The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
127045241 12704524 1 I 20151108 20151111 20160831 20160831 PER US-SA-2015SA183797 AVENTIS 75.00 YR E F Y 0.00000 20160831 CN US US

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
127045241 12704524 1 PS AVAPRO IRBESARTAN 1 Unknown N GE227 20757 .5 DF FILM-COATED TABLET QD
127045241 12704524 2 SS AVAPRO IRBESARTAN 1 Unknown N UNKNOWN 20757 150 MG FILM-COATED TABLET
127045241 12704524 3 SS AVAPRO IRBESARTAN 1 Unknown N UNKNOWN 20757 300 MG FILM-COATED TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127045241 12704524 1 Blood pressure measurement
127045241 12704524 2 Blood pressure measurement
127045241 12704524 3 Blood pressure measurement

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127045241 12704524 Blood pressure increased
127045241 12704524 Drug ineffective
127045241 12704524 Weight decreased

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
127045241 12704524 1 20151108 0
127045241 12704524 2 2005 0