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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4869887 | 5947073 | F | 4869887-2 | 20031208 | 20051215 | 20051230 | EXP | AU-MERCK-0512AUS00313 | MERCK HUMAN HEALTH DIVISION | 53 | YR | M | Y | 20060103 | LW | AUSTRALIA |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4869887 | 1006777322 | PS | VIOXX | 1 | ORAL | 21042 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4869887 | 1006777322 | ARTHRITIS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4869887 | DS |
| 4869887 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 4869887 | ARTERIAL THROMBOSIS |
| 4869887 | CARDIAC DISORDER |
| 4869887 | CARDIOVASCULAR DISORDER |
| 4869887 | MIGRAINE |
| 4869887 | 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 |
|---|---|---|---|---|---|
| 4869887 | 1006777322 | 20010510 | 20040930 | 1240 | DAY |