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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123706494 | 12370649 | 4 | F | 20160713 | 20160516 | 20160713 | PER | US-009507513-1605USA004509 | MERCK | 47.00 | YR | F | Y | 0.00000 | 20160713 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123706494 | 12370649 | 1 | PS | COZAAR | LOSARTAN POTASSIUM | 1 | Oral | 25 MG, UNK | L046902 | 20386 | 25 | MG | TABLET | ||||||
| 123706494 | 12370649 | 2 | SS | COZAAR | LOSARTAN POTASSIUM | 1 | Oral | 25 MG, UNK | L046902 | 20386 | 25 | MG | TABLET | ||||||
| 123706494 | 12370649 | 3 | SS | COZAAR | LOSARTAN POTASSIUM | 1 | Oral | 25 MG, UNK | M013215 | 20386 | 25 | MG | TABLET |
Indications of drugs used
| no results found |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 123706494 | 12370649 | Chest pain | |
| 123706494 | 12370649 | Dizziness | |
| 123706494 | 12370649 | Palpitations |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |