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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 114276032 | 11427603 | 2 | F | 20150817 | 20150827 | 20160831 | PER | US-SA-2015SA115136 | AVENTIS | 74.00 | YR | A | F | Y | 88.40000 | KG | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 114276032 | 11427603 | 1 | PS | AVAPRO | IRBESARTAN | 1 | Unknown | AVAPRO 150 MG | UNK | 20757 | 1 | DF | TABLET | ||||||
| 114276032 | 11427603 | 2 | SS | AVAPRO | IRBESARTAN | 1 | Unknown | AVAPRO 300 MG?BREAKING THE TABLET IN TWO | UNK | 20757 | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 114276032 | 11427603 | 1 | Blood pressure measurement |
| 114276032 | 11427603 | 2 | Blood pressure measurement |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 114276032 | 11427603 | Wrong technique in product usage process |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |