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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125207591 | 12520759 | 1 | I | 201606 | 20160627 | 20160701 | 20160701 | EXP | VN-009507513-1606VNM012986 | MERCK | 78.00 | YR | M | Y | 0.00000 | 20160701 | CN | VN | VN |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125207591 | 12520759 | 1 | PS | COZAAR | LOSARTAN POTASSIUM | 1 | Oral | STRENGTH 50 MG, ONCE TABLET, ONCE A DAY | 20386 | 50 | MG | FILM-COATED TABLET | QD |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125207591 | 12520759 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125207591 | 12520759 | Blood pressure decreased | |
| 125207591 | 12520759 | Fatigue | |
| 125207591 | 12520759 | Heart rate decreased | |
| 125207591 | 12520759 | Loss of consciousness |
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 |
|---|---|---|---|---|---|---|
| 125207591 | 12520759 | 1 | 20150828 | 0 |