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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4747389 | 5789107 | F | 4747389-1 | 20020515 | 20050428 | 20050817 | EXP | US-MERCK-0505USA00240 | MERCK HUMAN HEALTH DIVISION | 67 | YR | F | Y | 112 | KG | 20050818 | OT | UNITED STATES |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4747389 | 1006330579 | PS | VIOXX | 1 | ORAL | 21042 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4747389 | HO |
| 4747389 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 4747389 | CEREBROVASCULAR ACCIDENT |
| 4747389 | CHEST PAIN |
| 4747389 | TRANSIENT ISCHAEMIC ATTACK |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 4747389 | 1006330579 | 20020101 | 20040901 | 32 | MON |