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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4870776 | 5954216 | F | 4870776-8 | 20020101 | 20051005 | 20060103 | EXP | US-MERCK-0510USA04109 | MERCK HUMAN HEALTH DIVISION | 63 | YR | M | Y | 107 | KG | 20060103 | LW | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4870776 | 1006781448 | PS | VIOXX | 1 | ORAL | 021042 | |||||
| 4870776 | 1006781449 | C | NORVASC | 1 | UNKNOWN | ||||||
| 4870776 | 1006781450 | C | INDOMETHACIN | 2 | UNKNOWN |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4870776 | 1006781448 | PAIN |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4870776 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 4870776 | CARDIAC DISORDER |
| 4870776 | HAEMORRHAGE |
| 4870776 | 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 |
|---|---|---|---|---|---|
| 4870776 | 1006781448 | 20000101 | 20020101 |