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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
95142282 | 9514228 | 2 | F | 201305 | 20150916 | 20130910 | 20160831 | PER | US-SANOFI-AVENTIS-BMS19033448 | AVENTIS | 62.00 | YR | A | M | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
95142282 | 9514228 | 1 | PS | AVAPRO | IRBESARTAN | 1 | Unknown | Y | UNK | 20757 | 150 | MG | QD | ||||||
95142282 | 9514228 | 2 | SS | IRBESARTAN WINTHROP | IRBESARTAN | 1 | Unknown | Y | UNK | 20757 | 150 | MG | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
95142282 | 9514228 | 1 | Hypertension |
95142282 | 9514228 | 2 | Hypertension |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
95142282 | 9514228 | Drug ineffective | |
95142282 | 9514228 | Hypertension |
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 |
---|---|---|---|---|---|---|
95142282 | 9514228 | 1 | 20130527 | 0 | ||
95142282 | 9514228 | 2 | 201305 | 0 |