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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4784596 | 5888982 | I | 4784596-6 | 20040401 | 20050926 | 20050930 | EXP | US-MERCK-0509USA03864 | MERCK HUMAN HEALTH DIVISION | 62 | YR | F | Y | 20050930 | LW | 20040405 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4784596 | 1006471387 | PS | VIOXX | 1 | ORAL | 021042 | |||||
| 4784596 | 1006471388 | SS | VIOXX | 1 | ORAL | 021042 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4784596 | 1006471387 | INTERVERTEBRAL DISC DEGENERATION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4784596 | DE |
| 4784596 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 4784596 | ACUTE 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 |
|---|---|---|---|---|---|
| 4784596 | 1006471387 | 20011201 | |||
| 4784596 | 1006471388 | 20011201 | 20040401 |