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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127045721 | 12704572 | 1 | I | 201604 | 20160412 | 20160831 | 20160831 | PER | US-SA-2016SA075623 | AVENTIS | 76.00 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127045721 | 12704572 | 1 | PS | AVAPRO | IRBESARTAN | 1 | N | Y | HB076 | 20757 | 300 | MG | FILM-COATED TABLET | QD | |||||
127045721 | 12704572 | 2 | SS | AVAPRO | IRBESARTAN | 1 | N | Y | HB076 | 20757 | 150 | MG | FILM-COATED TABLET | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127045721 | 12704572 | 1 | Hypertension |
127045721 | 12704572 | 2 | Hypertension |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127045721 | 12704572 | Balance disorder | |
127045721 | 12704572 | Burning sensation | |
127045721 | 12704572 | Dizziness | |
127045721 | 12704572 | Hypertension | |
127045721 | 12704572 | Pain | |
127045721 | 12704572 | Product use issue | |
127045721 | 12704572 | Rash | Rash |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |