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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
4960037 | 6017023 | F | 4960037-0 | 20060202 | 20060331 | EXP | US-MERCK-0603USA04294 | MERCK HUMAN HEALTH DIVISION | M | Y | 20060403 | CN | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
4960037 | 1007119004 | PS | VIOXX | 1 | UNKNOWN | 021042 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
4960037 | 1007119004 | ARTHRITIS |
Outcome of event
Event ID | OUTC COD |
---|---|
4960037 | DE |
Reactions reported
Event ID | PT |
---|---|
4960037 | DEATH |
4960037 | MYOCARDIAL INFARCTION |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |