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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
4913910 | 5985991 | F | 4913910-3 | 20040401 | 20050829 | 20060216 | EXP | US-MERCK-0508USA04856 | MERCK HUMAN HEALTH DIVISION | 80 | YR | F | Y | 20060216 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
4913910 | 1006943605 | PS | VIOXX | 1 | ORAL | 021042 | |||||
4913910 | 1006943606 | SS | VIOXX | 1 | ORAL | 021042 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
4913910 | 1006943605 | ARTHRITIS |
4913910 | 1006943606 | ARTHRALGIA |
Outcome of event
Event ID | OUTC COD |
---|---|
4913910 | OT |
Reactions reported
Event ID | PT |
---|---|
4913910 | CARDIAC DISORDER |
4913910 | CEREBROVASCULAR ACCIDENT |
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 |
---|---|---|---|---|---|
4913910 | 1006943605 | 20020101 | 20040101 | ||
4913910 | 1006943606 | 20020101 | 20040101 |