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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5000912 | 5769262 | F | 5000912-4 | 20000101 | 20050324 | 20060512 | EXP | US-MERCK-0503USA04786 | MERCK HUMAN HEALTH DIVISION | 74 | YR | M | Y | 127 | KG | 20060512 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5000912 | 1007279385 | PS | VIOXX | 1 | ORAL | 21042 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5000912 | 1007279385 | ARTHRITIS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5000912 | DS |
| 5000912 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 5000912 | ANGINA UNSTABLE |
| 5000912 | ARTHRITIS |
| 5000912 | ASPARTATE AMINOTRANSFERASE INCREASED |
| 5000912 | ASTHMA |
| 5000912 | BACK PAIN |
| 5000912 | BLOOD PRESSURE DECREASED |
| 5000912 | CARDIAC FAILURE |
| 5000912 | CORONARY ARTERY DISEASE |
| 5000912 | COUGH |
| 5000912 | DIARRHOEA |
| 5000912 | DIFFICULTY IN WALKING |
| 5000912 | DIVERTICULITIS |
| 5000912 | DYSPNOEA |
| 5000912 | ENCEPHALOPATHY |
| 5000912 | GASTROENTERITIS |
| 5000912 | HIATUS HERNIA |
| 5000912 | MUSCULOSKELETAL CHEST PAIN |
| 5000912 | MYOCARDIAL INFARCTION |
| 5000912 | NAUSEA |
| 5000912 | PAIN IN EXTREMITY |
| 5000912 | SINUSITIS |
| 5000912 | SPINAL DISORDER |
| 5000912 | VOMITING |
| 5000912 | WEIGHT DECREASED |
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 |
|---|---|---|---|---|---|
| 5000912 | 1007279385 | 20000101 | 20040930 |