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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4623944 | 5768463 | I | 4623944-4 | 20041201 | 20050324 | 20050331 | EXP | US-MERCK-0503USA04467 | MERCK HUMAN HEALTH DIVISION | 57 | YR | F | Y | 20050331 | PH |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4623944 | 1005834859 | PS | VIOXX | 1 | ORAL | 021042 | |||||
| 4623944 | 1005834860 | C | [THERAPY UNSPECIFIED] | 2 | UNKNOWN |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4623944 | 1005834859 | ARTHRITIS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4623944 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 4623944 | ACCIDENT |
| 4623944 | FEMUR FRACTURE |
| 4623944 | PAIN |
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 |
|---|---|---|---|---|---|
| 4623944 | 1005834859 | 20000101 |