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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4623939 | 5768459 | I | 4623939-0 | 20041001 | 20050324 | 20050331 | EXP | US-MERCK-0503USA04547 | MERCK HUMAN HEALTH DIVISION | M | Y | 20050331 | LW |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4623939 | 1005834852 | PS | VIOXX | 1 | ORAL | 021042 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4623939 | DS |
| 4623939 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 4623939 | ANHEDONIA |
| 4623939 | CARDIAC DISORDER |
| 4623939 | CARDIOVASCULAR DISORDER |
| 4623939 | MYOCARDIAL INFARCTION |
| 4623939 | PAIN |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |