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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4830809 | 5828676 | F | 4830809-1 | 20030501 | 20050623 | 20051117 | EXP | US-MERCK-0506USA03567 | MERCK HUMAN HEALTH DIVISION | 66 | YR | M | Y | 82 | KG | 20051118 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4830809 | 1006635451 | PS | VIOXX | 1 | ORAL | 021042 | |||||
| 4830809 | 1006635452 | C | ATENOLOL | 2 | UNKNOWN |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4830809 | 1006635451 | OSTEOARTHRITIS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4830809 | DS |
| 4830809 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 4830809 | ACUTE MYOCARDIAL INFARCTION |
| 4830809 | CARDIAC FAILURE CONGESTIVE |
| 4830809 | CORONARY ARTERY DISEASE |
| 4830809 | DYSPNOEA |
| 4830809 | HEAD DISCOMFORT |
| 4830809 | ROTATOR CUFF SYNDROME |
| 4830809 | 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 |
|---|---|---|---|---|---|
| 4830809 | 1006635451 | 20010503 | 20040501 |