Person who experienced the adverse event (patient)
| Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5903983 | 6775699 | I | 5903983-3 | 20080328 | 20080930 | EXP | AT-MERCK-0809AUT00007 | MERCK HUMAN HEALTH DIVISION | M | Y | 20080930 | MD | AUSTRIA |
Drug(s) used by person
| Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5903983 | 1010522448 | PS | COZAAR | 1 | ORAL | 020386 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5903983 | 1010522448 | HYPERTENSION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5903983 | DE |
Reactions reported
| Event ID | PT |
|---|---|
| 5903983 | CEREBROVASCULAR ACCIDENT |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |