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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4880509 | 5721894 | F | 4880509-7 | 20020601 | 20050114 | 20060113 | EXP | US-MERCK-0501USA03379 | MERCK HUMAN HEALTH DIVISION | 50 | YR | M | Y | 95 | KG | 20060117 | LW | 20030107 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4880509 | 1006819777 | PS | VIOXX | 1 | ORAL | 21042 | |||||
| 4880509 | 1006819778 | SS | VIOXX | 1 | ORAL | 021042 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4880509 | 1006819777 | ARTHRITIS |
| 4880509 | 1006819778 | SHOULDER PAIN |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4880509 | DE |
Reactions reported
| Event ID | PT |
|---|---|
| 4880509 | ARTERIOSCLEROSIS |
| 4880509 | CARDIOMEGALY |
| 4880509 | CONGESTIVE CARDIOMYOPATHY |
| 4880509 | CORONARY ARTERY OCCLUSION |
| 4880509 | INTERSTITIAL LUNG DISEASE |
| 4880509 | MYOCARDIAL FIBROSIS |
| 4880509 | MYOCARDIAL INFARCTION |
| 4880509 | PERICARDIAL HAEMORRHAGE |
| 4880509 | TOOTH DISORDER |
| 4880509 | VENTRICULAR FIBRILLATION |
| 4880509 | VENTRICULAR TACHYCARDIA |
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 |
|---|---|---|---|---|---|
| 4880509 | 1006819777 | 20021121 | 20030707 | 229 | DAY |
| 4880509 | 1006819778 | 20021121 | 20030707 | 229 | DAY |