general, variable names reflect the content of the variable, with an eight-character limitation. Generally, all imputed/edited variables end with an "X."

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2.4.1 General

Variables contained on this file were derived from the HC questionnaire itself, the MPC data collection instrument, the CAPI, or from the Multum Lexicon database from Cerner Multum, Inc. The source of each variable is identified in Section D, entitled "Variable-Source Crosswalk." Sources for each variable are indicated in one of five ways:

  1. Variables which are derived from CAPI or assigned in sampling are so indicated as "CAPI derived" or "Assigned in sampling," respectively;
     
  2. Variables which come from one or more specific questions have those numbers and the questionnaire section indicated in the "Source" column;
     
  3. Variables constructed from multiple questions using complex algorithms are labeled "Constructed" in the "Source" column;
     
  4. Variables which have been imputed are so indicated; and
     
  5. Variables derived from the Multum Lexicon database are so indicated.

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2.4.2 Expenditure and Source of Payment Variables

Only imputed/edited versions of the expenditure variables are provided on the file. Expenditure variables on this event file follow a standard naming convention and are 7 characters in length.

The 12 source of payment variables and one sum of payments variable are named consistently in the following way:

The first two characters indicate the type of event:

IP - inpatient stay
ER - emergency room visit
HH - home health event
OM - other medical equipment
OB - office-based visit
OP - outpatient visit
DV - dental visit
RX - prescribed medicine

In the case of the source of payment variables, the third and fourth characters indicate:

SF - self or family
MR - Medicare
MD - Medicaid
PV - private insurance
VA - Veterans Administration/CHAMPVA
TR - TRICARE
OF - other Federal Government
SL - State/local government
WC - Workers’ Compensation
OT - other insurance
OR - other private
OU - other public
XP - sum of payments

The fifth and sixth characters indicate the year (10). The seventh character, "X", indicates the variable is edited/imputed.

For example, RXSF10X is the edited/imputed amount paid by self or family for the 2010 prescribed medicine expenditure.

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2.5 Data Collection

Data regarding prescription drugs were obtained through the HC questionnaire and a pharmacy follow-back component (within the Medical Provider Component).

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2.5.1 Methodology for Collecting Household-Reported Variables

During each round of the MEPS-HC, respondents were asked to supply the name of any prescribed medicine they or their family members purchased or otherwise obtained during that round. For each medicine in each round, the following information was collected: whether any free samples of the medicine were received; the name(s) of any health problems the medicine was prescribed for; the number of times the prescription medicine was obtained or purchased; the year, month, and day on which the person first used the medicine; and a list of the names, addresses, and types of pharmacies that filled the household’s prescriptions. In the HC, respondents were asked if they send in claim forms for their prescriptions or if their pharmacy providers do this automatically for them at the point of purchase. For those who said their pharmacy providers automatically send in claims for them at the point of purchase, charge and payment information was collected in the pharmacy follow-back component (unless the purchase was an insulin or diabetic supply/equipment event that was mentioned in the household component; see Section 4.0 for details). However, charge and payment information was collected for those who said they send in their own prescription claim forms, because it is thought that payments by private third-party payers for those who filed their own claim forms for prescription purchases would not be available from pharmacies. Uninsured persons were treated in the same manner as those whose pharmacies filed their prescription claims at the point of purchase. Persons who said they did not know if they sent in their own prescription claim forms were treated as those who said they did send in their own prescription claim forms.

In consultation with an industry expert, outlier values for the number of times a household reported purchasing or otherwise obtaining a prescription drug in a particular round were determined by comparing the number of days a person was in the round and the number of times the person was reported to have obtained the drug in the round. For these events, a new value for the number of times a drug was purchased or otherwise obtained by a person in a round was imputed. In addition, for rounds in which a household respondent did not know/remember the number of times a certain prescribed medicine was purchased or otherwise obtained, the number of fills or refills was imputed.

For those rounds that spanned two years, drugs mentioned in that round were allocated between the years based on the number of times the respondent said the drug was purchased in the respective year, the year the person started taking the drug, the length of the person’s round, the dates of the person’s round, and the number of drugs for that person in the round. In addition, a "folded" version of the PC on a drug level, as opposed to an acquisition level, was used for these types of events to assist in determining how many acquisitions of the drug should be allocated between the years.

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2.5.2 Methodology for Collecting Pharmacy-Reported Variables

If the household member with the prescription gave written permission to release his or her pharmacy records, pharmacy providers identified by the household were contacted by telephone for the pharmacy follow-back component. Following an initial telephone contact, the signed permission forms and materials explaining the study were faxed (or mailed) to cooperating pharmacy providers. The materials informed the providers of all persons participating in the survey who had prescriptions filled at their place of business and requested a computerized printout of all prescriptions filled for each person. Starting with the 2009 pharmacy data collection, pharmacies could choose to report information in computer assisted telephone interviews (CATI). The CATI instrument was also used to enter information from printouts. For each medication listed, the following information was requested: date filled; national drug code (NDC); medication name; strength of medicine (amount and unit); quantity (package size/amount dispensed); and payments by source. Starting with the 2009 pharmacy data collection, when an NDC was provided, often the drug name and other drug characteristics were obtained from secondary proprietary data sources.

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2.6 File Contents

2.6.1 Survey Administration Variables

2.6.1.1 Person Identifier Variables (DUID, PID, DUPERSID)

The dwelling unit ID (DUID) is a five-digit random number assigned after the case was sampled for MEPS. The three-digit person number (PID) uniquely identifies each person within the dwelling unit. The eight-character variable DUPERSID uniquely identifies each person represented on the file and is the combination of the variables DUID and PID. For detailed information on dwelling units and families, please refer to the documentation for the 2010 Full Year Population Characteristics File.

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2.6.1.2 Record Identifier Variables (RXRECIDX, LINKIDX, DRUGIDX)

The variable RXRECIDX uniquely identifies each record on the file. This 15-character variable comprises the following components: prescribed medicine drug-round-level identifier generated through the HC (positions 1-12) + enumeration number (positions 13-15). The prescribed medicine drug-round-level ID generated through the HC (positions 1-12) can be used to link a prescribed medicine event to the conditions file and to other event files, via link files, and is provided on this file as the variable LINKIDX. For more details on linking, please refer to Section 6.2 and to the 2010 Appendix File. The prescribed medicine drug-level ID generated through the HC, DRUGIDX, can be used to link drugs across rounds. DRUGIDX was first added to the file for 2009; for 1996 through 2008, the RXNDC linked drugs across rounds.

The following hypothetical example illustrates the structure of these ID variables. This example illustrates a person in Rounds 1 and 2 of the household interview who reported having purchased Amoxicillin three times. The following example shows three acquisition-level records, all having the same DRUGIDX (00002026002), for one person (DUPERSID=00002026) in two rounds. Generally, within a round, one NDC is associated with a prescribed medicine event because matching was performed at a drug level, as opposed to an acquisition level. The LINKIDX (000020260083) remains the same for both records in Round 1 but varies across rounds. The RXRECIDX (000020260083001, 000020260083002, 000020260103001) differs for all three records.

DUPERSID PURCHRD RXRECIDX LINKIDX DRUGIDX RXNDC
00002026 1 000020260083001 000020260083 00002026002 00093310905
00002026 1 000020260083002 000020260083 00002026002 00093310905
00002026 2 000020260103001 000020260103 00002026002 00003010955

Starting with the 2008 Prescribed Medicines file, there can be multiple RXNDCs for a LINKIDX. All the acquisitions in the LINKIDX represent the same drug (active ingredients), but the RXNDCs may represent different manufacturers. (For more details on matching, please see Section 4.0).

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2.6.1.3 Panel Variable (PANEL)

PANEL is a constructed variable used to specify the panel number for the person. Panel will indicate either Panel 14 or Panel 15 for each person on the file. Panel 14 is the panel that started in 2009, and Panel 15 is the panel that started in 2010.

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2.6.1.4 Round Variable (PURCHRD)

The variable PURCHRD indicates the round in which the prescribed medicine was purchased and takes on the value of 1, 2, 3, 4, or 5. Rounds 3, 4, and 5 are associated with MEPS survey data collection from Panel 14. Similarly, Rounds 1, 2, and 3 are associated with data collected from Panel 15.

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2.6.2 Characteristics of Prescribed Medicine Events

2.6.2.1 Date When Prescribed Medicine Was First Taken (RXBEGDD-RXBEGYRX)

There are three variables which indicate when a prescribed medicine was first taken (used), as reported by the household respondent. They are the following: RXBEGDD indicates the day on which a person first started taking a medication, RXBEGMM denotes the month in which a person first started taking a medication, and RXBEGYRX reflects the year in which a person first started taking a medicine. These "first taken" questions are only asked the first time a prescription is mentioned by the household respondent. These questions are not asked about refills of the prescription in subsequent rounds. Starting with the 2009 file, values were carried forward from prior rounds for all medications first reported in 2009. Users should also note that the value -14 (not yet used or taken) is not relevant for refills. The variable DRUGIDX (see Section 2.6.1.2) can be used to determine whether a medication was reported in a prior round. For purposes of confidentiality, RXBEGYRX was bottom-coded at 1925, consistent with top-coding of the age variables on the 2010 Full Year Population Characteristics Public Use File (HC-132).

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2.6.2.2 Prescribed Medicine Attributes (RXNAME-RXDAYSUP)

For each prescribed medicine included on this file, several data items collected describe in detail the medication obtained or purchased. These data items are the following:

  1. Medication name - pharmacy reported (RXNAME)
     
  2. National drug code (RXNDC)
     
  3. Quantity of the prescribed medicine dispensed (RXQUANTY), e.g., number of tablets in the prescription
     
  4. Form of the prescribed medicine (RXFORM), e.g., powder
     
  5. Unit of measurement for form of Rx/prescribed medicine (RXFRMUNT), e.g., oz
     
  6. Strength of the dose of the prescribed medicine (RXSTRENG), e.g., 10
     
  7. Unit of measurement for the strength of the dose of the prescribed medicine (RXSTRUNT), e.g., gm
     
  8. Days supplied (RXDAYSUP)

Days supplied was first collected and released to the public on the 2010 Prescribed Medicines file. Many pharmacies did not provide this information, and imputation was not attempted in these cases. A value of 999 indicates the medication is to be taken as needed. No edits were implemented to impose consistency between the quantity and days supplied, and no edits were implemented for very high values.

The 2010 file contains multiple values of RXFORM and RXFRMUNT not found in Prescribed Medicines files in prior years. There was no reconciliation of inconsistencies or duplication between RXFORM and RXFRMUNT. Please refer to Appendices 1, 2, and 3 for definitions for RXFORM, RXFRMUNT, and RXSTRUNT abbreviations, codes and symbols. Please refer to Appendix 4 for therapeutic class code definitions.

The national drug code (NDC) is an 11-digit code. The first 5 digits indicate the manufacturer of the prescribed medicine. The next 4 digits indicate the form and strength of the prescription, and the last 2 digits indicate the package size from which the prescription was dispensed. NDC values were imputed from a proprietary database to certain PC prescriptions because the NDC reported by the pharmacy provider was not valid. These records are identified by RXFLG=3.

For the years 1996-2004, AHRQ’s licensing agreement for the proprietary database precluded the release of the imputed NDC values to the public, so for these prescriptions, the household-reported name of the prescription (RXHHNAME) and the original NDC (RXNDC) and prescription name (RXNAME) reported by the pharmacy were provided on the file to allow users to do their own imputation. In addition, for the years 1996-2004, the imputed NDC values for the RXFLG=3 cases could be accessed through the MEPS Data Center. For those events not falling into the RXFLG=3 category, the reserve code (-13) was assigned to the household-reported medication name (RXHHNAME). The household-reported name of the prescription (RXHHNAME) is no longer provided on this file; however, this variable may be accessed through the MEPS Data Center as can the original pharmacy-reported name and NDC. For information on accessing data through the MEPS Data Center, see the Data Center section of the MEPS Web site at: meps.ahrq.gov/data_stats/onsite_datacenter.jsp.

Imputed data on this event file, unlike other MEPS event files, may still have missing data. This is because imputed data on this file are imputed from the PC or from a proprietary database. These sources did not always include complete information for each variable but did include an NDC, which would typically enable an analyst to obtain any missing data items. For example, although there are a substantial number of missing values for the strength of the prescription that were not supplied by the pharmacist, these missing values were not imputed because this information is embedded in the NDC.

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2.6.2.3 Type of Pharmacy (PHARTP1-PHARTP7)

Household respondents were asked to list the type of pharmacy from which household members purchased their medications. A respondent could list multiple pharmacies associated with each member’s prescriptions in a given round or over the course of all rounds combined covering the survey year. All household-reported pharmacies are provided on this file, but there is no link in the survey or in the data file enabling users to know the type of pharmacy from which a specific prescription was obtained if multiple pharmacies are listed. The variables PHARTP1 through PHARTP7 identify the types of pharmacy providers from which the person’s prescribed medicines were purchased. The possible types of pharmacies include the following: (1) mail-order, (2) another store, (3) HMO/clinic/hospital, (4) drug store, and (5) on-line. A -1 value for PHARTPn indicates that the household did not report "nth" pharmacy.

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2.6.2.4 Analytic Flag Variables (RXFLG-INPCFLG)

There are four flag variables included on this file (RXFLG, PCIMPFLG, CLMOMFLG, and INPCFLG).

RXFLG indicates whether or not there was any imputation performed on this record for the NDC variable, and if imputed, from what source the NDC was imputed. If no imputation was performed, RXFLG = 1. If the imputation source was another PC record, RXFLG = 2. Similarly, if the imputation source was a secondary, proprietary database and not the PC database, RXFLG = 3.

PCIMPFLG indicates the type of match between a household-reported event and a PC-reported event. PCIMPFLG = 1 indicates an exact match for a specific event for a person between the PC and the HC. PCIMPFLG = 2 indicates not an exact match between the PC and HC for a specific person (i.e., a person’s household-reported event did not have a matched counterpart in the person’s corresponding PC records). PCIMPFLG assists analysts in determining which records have the strongest link to data reported by a pharmacy. It should be noted that whenever there are multiple purchases of a unique prescribed medication in a given round, MEPS did not collect information that would enable designating any single purchase as the "original" purchase at the time the prescription was first filled, and then designating other purchases as "refills." The user needs to keep this in mind when the purchases of a medication are referred to as "refills" in the documentation. Because matching was performed at a drug level as opposed to an acquisition level, the values for PCIMPFLG are either 1 or 2. For more details on general data editing/imputation methodology, please see Section 4.0.

CLMOMFLG indicates if a prescription medicine event went through the Charge Payment (CP) section of the HC. Prescription medicine events that went through the CP section of the HC include: (1) events where the person filed their own prescription claim forms with their insurance company, (2) events for persons for whom the respondent did not know if they filed their own prescription claim forms with their insurance company, and (3) insulin and diabetic supply/equipment events (OMTYPE = 2 or 3) that were mentioned in the Other Medical Expenses section of the HC. For these types of events, information on payment sources was retained to the extent that these data were reported by the household respondent in the CP section of the HC.

INPCFLG denotes whether or not a household member had at least one prescription drug purchase in the PC (0 = no, 1 = yes).

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2.6.2.5 Free Sample Variable (SAMPLE)

SAMPLE indicates if a respondent reported the person received a free sample of the prescription medicine in the round (0 = no, 1 = yes). Respondents were asked in each round whether or not the person received any free samples of a reported prescribed medicine during the round. However, respondents were not asked to report the number of free samples a person received, nor was it made clear that free samples were included in the count of the number of times that the respondent reported a person purchasing or otherwise obtaining the prescribed medicine during the round. It is important for analysts to note that SAMPLE is not a count variable of free samples; SAMPLE = 1 indicates that a person was reported getting a free sample of the prescribed medicine during the round. This flag variable simply allows individual analysts to determine for themselves how free samples should be handled in their analysis.

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2.6.2.6 Condition Codes (RXICD1X-RXICD3X) and Clinical Classification Codes (RXCCC1X-RXCCC3X)

Information on household-reported medical conditions associated with each prescribed medicine event is provided on this file. There are up to three condition and clinical classification codes listed for each prescribed medicine event (99.75 percent of prescribed medicine events have 0-3 condition records linked). To obtain complete information associated with an event, the analyst must link to the 2010 Medical Conditions File. Details on how to link to the MEPS 2010 Medical Conditions File are provided in the 2010 Appendix File. The user should note that, for confidentiality restrictions, provider-reported condition information (for non-prescription medicines events) is not publicly available. Provider-reported condition data for non-prescription medicines events can be accessed only through the MEPS Data Center.

The medical conditions reported by the HC respondent were recorded by the interviewer as verbatim text, which were then coded to fully-specified 2010 ICD-9-CM codes, including medical condition, V-codes, and a small number of E-codes, by professional coders. Although codes were verified and error rates did not exceed 2.5 percent for any coder, analysts should not presume this level of precision in the data; the ability of household respondents to report condition data that can be coded accurately should not be assumed. For detailed information on conditions, please refer to the documentation on the 2010 Medical Conditions File. For frequencies of conditions by event type, please see the 2010 Appendix File, HC-135I.

The ICD-9-CM condition codes were aggregated into clinically meaningful categories. These categories, included on the file as RXCCC1X-RXCCC3X, were generated using Clinical Classification Software (CCS) (formerly known as Clinical Classifications for Health Care Policy Research (CCHPR)), which aggregates conditions and V-codes into mutually exclusive categories, most of which are clinically homogeneous.

In order to preserve household member confidentiality, nearly all of the condition codes provided on this file have been collapsed from fully-specified codes to 3-digit code categories. The reported ICD-9-CM code values were mapped to the appropriate clinical classification category prior to being collapsed to the 3-digit categories. Because of this collapsing, it is possible for there to be duplicate 3-digit ICD-9-CM condition codes linked to a single prescribed medicine event when different fully-specified codes are collapsed into the same code. This would result in two or more of the condition code variables on this file being set to the same value on a single record. For more information on ICD-9-CM codes, see the HC-137 documentation.

The condition codes (and clinical classification codes) linked to each prescribed medicine event are sequenced in the order in which the conditions were reported by the household respondent, which was in chronological order of reporting and not in order of importance or severity. Analysts who use the 2010 Medical Conditions file in conjunction with this prescribed medicines event file should note that the conditions on this file are sorted differently than they appear on the Medical Conditions file.

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2.6.3 Multum Lexicon Variables from Cerner Multum, Inc.

Each record on this file contains the following Multum Lexicon variables:

PREGCAT: pregnancy category variable - identifies the FDA pregnancy category to which a particular drug has been assigned

TCn: therapeutic classification variable - assigns a drug to one or more therapeutic/chemical categories; can have up to three categories per drug

TCnSn: therapeutic sub-classification variable - assigns one or more sub-categories to a more general therapeutic class category given to a drug

TCnSn_n: therapeutic sub sub-classification variable - assigns one or more sub sub-categories to a more general therapeutic class category and sub-category given to a drug

Users should carefully review the data when conducting trend analyses or pooling years or panels because Multum’s therapeutic classification has changed across the years of the MEPS. The Multum variables on each year of the MEPS Prescribed Medicines files reflect the most recent classification available in the year the data were released. Since the release of the 1996 Prescribed Medicines file, the Multum classification has been changed by the addition of new classes and subclasses, and by changes in the hierarchy of classes. Three examples follow: 1) In the 1996-2004 Prescribed Medicines files, antidiabetic drugs are a subclass of the hormone class, but in subsequent files, the antidiabetic subclass is part of a class of metabolic drugs. 2) In the 1996-2004 files, antihyperlipidemic agents are categorized as a class with a number of subclasses including HMG-COA reductase inhibitors (statins). In subsequent files, antihyperlipidemic drugs are a subclass, and HMG-COA reductase inhibitors are a sub-subclass, in the metabolic class. 3) In the 1996-2004 files, the psychotherapeutic class comprises drugs from four subclasses: antidepressants, antipsychotics, anxiolytics/sedatives/hypnotics, and CNS stimulants. In subsequent files, the psychotherapeutic class comprises only antidepressants and antipsychotics. Changes may occur between any years. For additional information on these and other Multum Lexicon variables, as well as the Multum Lexicon database itself, please refer to www.multum.com/Lexicon.htm.

Researchers using the Multum Lexicon variables are requested to cite Multum Lexicon as the data source.

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2.6.4 Expenditure Variables (RXSF10X-RXXP10X)

2.6.4.1 Definition of Expenditures

Expenditures on this file refer to what is paid for health care services. More specifically, expenditures in MEPS are defined as the sum of payments for care received, including out-of-pocket payments and payments made by private insurance, Medicaid, Medicare, and other sources. The definition of expenditures used in MEPS differs slightly from its predecessors, the 1987 NMES and 1977 NMCES surveys, where "charges" rather than "sum of payments" were used to measure expenditures. This change was adopted because charges became a less appropriate proxy for medical expenditures during the 1990s because of the increasingly common practice of discounting charges. Although measuring expenditures as the sum of payments incorporates discounts in the MEPS expenditure estimates, the estimates do not incorporate any manufacturer or other rebates associated with Medicaid or other purchases. Another general change from the two prior surveys is that charges associated with uncollected liability, bad debt, and charitable care (unless provided by a public clinic or hospital) are not counted as expenditures, because there are no payments associated with those classifications. For details on expenditure definitions, please reference the following, "Informing American Health Care Policy" (Monheit, Wilson, Arnett, 1999).

If examining trends in MEPS expenditures or performing longitudinal analysis on MEPS expenditures please refer to Section C, sub-sections 3.4 and 6.3 respectively for more information.

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2.6.4.2 Sources of Payment

In addition to total expenditures, variables are provided which itemize expenditures according to major source of payment categories. These categories are:

  1. Out-of-pocket by user (self) or family,
  2. Medicare,
  3. Medicaid,
  4. Private Insurance,
  5. Veterans Administration/CHAMPVA, excluding TRICARE
  6. TRICARE,
  7. Other Federal sources – includes Indian Health Service, Military Treatment Facilities, and other care by the Federal government,
  8. Other State and Local Source – includes community and neighborhood clinics, State and local health departments, and State programs other than Medicaid,
  9. Workers’ Compensation, and
  10. Other Unclassified Sources – includes sources such as automobile, homeowner’s, and liability insurance, and other miscellaneous or unknown sources.

    Two additional source of payment variables were created to classify payments for events with apparent inconsistencies between insurance coverage and sources of payment based on data collected in the survey. These variables include:

  11. Other Private – any type of private insurance payments reported for persons not reported to have any private health insurance coverage during the year as defined in MEPS, and
  12. Other Public – Medicare/Medicaid payments reported for persons who were not reported to be enrolled in the Medicare/Medicaid program at any time during the year.

Though relatively small in magnitude, data users/analysts should exercise caution when interpreting the expenditures associated with these two additional sources of payment. While these payments stem from apparent inconsistent responses to health insurance and source of payment questions in the survey, some of these inconsistencies may have logical explanations. For example, private insurance coverage in MEPS is defined as having a major medical plan covering hospital and physician services. If a MEPS sampled person did not have such coverage but had a single service type insurance plan (e.g., dental insurance) that paid for a particular episode of care, those payments may be classified as "other private." Some of the "other public" payments may stem from confusion between Medicaid and other state and local programs or may be from persons who were not enrolled in Medicaid, but were presumed eligible by a provider who ultimately received payments from the public payer.

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3.0 Sample Weight (PERWT10F)

3.1 Overview

There is a single full year person-level weight (PERWT10F) assigned to each record for each key, in-scope person who responded to MEPS for the full period of time that he or she was in-scope during 2010. A key person was either a member of a responding NHIS household at the time of interview or joined a family associated with such a household after being out-of-scope at the time of the NHIS (the latter circumstance includes newborns as well as those returning from military service, an institution, or residence in a foreign country). A person is in-scope whenever he or she is a member of the civilian noninstitutionalized portion of the U.S. population.

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3.2 Details on Person Weight Construction

The person-level weight PERWT10F was developed in several stages. Person-level weights for Panel 14 and Panel 15 were created separately. The weighting process for each panel included an adjustment for nonresponse over time and calibration to independent population figures. The calibration was initially accomplished separately for each panel by raking the corresponding sample weights to Current Population Survey (CPS) population estimates based on five variables. The five variables used in the establishment of the initial person-level control figures were: census region (Northeast, Midwest, South, West); MSA status (MSA, non-MSA); race/ethnicity (Hispanic; black, non-Hispanic; Asian, non-Hispanic; and other); sex; and age. A 2010 composite weight was then formed by multiplying each weight from Panel 14 by the factor .51 and each weight from Panel 15 by the factor .49. The choice of factors reflected the relative sample sizes of the two panels, helping to limit the variance of estimates obtained from pooling the two samples. The composite weight was again raked to the same set of CPS-based control totals. When poverty status information derived from income variables became available, a final raking was undertaken on the previously established weight variable. Control totals were established using poverty status (five categories: below poverty, from 100 to 125 percent of poverty, from 125 to 200 percent of poverty, from 200 to 400 percent of poverty, at least 400 percent of poverty) as well as the original five variables used in the previous calibrations.

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3.2.1 MEPS Panel 14 Weight

The person-level weight for MEPS Panel 14 was developed using the 2009 full year weight for an individual as a "base" weight for survey participants present in 2009. For key, in-scope members who joined an RU some time in 2010 after being out-of-scope in 2009, the initially assigned person-level weight was the corresponding 2009 family weight. The weighting process included an adjustment for nonresponse over Rounds 4 and 5 as well as raking to population control figures for December 2010. These control figures were derived by scaling back the population totals obtained from the March 2011 CPS to correspond to a national estimate for the civilian noninstitutionalized population provided by the Census Bureau for December 2010. Variables used in the establishment of person-level control figures included: census region (Northeast, Midwest, South, West); MSA status (MSA, non-MSA); race/ethnicity (Hispanic, black but non-Hispanic, Asian but non-Hispanic, and other); sex; and age. The final weight for key, responding persons who were not in-scope on December 31, 2010 but were in-scope earlier in the year was the person weight after the nonresponse adjustment.

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3.2.2 MEPS Panel 15 Weight

The person-level weight for MEPS Panel 15 was developed using the MEPS Round 1 person-level weight as a "base" weight. For key, in-scope members who joined an RU after Round 1, the Round 1 family weight served as a "base" weight. The weighting process included an adjustment for nonresponse over Round 2 and the 2010 portion of Round 3 as well as raking to the same population control figures for December 2010 used for the MEPS Panel 14 weights. The same five variables employed for Panel 14 raking (census region, MSA status, race/ethnicity, sex, and age) were used for Panel 15 raking. Again, the final weight for key, responding persons who were not in-scope on December 31, 2010 but were in-scope earlier in the year was the person weight after the nonresponse adjustment.

Note that the MEPS Round 1 weights incorporated the following components: the original household probability of selection for the NHIS; ratio-adjustment to NHIS-based national population estimates at the household (occupied dwelling unit) level; adjustment for nonresponse at the dwelling unit level for Round 1; and poststratification to figures at the family and person level obtained from the March CPS data base of the corresponding year (i.e., 2009 for Panel 14 and 2010 for Panel 15).

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3.2.3 The Final Weight for 2010

The composite weights of two groups of persons who were out-of-scope on December 31, 2010 were poststratified. Specifically, the weights of those who were in-scope some time during the year, out-of-scope on December 31, and entered a nursing home during the year were poststratified to a corresponding control total obtained from the 1996 MEPS Nursing Home Component. Those who died while in-scope during 2010 were poststratified to corresponding estimates derived using data obtained from the Medicare Current Beneficiary Survey (MCBS) and Vital Statistics information provided by the National Center for Health Statistics (NCHS). Separate decedent control totals were developed for the "65 and older" and "under 65" civilian noninstitutionalized populations.

In developing the final person-level weight for 2010 (PERWT10F), additional raking dimensions were added that reflected the MEPS 2008-09 estimated average annual distributions of office-based visits by age (under 65, 65 and over) and the proportion of persons age 65 and over with care from home health agencies. These additional adjustments were included to better reflect benchmark trends in office-based and home health care utilization. For each marginal category of the dimensions, the table below shows the ratio of the weighted number of persons that resulted from including the additional raking dimensions to that of the corresponding estimate without the additional raking dimensions.

Ratio of Adjusted to Unadjusted Weights

Number of Visits Nonelderly (AGE10X < 65) Elderly (AGE10X ≥ 65)
OFFICE-BASED
0 0.9169 0.8737
1-5 1.0137 0.9270
6-10 1.0415 1.0581
> 10 1.1905 1.1058
HOME HEALTH AGENCY
0 -- 0.9882
> 0 -- 1.1564

Overall, the weighted population estimate for the civilian noninstitutionalized population for December 31, 2010 is 304,842,384 (PERWT10F>0 and INSC1231=1). The sum of the person-level weights across all persons assigned a positive person-level weight is 308,573,977.

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3.3 Coverage

The target population for MEPS in this file is the 2010 U.S. civilian noninstitutionalized population. However, the MEPS sampled households are a subsample of the NHIS households interviewed in 2008 (Panel 14) and 2009 (Panel 15). New households created after the NHIS interviews for the respective panels and consisting exclusively of persons who entered the target population after 2008 (Panel 14) or after 2009 (Panel 15) are not covered by MEPS. Neither are previously out-of-scope persons who join an existing household but are unrelated to the current household residents. Persons not covered by a given MEPS panel thus include some members of the following groups: immigrants; persons leaving the military; U.S. citizens returning from residence in another country; and persons leaving institutions. The set of uncovered persons constitutes only a small segment of the MEPS target population.

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3.4 Using MEPS Data for Trend Analysis

MEPS began in 1996, and the utility of the survey for analyzing health care trends expands with each additional year of data. However, it is important to consider a variety of factors when examining trends over time using MEPS. Statistical significance tests should be conducted to assess the likelihood that observed trends may be attributable to sampling variation. The length of time being analyzed should also be considered. In particular, large shifts in survey estimates over short periods of time (e.g. from one year to the next) that are statistically significant should be interpreted with caution, unless they are attributable to known factors such as changes in public policy, economic conditions, or MEPS survey methodology.

Specifically, beginning with the 2007 data, the rules used to identify outlier prices for prescription medications became much less stringent than in prior years. Starting with the 2007 Prescribed Medicines file, there is less editing of prices and quantities reported by pharmacies, more variation in prices for generics, lower mean prices for generics, higher mean prices for brand name drugs, greater differences in prices between generic and brand name drugs, and a somewhat lower proportion of spending on drugs is by families, as opposed to third-party payers. Starting with the 2008 Prescribed Medicines file, improvements in the data editing changed the distribution of payments by source: (1) more spending on Medicare beneficiaries is by private insurance, rather than Medicare, and (2) less out-of-pocket payments and more Medicaid payments among Medicaid enrollees. Starting with the 2009 data, additional improvements increased public program amounts and reduced out-of-pocket payments and, for Medicare beneficiaries with both Part D and Medicaid, decreased Medicare payments and increased Medicaid and other state and local government payments. Therefore, users should be cautious in the types of comparisons they make about prescription drug spending before and after 2007, 2008, and 2009. In addition, some therapeutic class codes have changed over time.

Looking at changes over longer periods of time can provide a more complete picture of underlying trends. Analysts of MEPS data may wish to consider techniques to evaluate, smooth, or stabilize estimates of trends. Such techniques include comparing pooled time periods (e.g. 1996-97 versus 2004-05), working with moving averages, or using modeling techniques with several consecutive years of MEPS data to test the fit of specified patterns over time. Finally, researchers should be aware of the impact of multiple comparisons on Type I error (i.e., the chance of declaring an observed difference to be statistically significant when there is no difference in the population parameters). Performing numerous statistical significance tests increases the likelihood of a Type I error.

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4.0 General Data Editing and Imputation Methodology

The general approach to preparing the household prescription data for this file was to utilize the PC prescription data to impute information collected from pharmacy providers to the household drug mentions. For events that went through the Charge Payment (CP) section of the HC (events where the person filed their own prescription claim forms with their insurance company, events for persons for whom the respondent did not know if they filed their own prescription claim forms with their insurance company, and insulin and diabetic supply/equipment events (OMTYPE=2 or 3) that were mentioned in the Other Medical Expenses section of the HC), information on payment sources was retained to the extent that these data were reported by the household respondent in the CP section of the HC. A matching program was adopted to link PC drugs and the corresponding drug information to household drug mentions. To improve the quality of these matches, all drugs on the household and pharmacy files were coded using a proprietary database on the basis of the medication names provided by the household respondent and pharmacy, and, when available, the NDC provided in the pharmacy follow-back component. The matching process was done at a drug (active ingredient) level, as opposed to an acquisition level. Considerable editing was done prior to the matching to correct data inconsistencies in both data sets and to fill in missing data and correct outliers on the pharmacy file.

Drug price-per-unit outliers were analyzed on the pharmacy file by first identifying the average wholesale unit price (AWUP) of the drug by linkage through the NDC to a secondary data file. In general, prescription drug unit prices were deemed to be outliers by comparing unit prices reported in the pharmacy database to the AWUP reported in the secondary data file and were edited, as necessary.

Beginning with the 2007 data, the rules used to identify outlier prices for prescription medications in the PC changed. New outlier thresholds were established based on the distribution of the ratio of retail unit prices relative to the AWUP in the 2006 MarketScan Outpatient Pharmaceutical Claims database. The new thresholds vary by patent status, whereas in prior years they did not. These changes improve data quality in three ways: (1) the distribution of prices in the MEPS better benchmarks to MarketScan, overall and by patent status (Zodet et al. 2010), (2) fewer pharmacy-reported payments and quantities (for example, number of pills) are edited, and (3) imputed prices reflect prices paid, rather than AWUPs. As a result, compared with earlier years of the MEPS, starting with 2007 there is more variation in prices for generics, lower mean prices for generics, higher mean prices for brand name drugs, greater differences in prices between generic and brand name drugs, and a somewhat lower proportion of spending on drugs by families, as opposed to third-party payers. Beginning with the 2008 data, pharmacy reports of free antibiotics were not edited as if they were outliers. Beginning with the 2010 data, some additional free drugs obtained through commercial pharmacies were not edited.

Beginning with the 2009 data, three changes in editing sources of payment data were made to improve data quality, based on a validation study (Hill et al., 2011). Two changes were made in editing fills for which pharmacies reported partial payment data. First, if the third party amount was missing and the third party payer was a public payer, then pharmacy reports of zero out-of-pocket amounts were preserved rather than imputed. Second, somewhat tighter outlier thresholds were implemented for the fills with partial payment data, and somewhat looser outlier thresholds were implemented for fills with complete payment data. Another change affected Medicare beneficiaries with both Part D and Medicaid coverage--reported Medicaid and other state and local program payments were no longer edited to be Medicare payments.

Beginning with the 2010 data, improvements in the payment imputation methods for pharmacy data (1) better utilize pharmacy-reported quantities to impute missing payment amounts, and (2) preserve within-NDC variation in the prices on the records for which third party payment amounts are imputed.

Drug matches between household drug mentions and pharmacy drug events for a person in the PC were based on drug code, medication name, and the round in which the drug was reported. The matching of household drug mentions to pharmacy drugs was performed so that the most detailed and accurate information for each prescribed medicine event was obtained. Beginning with the 2008 Prescribed Medicines file, the criteria for matching were changed to allow multiple NDCs for the same drug reported by pharmacies (for example, different manufacturers) to match to one drug reported by the household. Beginning with the 2010 data, the matching process was improved for diabetic supplies to better utilize pharmacy reports of the diversity of supplies individuals purchased. Exact dates of purchase were only available from the follow-back component. The matching program assigned scores to potential matches. Numeric variables required exact matches to receive a high score, while partial scores could be assigned to matches between character variables, such as prescription name, depending on the degree of similarity in the spelling and sound of the medication names. Household drug mentions that were deemed exact matches to PC drugs for the same person in the same round required sufficiently high scores to reflect a high quality match. Initially, exact matches were used only once and were taken out of the donor pool from that point on (i.e., these matches were made without replacement). Beginning with the 2008 Prescribed Medicines file, however, for remaining persons with pharmacy data from any round and unmatched household drugs, additional matches are made with replacement across rounds. Any refill of a household drug mention that had been matched to a pharmacy drug event was also matched to the same pharmacy drug event. All remaining unmatched household drug mentions for persons either in or out of the PC were statistically matched to the entire pharmacy donor base with replacement by medication name, drug code, type of third party coverage, health conditions, age, sex, and other characteristics of the individual. Potential PC donor records were omitted from these matches whenever an NDC was imputed to the PC record and was not an exact match on a generic product code applied to all records in the HC and PC. Some matches have inconsistencies between the PC donor’s potential sources of payment and those of the HC recipient, and these were resolved. Beginning with the 2008 data, the method used to resolve inconsistencies in potential payers was changed to better reflect the distribution of sources of payment among the acquisitions with consistent sources of payment. This change (1) reduced Medicare payments and increased private payments among Medicare beneficiaries, and (2) reduced out-of-pocket payments and increased Medicaid payments among Medicaid enrollees. In addition, Medicare, Medicaid, and private drug expenditures better benchmark totals in the National Health Expenditure Accounts.

For more information on the MEPS Prescribed Medicines editing and imputation procedures, please see J. Moeller, 2001.

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4.1 Rounding

Expenditure variables on the 2010 Prescribed Medicines file have been rounded to the nearest penny. Person-level expenditure variables released on the 2010 Full Year Consolidated Data File were rounded to the nearest dollar. It should be noted that using the 2010 MEPS event files to create person-level totals will yield slightly different totals than those found on the 2010 Full Year Consolidated Data File. These differences are due to rounding only. Moreover, in some instances, the number of persons having expenditures on the 2010 event files for a particular source of payment may differ from the number of persons with expenditures on the 2010 Full Year Consolidated Data File for that source of payment. This difference is also an artifact of rounding only. Please see the 2010 Appendix File, HC-135I, for details on such rounding differences.

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4.2 Edited/Imputed Expenditure Variables (RXSF10X-RXXP10X)

There are 13 expenditure variables included on this event file. All of these expenditures have gone through an editing and imputation process and have been rounded to the second decimal place. There is a sum of payments variable (RXXP10X) which, for each prescribed medicine event, sums all the expenditures from the various sources of payment. The 12 sources of payment expenditure variables for each prescribed medicine event are the following: amount paid by self or family (RXSF10X), amount paid by Medicare (RXMR10X), amount paid by Medicaid (RXMD10X), amount paid by private insurance (RXPV10X), amount paid by the Veterans Administration/CHAMPVA (RXVA10X), amount paid by TRICARE (RXTR10X), amount paid by other federal sources (RXOF10X), amount paid by state and local (non-federal) government sources (RXSL10X), amount paid by Worker’s Compensation (RXWC10X), and amount paid by some other source of insurance (RXOT10X). As mentioned previously, there are two additional expenditure variables called RXOR10X and RXOU10X (other private and other public, respectively). These two expenditure variables were created to maintain consistency between what the household respondent reported as a person’s private and public insurance status for hospitalization and physician coverage and third party prescription payments from other private and public sources (such as a separate private prescription policy or prescription coverage from the Veterans Administration, the Indian Health Service, or a State assistance program other than Medicaid). Users should exercise caution when interpreting the expenditures associated with these two additional sources of payment. While these payments stem from apparent inconsistent responses to health insurance and source of payment questions in the survey, some of these inconsistencies may have logical explanations. Please see Section 2.6.4 for details on these and all other source of payment variables.

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5.0 Strategies for Estimation

5.1 Developing Event-Level Estimates

The data in this file can be used to develop national 2010 event-level estimates for the U.S. civilian noninstitutionalized population on prescribed medicine purchases (events) as well as expenditures, and sources of payment for these purchases. Estimates of total number of purchases are the sum of the weight variable (PERWT10F) across relevant event records while estimates of other variables must be weighted by PERWT10F to be nationally representative. The tables below contain event-level estimates for selected variables.

Selected Event (Purchase) Level Estimates

All Prescribed Medicine Purchases

Estimate of Interest Variable Name Estimate (SE)
Number of purchases (in millions) PERWT10F 3273.4 (83.93)
Mean total payments per purchase RXXP10X $83 (1.7)
Mean out-of-pocket payment per purchase RXSF10X $18 (0.4)
Mean proportion of expenditures paid by private insurance per purchase RXPV10X /RXXP10X 0.171 (0.0044)

Example by Drug Type: Statins (TC1S1_1 = 173 or TC1S1_2 = 173 or TC1S2_1 = 173 or TC1S3_1 = 173 or TC2S1_1 = 173 or TC2S1_2 = 173)

Estimate of Interest Variable Name Estimate (SE)
Number of purchases (in millions) PERWT10F 233.1 (6.99)
Mean total payments per purchase RXXP10X $86 (2.7)
Mean annual total payments per person RXXP10X (aggregated across purchases within person) $505 (16.2)

Example by Associated Condition: Hypertension (RXICD1X = "401" or RXICD2X = "401" or RXICD3X = "401")

Estimate of Interest Variable Name Estimate (SE)
Number of purchases (in millions) PERWT10F 514.4 (16.24)
Mean total payments per purchase RXXP10X $40 (0.9)
Mean annual total payments per person RXXP10X (aggregated across purchases within person) $367 (9.1)

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5.2 Person-Based Estimates for Prescribed Medicine Purchases

To enhance analyses of prescribed medicine purchases, analysts may link information about prescribed medicine purchases by sample persons in this file to the annual full year consolidated file (which has data for all MEPS sample persons), or conversely, link person-level information from the full year consolidated file to this event-level file (see Section 6 below for more details). Both this file and the Full Year Consolidated File may be used to derive estimates for persons with prescribed medicine purchases and annual estimates of total expenditures for these purchases; however, if the estimate relates to the entire population, this file cannot be used to calculate the denominator, as only those persons with at least one prescribed medicine purchase are represented on this data file. Therefore, the full year consolidated file must be used for person-level analyses that include both persons with and without prescribed medicine events.

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5.3 Variables with Missing Values

It is essential that the analyst examine all variables for the presence of negative values used to represent missing values. For continuous or discrete variables, where means or totals may be taken, it may be necessary to set negative values to values appropriate to the analytic needs. That is, the analyst should either impute a value or set the value to one that will be interpreted as missing by the computing language used. For categorical and dichotomous variables, the analyst may want to consider whether to recode or impute a value for cases with negative values or whether to exclude or include such cases in the numerator and/or denominator when calculating proportions.

Methodologies used for the editing/imputation of expenditure variables (e.g., total expenditures and sources of payment) are described in Section 4.2.

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5.4 Variance Estimation (VARSTR, VARPSU)

MEPS has a complex sample design. To obtain estimates of variability (such as the standard error of sample estimates or corresponding confidence intervals) for MEPS estimates, analysts need to take into account the complex sample design of MEPS for both person-level and family-level analyses. Several methodologies have been developed for estimating standard errors for surveys with a complex sample design, including the Taylor-series linearization method, balanced repeated replication, and jackknife replication. Various software packages provide analysts with the capability of implementing these methodologies. Replicate weights have not been developed for the MEPS data. Instead, the variables needed to calculate appropriate standard errors based on the Taylor-series linearization method are included on this file as well as all other MEPS public use files. Software packages that permit the use of the Taylor-series linearization method include SUDAAN, Stata, SAS (version 8.2 and higher), and SPSS (version 12.0 and higher). For complete information on the capabilities of each package, analysts should refer to the corresponding software user documentation.

Using the Taylor-series linearization method, variance estimation strata and the variance estimation PSUs within these strata must be specified. The variance strata variable is named VARSTR, while the variance PSU variable is named VARPSU. Specifying a "with replacement" design in a computer software package, such as SUDAAN, provides standard errors appropriate for assessing the variability of MEPS survey estimates. It should be noted that the number of degrees of freedom associated with estimates of variability indicated by such a package may not appropriately reflect the actual number available. For MEPS sample estimates for characteristics generally distributed throughout the country (and thus the sample PSUs), one can expect at least 100 degrees of freedom for the 2010 full year data associated with the corresponding estimates of variance and usually substantially more.

Prior to 2002, MEPS variance strata and PSUs were developed independently from year to year, and the last two characters of the strata and PSU variable names denoted the year. However, beginning with the 2002 Point-in-Time PUF, the variance strata and PSUs were developed to be compatible with MEPS data associated with the NHIS sample design used through 2006. Such data can be pooled and the variance strata and PSU variables provided can be used without modification for variance estimation purposes for estimates covering multiple years of data.

As a result of the change in the NHIS sample design in 2006, a new set of variance strata and PSUs have been established for variance estimation purposes for use with MEPS Panel 12 and subsequent MEPS panels. There were 165 variance strata associated with both MEPS Panel 14 and Panel 15, providing a substantial number of degrees of freedom for subgroups as well as the nation as a whole. Each variance stratum contains either two or three variance estimation PSUs.

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6.0 Merging/Linking MEPS Data Files

Data from this file can be used alone or in conjunction with other files for different analytic purposes. This section summarizes various scenarios for merging/linking MEPS event files. Each MEPS panel can also be linked back to the previous year’s National Health Interview Survey public use data files. For information on obtaining MEPS/NHIS link files please see meps.ahrq.gov/data_stats/more_info_download_data_files.jsp.

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6.1 Linking to the Person-Level File

Merging characteristics of interest from the person-level file (e.g., MEPS 2010 Full Year Consolidated File) expands the scope of potential estimates. For example, to estimate the total number of prescribed medicine purchases of persons with specific demographic characteristics (such as age, race, sex, and education), population characteristics from a person-level file need to be merged onto the prescribed medicines file. This procedure is illustrated below. The MEPS 2010 Appendix File, HC-135I, provides additional detail on how to merge MEPS data files.

  1. Create data set PERSX by sorting the 2010 Full Year Consolidated File by the person identifier, DUPERSID. Keep only variables to be merged onto the prescribed medicines file and DUPERSID.
     
  2. Create data set PMEDS by sorting the 2010 Prescribed Medicines File by person identifier, DUPERSID.
     
  3. Create final data set NEWPMEDS by merging these two files by DUPERSID, keeping only records on the prescribed medicines file.

The following is an example of SAS code, which completes these steps:

PROC SORT DATA=IN.HCXXX (KEEP=DUPERSID AGE31X AGE42X AGE53X
SEX RACEX EDUCYR)
OUT=PERSX;
    BY DUPERSID;
RUN;

PROC SORT DATA=IN.HCXXXA
OUT=PMEDS;
    BY DUPERSID;
RUN;

DATA NEWPMEDS;
MERGE PMEDS (IN=A) PERSX (IN=B);
    BY DUPERSID;
        IF A;
RUN;

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6.2 Linking to the Medical Conditions File

The CLNK provides a link from MEPS event files to the 2010 Medical Conditions File. When using the CLNK, data users/analysts should keep in mind that (1) conditions are self-reported, (2) there may be multiple conditions associated with a prescribed medicine purchase, and (3) a condition may link to more than one prescribed medicine purchase or any other type of purchase. Users should also note that not all prescribed medicine purchases link to the condition file.

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6.3 Longitudinal Analysis

For Panels 1 through 8, panel-specific files (called Longitudinal Weight Files) containing estimation variables to facilitate longitudinal analysis are available for downloading in the data section of the MEPS Web site. To create longitudinal files for these panels, it is necessary to link data from two subsequent annual files that contain data for the first and second years of the panel, respectively. Starting with Panel 9, it is not necessary to link files for longitudinal analysis because Longitudinal Data Files have been constructed and are available for downloading on the Web.

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References

Cohen, S.B. (1998). Sample Design of the 1996 Medical Expenditure Panel Survey Medical Provider Component. Journal of Economic and Social Measurement, 24, 25-53.

Cohen, S.B. (1996). The Redesign of the Medical Expenditure Panel Survey: A Component of the DHHS Survey Integration Plan. Proceedings of the COPAFS Seminar on Statistical Methodology in the Public Service.

Cox, B.G. and Cohen, S.B. (1985). Imputation Procedures to Compensate for Missing Responses to Data Items. In D.B. Owen and R.G.Cornell (Eds.), Methodological Issues for Health Care Surveys (pp. 214-234). New York, NY: Marcel Dekker.

Ezzati-Rice, T.M., Rohde, F., Greenblatt, J. (2008). Sample Design of the Medical Expenditure Panel Survey Household Component, 1998–2007 (Methodology Report No. 22). Rockville, MD: Agency for Healthcare Research and Quality.

Hill, S.C., Zuvekas, S.H., and Zodet, M.W. (2011). Implications of the Accuracy of MEPS Prescription Drug Data for Health Services Research. Inquiry 48(3). Forthcoming 2011.

Moeller J.F., Stagnitti, M., Horan, E., et al. (2001). Outpatient Prescription Drugs: Data Collection and Editing in the 1996 Medical Expenditure Panel Survey (HC-010A) (MEPS Methodology Report No. 12, AHRQ Pub. No. 01-0002). Rockville, MD: Agency for Healthcare Research and Quality.

Monheit, A.C., Wilson, R., and Arnett, III, R.H. (Eds.). (1999) Informing American Health Care Policy. San Francisco, CA: Jossey-Bass Inc.

Shah, B.V., Barnwell, B.G., Bieler, G.S., Boyle, K.E., Folsom, R.E., Lavange, L., Wheeless, S.C., and Williams, R. (1996). Technical Manual: Statistical Methods and Algorithms Used in SUDAAN Release 7.0. Research Triangle Park, NC: Research Triangle Institute.

Zodet, M.W., Hill, S.C., and Miller, E. Comparison of Retail Drug Prices in the MEPS and MarketScan: Implications for MEPS Editing Rules. Agency for Healthcare Research and Quality Working Paper No. 10001, Februrary 2010.

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D. Variable-Source Crosswalk

VARIABLE-SOURCE CROSSWALK

FOR MEPS HC-135A: 2010 Prescribed Medicines Events

Survey Administration Variables

Variable Description Source
DUID Dwelling unit ID Assigned in sampling
PID Person number Assigned in sampling
DUPERSID Sample person ID (DUID + PID) Assigned in sampling
RXRECIDX Record ID – Unique Prescribed Medicine Identifier Constructed
LINKIDX Link to condition and other event files CAPI derived
DRUGIDX Link to drugs across rounds CAPI derived
PANEL Panel indicator Assigned in sampling
PURCHRD Round in which the Rx/prescribed medicine was obtained/purchased CAPI derived

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Prescribed Medicines Events Variables

Variable Description Source
RXBEGDD Day person first used medicine PM11OV2
RXBEGMM Month person first used medicine PM11OV1
RXBEGYRX Year person first used medicine PM11
RXNAME Medication name (Imputed) Imputed
RXNDC National drug code (Imputed) Imputed
RXQUANTY Quantity of Rx/prescribed medicine (Imputed) Imputed
RXFORM Form of Rx/prescribed medicine (Imputed) Imputed
RXFRMUNT Unit of measurement for form of Rx/prescribed medicine (Imputed) Imputed
RXSTRENG Strength of Rx/prescribed medicine dose (Imputed) Imputed
RXSTRUNT Unit of measurement for strength of Rx/prescribed medicine dose (Imputed) Imputed
RXDAYSUP Days supplied of prescribed med(Imputed) Imputed
PHARTP1-PHARTP7 Type of pharmacy provider – (1st-7th) PM16
RXFLG Flag variable indicating imputation source for NDC on pharmacy donor record Constructed
PCIMPFLG Flag indicating type of household to pharmacy prescription match Constructed
CLMOMFLG Charge/payment, Rx claim filing, and OMTYPE =2 or =3 (insulin and diabetic supply equipment events) status CP01/Constructed
INPCFLG Flag indicating if the person has at least one record in the pharmacy component Constructed
SAMPLE Flag indicating if a person received a free sample of this drug in the round CAPI derived
RXICD1X 3 digit ICD-9 condition code PM09
RXICD2X 3 digit ICD-9 condition code PM09
RXICD3X 3 digit ICD-9 condition code PM09
RXCCC1X Modified clinical classification code Constructed/Edited
RXCCC2X Modified clinical classification code Constructed/Edited
RXCCC3X Modified clinical classification code Constructed/Edited
PREGCAT Multum pregnancy category Cerner Multum, Inc.
TC1 Multum therapeutic class #1 Cerner Multum, Inc.
TC1S1 Multum therapeutic sub-class #1 for TC1 Cerner Multum, Inc.
TC1S1_1 Multum therapeutic sub-sub-class for TC1S1 Cerner Multum, Inc.
TC1S1_2 Multum therapeutic sub-sub-class for TC1S1 Cerner Multum, Inc.
TC1S2 Multum therapeutic sub-class #2 for TC1 Cerner Multum, Inc.
TC1S2_1 Multum therapeutic sub-sub-class for TC1S2 Cerner Multum, Inc.
TC1S3 Multum therapeutic sub-class #3 for TC1 Cerner Multum, Inc.
TC1S3_1 Multum therapeutic sub-sub-class for TC1S3 Cerner Multum, Inc.
TC2 Multum therapeutic class #2 Cerner Multum, Inc.
TC2S1 Multum therapeutic sub-class #1 for TC2 Cerner Multum, Inc.
TC2S1_1 Multum therapeutic sub-sub-class for TC2S1 Cerner Multum, Inc.
TC2S1_2 Multum therapeutic sub-sub-class for TC2S1 Cerner Multum, Inc.
TC2S2 Multum therapeutic sub-class #2 for TC2 Cerner Multum, Inc.
TC3 Multum therapeutic class #3 Cerner Multum, Inc.
TC3S1 Multum therapeutic sub-class #1 for TC3 Cerner Multum, Inc.
TC3S1_1 Multum therapeutic sub-sub-class for TC3S1 Cerner Multum, Inc.
RXSF10X Amount paid, self or family (Imputed) CP11/Edited/Imputed
RXMR10X Amount paid, Medicare (Imputed) CP12/CP13/Edited/Imputed
RXMD10X Amount paid, Medicaid (Imputed) CP12/CP13/Edited/Imputed
RXPV10X Amount paid, private insurance (Imputed) CP12/CP13/Edited/Imputed
RXVA10X Amount paid, Veteran’s Administration/CHAMPVA (Imputed) CP12/CP13/Edited/Imputed
RXTR10X Amount paid, TRICARE (Imputed) CP12/CP13/Edited/Imputed
RXOF10X Amount paid, other Federal (Imputed) CP12/CP13/Edited/Imputed
RXSL10X Amount paid, state and local government (Imputed) CP12/CP13/Edited/Imputed
RXWC10X Amount paid, Worker’s Compensation (Imputed) CP12/CP13/Edited/Imputed
RXOT10X Amount paid, other insurance (Imputed) CP12/CP13/Edited/Imputed
RXOR10X Amount paid, other private (Imputed) Constructed/Imputed
RXOU10X Amount paid, other public (Imputed) Constructed/Imputed
RXXP10X Sum of payments RXSF10X – RXOU10X (Imputed) CP12/CP13/Edited/Imputed

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Weights

Variable Description Source
PERWT10F Final person-level weight Constructed
VARSTR Variance estimation stratum, 2010 Constructed
VARPSU Variance estimation PSU, 2010 Constructed

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Appendix 1

Definitions for RXFORM, Form of Prescribed Medicines

Dosage Form Definition
-7 refused
-8 don’t know
-9 not ascertained
ACC accessory
ADR acetic acid drop
AE aerosol
AEPB aerosol powder, breath activated
AER aerosol
AER SPRAY aerosol spray
AERA aerosol with adapter
AERB aerosol, breath activated
AERO aerosol
AEROP aerosol powder
AEROSOL  
AERS aerosol, solution
AMP ampule
ARA aerosol liquid w/adapter (inhaler)
ARD aerosol solid w/adapter
ARO aerosol solid
AUTO INJ auto-injection
BACK SUPPORT BELT  
BAG  
BAL balm
BALM  
BAN bandage
BANDAGE  
BAR  
BATTERY  
BENCH  
BOT bottle
BOTTLE  
BOX  
BOXES  
BRACE  
BRIEF  
BUT butterfly
C capsules, or cream (varies)
C12 12 hour extended-release capsule
C24 24 hour extended-release capsule
CA capsule
CANE  
CAP capsule, caplets
CAP DR delayed-release capsule
CAP ER extended-release capsule
CAP SA slow-acting capsule
CAPLET  
CAPLT caplet
CAPS capsules
CAPSULE  
CAPSULE SA slow-acting capsule
CATHETER  
CC cubic centimeter
CER capsule, extended-release tablet, xtended-release
CHAMBER  
CHEW chewable tablet
CHEW TAB chewable tablet
CHEW TABS chewable tablets
CHEWABLE  
CHW chewable tablets
CLEANSER  
COLLAR  
COMBO  
COMPOUND  
CON condom
CONC concentrate
CONDOM  
CONTAINER  
COTTON  
CP12 capsule, extended-release, 12 hour
CP24 capsule, extended-release, 24 hour
CPCR capsule, extended-release
CPDR capsule, delayed release
CPEP capsule, delayed release particles
CPSP capsule sprinkle
CPSR slow-release capsule
CR cream
CRE cream
CREA cream
CREAM  
CRM cream
CRY crystal
CRYS crystals
CRYSTAL  
CTB chewable tablets
CTG cartridge
CUTTER  
DEV device
DEVI device
DEVICE  
DIA diaper
DIAPER  
DIAPHRAM  
DIS disk, or dermal infusion system
DISK  
DISKUS  
DOS PAK dose pack
DR drop
DRC delayed-release capsule
DRE dressing
DRESSING  
DRO drop
DROP  
DROPS  
DROPS OPTH OTI ophthalmic/otic drops
DROPS SUSP drops suspension
DRP drop
DRPS drops
DSK disk
DSPK tablets in a dose pack
DSPT tablet, dispersible
DT tablet, disintegrating
EAR DROP  
EAR DROPS  
EAR DRP ear drop
EAR SUSP ear suspension
EC TABS enteric coated tablets
ECC enteric coated capsules
ECT enteric coated tablets
ELI elixir
ELIX elixir
ELIXER  
ELIXIR  
ELX elixir
EMERGENCY KIT  
EMO emollient
EMU emulsion
EMUL emulsion
EMULSION  
ENE enema
ENEM enema
ENEMA  
ER  
ERC capsule, extended-release
ERSUS suspension, extended-release
ERT tablet, extended-release
ERTA extended-release-tablets
ERTC tablet, chewable, extended-release
EST  
EXTN CAP extended-release capsule
EXTRACT  
EYE DRO eye drop
EYE DROP  
EYE DROPS  
EYE DRP eye drop
EYE EMU  
EYE OIN  
EYE SO eye solution
EYEDRO  
FIL film
FILM film
FILM ER film, extended-release
FILMTAB  
FILMTABS  
FLOWMETER  
FOA foam
FOAM  
GAU gauze
GAUZE  
GEF effervescent granules
GEL  
GELC  
GEL CAP gel capsule
GELS gel-forming solution
GER granule, extended-release
GFS gel-forming solution
GLOVE  
GRA granules
GRAN granules
GRANULES  
GRAR granules for reconstitution
GRR grams
GTT drops
GUM  
HFA  
HOSE medical hosiery
HU capsule
ICR control-release insert
IMPL implant
IMPLANT  
IN injectible
INH inhalant, inhaler
INHA inhaler
INH AER inhalant aerosol
INHAL inhalant
INHAL SOL inhalant solution
INHALER  
INHL inhalant
INJ injectible
INJECTION (S)  
INSERT  
INSULIN  
IUD intrauterine devise
IV intravenous
JEL jelly
JELLY  
KI  
KIT  
L lotion
LAN  
LANCET  
LANCET (S)  
LI liquid
LINIMENT  
LIQ liquid
LIQD liquid
LIQUID  
LOLLIPOP  
LOT lotion
LOTION  
LOTN lotion
LOZ lozenge
LOZENGE  
LOZG lozenge
LQCR liquid, extended-release
MASK  
MCG microgram
METER  
MG milligram
MIS miscellaneous
MISC miscellaneous
MIST  
MONITOR  
MOUTHWASH  
NAS nasal spray
NASAL  
NASAL INHALER  
NASAL POCKET HL nasal inhaler, pocket
NASAL SOLN nasal solution
NASAL SPR nasal spray
NASAL SPRAY  
NDL needle
NE nebulizer
NEB nebulizer
NEBU nebulization solution
NEBULIZER  
NEEDLE  
NEEDLES  
NMA enema
NMO nanomole, millimicromole
NOSE DROPS  
ODR ophthalmic drop (ointment)
ODT oral disintegrating tablet
OIL  
OIN ointment
OINT ointment
OINT TOP topical ointment
OINTA ointment with applicator
OINTMENT  
ONT ointment
OP ophthalmic solution
OP DROPS ophthalmic drops
OP SOL ophthalmic solution
OPH ophthalmic
OPH S ophthalmic solution or suspension
OPH SOL ophthalmic solution
OPH SOLN ophthalmic solution
OPHT SOL ophthalmic solution
OPHTH DROP (S) ophthalmic drops
OPHTH OINT ophthalmic ointment
OPHTH SOLN ophthalmic solution
OPT SLN ophthalmic solution
OPT SOL ophthalmic solution
OPTH ophthalmic solution or suspension or ointment
OPTH S ophthalmic solution or suspension
OPTH SLN ophthalmic solution
OPTH SOL ophthalmic solution
OPTH SUSP ophthalmic suspension
OPTIC  
ORAL  
ORAL INHL oral inhalant
ORAL INHALER  
ORAL PWD oral powder
ORAL RINSE  
ORAL SOL oral solution
ORAL SUS oral suspension
ORAL SUSP oral suspension
OTHER  
OTI otic solution
OTIC  
OTIC SOL otic solution
OTIC SOLN otic solution
OTIC SUS otic suspension
OTIC SUSP otic suspension
PA tablet pack, pad or patch (varies)
PAC pack
PACK  
PAD  
PADS  
PAK pack
PAS paste
PASTE  
PAT patch
PATCH  
PATCHES  
PCH patch
PDR powder
PDS powder for reconstitution
PEDIATRIC DROPS  
PEL pellets
PEN  
PI1 powder for injection, 1 month
PI3 powder for injection, 3 months
PIH powder for inhalation
PKG package
PKT packet
PLASTER  
PLEDGETS  
PLLT pellet
PO-SYRUP syrup by mouth (oral syrup)
POPSICLE  
POUCH  
POW powder
POWD powder
POWDER  
POWDER/SUSPENS powder/suspension
PRO prophylactic
PST paste
PSTE paste
PT24 patch, 24 hour
PT72 patch, 72 hour
PTCH patch
PTTW patch, biweekly
PTWK patch, weekly
PULVULE  
PWD powder
PWD F/SOL powder for solution
PWDI powder for injection
PWDIE powder for injection, extended-release
PWDR powder for reconstitution
PWDRD powder for reconstitution, delayed-release
RCTL SUPP rectal suppository
RECTAL CREAM  
REDITABS  
REF  
RIN rinse
RING  
RINSE  
ROLL  
S syrup, suspension, solution (varies)
SA CAPS slow-acting capsules
SA TAB slow-acting tablet
SA TABLETS slow-acting tablets
SA TABS slow-acting tablets
SAL salve
SCRUB  
SER extended-release suspension
SET  
SGL soft b23gel cap
SHA shampoo
SHAM shampoo
SHMP shampoo
SHOE  
SLT sublingual tablet
SL TAB sublingual tablet
SO solution
SOA soap
SOL solution
SOLG gel forming solution
SOLN solution
SOLR solution, reconstituted
SOLUTION  
SOLU solution
SP spray
SPG sponge
SPN  
SPONGE  
SPR spray
SPRAY  
SRN syringe
ST  
STK stick
STOCKING  
STP strip
STR strip
STRIP  
STRIPS  
STRP strip
SU suspension, solution, suppository, powder,
or granules for reconstitution (varies)
SUB sublingual
SUBL tablet, sublingual
SUBLINGUAL  
SUP suppository
SUPP suppository
SUPPOSITORIES  
SUPPOSITORY  
SUS suspension
SUS/LIQ suspension/liquid
SUSP suspension
SUSPEN suspension
SUSPENDED RELEASE CAPLET  
SUSPENSION  
SUSR suspension, reconstituted
SWA swab
SWAB  
SWABS  
SYG  
SYP syrup
SYR syrup
SYRG syringe
SYRINGE  
SYRP syrup
SYRUP  
T tablet
T12 12 hour extended-release tablet
T24 24 hour extended-release tablet
TA tablet
TAB tablet
TAB CHEW chewable tablet
TAB DR delayed-release tablet
TAB EC enteric coated tablet
TAB SL Slow-acting tablet
TAB SUBL sublingual tablet
TABL tablet
TABLET  
TABLET CUTTER  
TABLET SPLITTER  
TABLETS  
TABS tablets
TAM tampon
TAP tape
TAPE  
TB tablet
TB12 tablet, extended-release 12 hour
TB24 tablet, extended-release 24 hour
TBCH chewable tablet
TBCR tablet, extended-release
TBDP tablet, dispersible
TBEC tablet, delayed-release
TBS tablets
TBSL sublingual tablet
TBSO tablet, soluble
TBSR slow-release tablet
TC tablet, chewable
TCP tablet, coated particles
TDM extended-release film
TDR orally disintegrating tablets
TDS transdermal system
TEF effervescent tablet
TER extended-release tablet
TERF film, extended-release
TES test
TEST  
TEST STRIP  
TEST STRIPS  
TIN tincture
TINC tincture
TOP CREAM topical cream
TOP OINT topical ointment
TOP SOL topical solution
TOP SOLN topical solution
TOPICAL  
TOPICAL CREAM  
TOPICAL GEL  
TOPICAL OINTMENT  
TOPICAL SOLUTION  
TRO troche
TROC troche
TROCHE  
TTB time release tablet
TUB tube
TUBE  
UNDERWEAR  
UNIT DOSE  
UNT unit
VAGINAL CREAM  
VAPORIZER  
VIA vial
VIAL  
VIAL(S)  
VIL vial
WAF wafer
WAFR wafer
WALKER  
WASH  
WIPES  
Z-PAK  

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Appendix 2

Definitions for RXFRMUNT, Unit of Measure for Form of Prescribed Medicines

Code Description
-7 refused
-8 don’t know
-9 not ascertained
CAPLT caplet
CAPS capsule
CC cubic centimeter
G gram
GM gram
GR gram
L liter
MCL microliter
MG milligram
ML milliliter
OTHER other
OZ ounce
QT quarter
TAB tablet

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Appendix 3

Definitions for RXSTRUNT, Unit of Measure for Strength of Prescribed Medicines

Abbreviations,
Codes and Symbols
Definition
-7 refused
-8 don't know
-9 not ascertained
% percent
09 compound
91 other specify
ACT actuation
ACTIVATION activation
ACTUATION actuation
BLIST blister
CC cubic centimeters
CM2 square centimeter
DOSE dose
DROP drop
DRP drop
EL ELISA (enzyme linked immunosorbent assay)
G gram
GM gram
GR grain
HR or HRS hour, hours
INH inhalation
IU international unit
MCG microgram
MEQ microequivalent
MG milligram
ML milliliter
MM millimeter
MMU millimass units
OTHER other
OZ ounce
PACKET packet
PFU plaque forming units
SPRAY spray
SQ CM square centimeter
U or UNIT units
UNT  

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Appendix 4

Definitions of Therapeutic Class Code

Therapeutic
Class Code
Definition
-9 not ascertained
-1 inapplicable
1 anti-infectives
2 amebicides
3 anthelmintics
4 antifungals
5 antimalarial agents
6 antituberculosis agents
7 antiviral agents
8 carbapenems
9 cephalosporins
10 leprostatics
11 macrolide derivatives
12 miscellaneous antibiotics
13 penicillins
14 quinolones
15 sulfonamides
16 tetracyclines
17 urinary anti-infectives
18 aminoglycosides
19 antihyperlipidemic agents
20 antineoplastics
21 alkylating agents
22 antineoplastic antibiotics
23 antimetabolites
24 antineoplastic hormones
25 miscellaneous antineoplastics
26 mitotic inhibitors
27 radiopharmaceuticals
28 biologicals
30 antitoxins and antivenins
31 bacterial vaccines
32 colony stimulating factors
33 immune globulins
34 in vivo diagnostic biologicals
36 recombinant human erythropoietins
37 toxoids
38 viral vaccines
39 miscellaneous biologicals
40 cardiovascular agents
41 agents for hypertensive emergencies
42 angiotensin converting enzyme inhibitors
43 antiadrenergic agents, peripherally acting
44 antiadrenergic agents, centrally acting
45 antianginal agents
46 antiarrhythmic agents
47 beta-adrenergic blocking agents
48 calcium channel blocking agents
49 diuretics
50 inotropic agents
51 miscellaneous cardiovascular agents
52 peripheral vasodilators
53 vasodilators
54 vasopressors
55 antihypertensive combinations
56 angiotensin II inhibitors
57 central nervous system agents
58 analgesics
59 miscellaneous analgesics
60 narcotic analgesics
61 nonsteroidal anti-inflammatory agents
62 salicylates
63 analgesic combinations
64 anticonvulsants
65 antiemetic/antivertigo agents
66 antiparkinson agents
67 anxiolytics, sedatives, and hypnotics
68 barbiturates
69 benzodiazepines
70 miscellaneous anxiolytics, sedatives and hypnotics
71 CNS stimulants
72 general anesthetics
73 muscle relaxants
74 neuromuscular blocking agents
76 miscellaneous antidepressants
77 miscellaneous antipsychotic agents
79 psychotherapeutic combinations
80 miscellaneous central nervous system agents
81 coagulation modifiers
82 anticoagulants
83 antiplatelet agents
84 heparin antagonists
85 miscellaneous coagulation modifiers
86 thrombolytics
87 gastrointestinal agents
88 antacids
89 anticholinergics/antispasmodics
90 antidiarrheals
91 digestive enzymes
92 gallstone solubilizing agents
93 GI stimulants
94 H2 antagonists
95 laxatives
96 miscellaneous GI agents
97 hormones/hormone modifiers
98 adrenal cortical steroids
99 antidiabetic agents
100 miscellaneous hormones
101 sex hormones
102 contraceptives
103 thyroid hormones
104 immunosuppressive agents
105 miscellaneous agents
106 antidotes
107 chelating agents
108 cholinergic muscle stimulants
109 local injectable anesthetics
110 miscellaneous uncategorized agents
111 psoralens
112 radiocontrast agents
113 genitourinary tract agents
114 illicit (street) drugs
115 nutritional products
116 iron products
117 minerals and electrolytes
118 oral nutritional supplements
119 vitamins
120 vitamin and mineral combinations
121 intravenous nutritional products
122 respiratory agents
123 antihistamines
124 antitussives
125 bronchodilators
126 methylxanthines
127 decongestants
128 expectorants
129 miscellaneous respiratory agents
130 respiratory inhalant products
131 antiasthmatic combinations
132 upper respiratory combinations
133 topical agents
134 anorectal preparations
135 antiseptic and germicides
136 dermatological agents
137 topical anti-infectives
138 topical steroids
139 topical anesthetics
140 miscellaneous topical agents
141 topical steroids with anti-infectives
143 topical acne agents
144 topical antipsoriatics
146 mouth and throat products
147 ophthalmic preparations
148 otic preparations
149 spermicides
150 sterile irrigating solutions
151 vaginal preparations
153 plasma expanders
154 loop diuretics
155 potassium-sparing diuretics
156 thiazide diuretics
157 carbonic anhydrase inhibitors
158 miscellaneous diuretics
159 first generation cephalosporins
160 second generation cephalosporins
161 third generation cephalosporins
162 fourth generation cephalosporins
163 ophthalmic anti-infectives
164 ophthalmic glaucoma agents
165 ophthalmic steroids
166 ophthalmic steroids with anti-infectives
167 ophthalmic anti-inflammatory agents
168 ophthalmic lubricants and irrigations
169 miscellaneous ophthalmic agents
170 otic anti-infectives
171 otic steroids with anti-infectives
172 miscellaneous otic agents
173 HMG-CoA reductase inhibitors
174 miscellaneous antihyperlipidemic agents
175 protease inhibitors
176 NRTIs
177 miscellaneous antivirals
178 skeletal muscle relaxants
179 skeletal muscle relaxant combinations
180 adrenergic bronchodilators
181 bronchodilator combinations
182 androgens and anabolic steroids
183 estrogens
184 gonadotropins
185 progestins
186 sex hormone combinations
187 miscellaneous sex hormones
191 narcotic analgesic combinations
192 antirheumatics
193 antimigraine agents
194 antigout agents
195 5HT3 receptor antagonists
196 phenothiazine antiemetics
197 anticholinergic antiemetics
198 miscellaneous antiemetics
199 hydantoin anticonvulsants
200 succinimide anticonvulsants
201 barbiturate anticonvulsants
202 oxazolidinedione anticonvulsants
203 benzodiazepine anticonvulsants
204 miscellaneous anticonvulsants
205 anticholinergic antiparkinson agents
206 miscellaneous antiparkinson agents
208 SSRI antidepressants
209 tricyclic antidepressants
210 phenothiazine antipsychotics
211 platelet aggregation inhibitors
212 glycoprotein platelet inhibitors
213 sulfonylureas
214 biguanides
215 insulin
216 alpha-glucosidase inhibitors
217 bisphosphonates
218 alternative medicines
219 nutraceutical products
220 herbal products
222 penicillinase resistant penicillins
223 antipseudomonal penicillins
224 aminopenicillins
225 beta-lactamase inhibitors
226 natural penicillins
227 NNRTIs
228 adamantane antivirals
229 purine nucleosides
230 aminosalicylates
231 nicotinic acid derivatives
232 rifamycin derivatives
233 streptomyces derivatives
234 miscellaneous antituberculosis agents
235 polyenes
236 azole antifungals
237 miscellaneous antifungals
238 antimalarial quinolines
239 miscellaneous antimalarials
240 lincomycin derivatives
241 fibric acid derivatives
242 psychotherapeutic agents
243 leukotriene modifiers
244 nasal lubricants and irrigations
245 nasal steroids
246 nasal antihistamines and decongestants
247 nasal preparations
248 topical emollients
249 antidepressants
250 monoamine oxidase inhibitors
251 antipsychotics
252 bile acid sequestrants
253 anorexiants
254 immunologic agents
256 interferons
257 immunosuppressive monoclonal antibodies
261 heparins
262 coumarins and indandiones
263 impotence agents
264 urinary antispasmodics
265 urinary pH modifiers
266 miscellaneous genitourinary tract agents
267 ophthalmic antihistamines and decongestants
268 vaginal anti-infectives
269 miscellaneous vaginal agents
270 antipsoriatics
271 thiazolidinediones
272 proton pump inhibitors
273 lung surfactants
274 cardioselective beta blockers
275 non-cardioselective beta blockers
276 dopaminergic antiparkinsonism agents
277 5-aminosalicylates
278 cox-2 inhibitors
279 gonadotropin-releasing hormone and analogs
280 thioxanthenes
281 neuraminidase inhibitors
282 meglitinides
283 thrombin inhibitors
284 viscosupplementation agents
285 factor Xa inhibitors
286 mydriatics
287 ophthalmic anesthetics
288 5-alpha-reductase inhibitors
289 antihyperuricemic agents
290 topical antibiotics
291 topical antivirals
292 topical antifungals
293 glucose elevating agents
295 growth hormones
296 inhaled corticosteroids
297 mucolytics
298 mast cell stabilizers
299 anticholinergic bronchodilators
300 corticotropin
301 glucocorticoids
302 mineralocorticoids
303 agents for pulmonary hypertension
304 macrolides
305 ketolides
306 phenylpiperazine antidepressants
307 tetracyclic antidepressants
308 SSNRI antidepressants
309 miscellaneous antidiabetic agents
310 echinocandins
311 dibenzazepine anticonvulsants
312 cholinergic agonists
313 cholinesterase inhibitors
314 antidiabetic combinations
315 glycylcyclines
316 cholesterol absorption inhibitors
317 antihyperlipidemic combinations
318 insulin-like growth factor
319 vasopressin antagonists
320 smoking cessation agents
321 ophthalmic diagnostic agents
322 ophthalmic surgical agents
323 antineoplastic monoclonal antibodies
324 antineoplastic interferons
325 sclerosing agents
327 antiviral combinations
328 antimalarial combinations
329 antituberculosis combinations
330 antiviral interferons
331 radiologic agents
332 radiologic adjuncts
333 miscellaneous iodinated contrast media
334 lymphatic staining agents
335 magnetic resonance imaging contrast media
336 non-iodinated contrast media
337 ultrasound contrast media
338 diagnostic radiopharmaceuticals
339 therapeutic radiopharmaceuticals
340 aldosterone receptor antagonists
341 atypical antipsychotics
342 renin inhibitors
343 tyrosine kinase inhibitors
344 nasal anti-infectives
345 fatty acid derivative anticonvulsants
346 gamma-aminobutyric acid reuptake inhibitors
347 gamma-aminobutyric acid analogs
348 triazine anticonvulsants
349 carbamate anticonvulsants
350 pyrrolidine anticonvulsants
351 carbonic anhydrase inhibitor anticonvulsants
352 urea anticonvulsants
353 anti-angiogenic ophthalmic agents
354 H. pylori eradication agents
355 functional bowel disorder agents
356 serotoninergic neuroenteric modulators
357 growth hormone receptor blockers
358 metabolic agents
359 peripherally acting antiobesity agents
360 lysosomal enzymes
361 miscellaneous metabolic agents
362 chloride channel activators
363 probiotics
364 antiviral chemokine receptor antagonist
365 medical gas
366 integrase strand transfer inhibitor
368 non-ionic iodinated contrast media
369 ionic iodinated contrast media
370 otic steroids
371 dipeptidyl peptidase 4 inhibitors
372 amylin analogs
373 incretin mimetics
374 cardiac stressing agents
375 peripheral opioid receptor antagonists
376 radiologic conjugating agents
377 prolactin inhibitors
378 drugs used in alcohol dependence
379 next generation cephalosporins
380 topical debriding agents
381 topical depigmenting agents
382 topical antihistamines
383 antineoplastic detoxifying agents
384 platelet-stimulating agents
385 group I antiarrhythmics
386 group II antiarrhythmics
387 group III antiarrhythmics
388 group IV antiarrhythmics
389 group V antiarrhythmics
390 hematopoietic stem cell mobilizer
391 mTOR kinase inhibitors
392 otic anesthetics
393 cerumenolytics
394 topical astringents
395 topical keratolytics
396 prostaglandin D2 antagonists
397 multikinase inhibitors
398 BCR-ABL tyrosine kinase inhibitors
399 CD52 monoclonal antibodies
400 CD33 monoclonal antibodies
401 CD20 monoclonal antibodies
402 VEGF/VEGFR inhibitors
403 mTOR inhibitors
404 EGFR inhibitors
405 HER2 inhibitors
406 glycopeptide antibiotics
407 inhaled anti-infectives
408 histone deacetylase inhibitors
409 bone resorption inhibitors
410 adrenal corticosteroid inhibitors
411 calcitonin
412 uterotonic agents
413 antigonadotropic agents
414 antidiuretic hormones
415 miscellaneous bone resorption inhibitors
416 somatostatin and somatostatin analogs
417 selective estrogen receptor modulators
418 parathyroid hormone and analogs
419 gonadotropin-releasing hormone antagonists
420 antiandrogens
422 antithyroid agents
423 aromatase inhibitors
424 estrogen receptor antagonists
426 synthetic ovulation stimulants
427 tocolytic agents
428 progesterone receptor modulators
429 trifunctional monoclonal antibodies
430 anticholinergic chronotropic agents
431 anti-CTLA-4 monoclonal antibodies
432 vaccine combinations
433 Catecholamines
435 selective phosphodiesterase-4 inhibitors
437 Immunostimulants
438 Interleukins
439 other immunostimulants
440 therapeutic vaccines
441 calcineurin inhibitors
442 TNF alfa inhibitors
443 interleukin inhibitors
444 selective immunosuppressants
445 other immunosuppressants
446 neuronal potassium channel openers
447 CD30 monoclonal antibodies
448 topical non-steroidal anti-inflammatories
449 hedgehog pathway inhibitors
450 topical antineoplastics
451 topical photochemotherapeutics
452 CFTR potentiators
453 topical rubefacient

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