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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4869883 | 5927530 | F | 4869883-5 | 20021021 | 20051115 | 20051230 | EXP | US-MERCK-0511USA02493 | MERCK HUMAN HEALTH DIVISION | 53 | YR | F | Y | 100 | KG | 20060103 | LW | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4869883 | 1006777306 | PS | VIOXX | 1 | ORAL | 21042 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4869883 | 1006777306 | ARTHRITIS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4869883 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 4869883 | MYOCARDIAL INFARCTION |
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 |
|---|---|---|---|---|---|
| 4869883 | 1006777306 | 20000101 | 20040101 |