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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5001495 | 6044773 | I | 5001495-5 | 20040401 | 20060503 | 20060512 | EXP | US-MERCK-0605USA00865 | MERCK HUMAN HEALTH DIVISION | 60 | YR | M | Y | 68 | KG | 20060515 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5001495 | 1007281965 | PS | VIOXX | 1 | ORAL | 021042 | |||||
5001495 | 1007281966 | C | ALEVE (CAPLET) | 1 | UNKNOWN |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
5001495 | 1007281965 | ARTHRITIS |
Outcome of event
Event ID | OUTC COD |
---|---|
5001495 | HO |
Reactions reported
Event ID | PT |
---|---|
5001495 | 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 |
---|---|---|---|---|---|
5001495 | 1007281965 | 20040201 | 20041101 | 8 | MON |