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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
4387950 | 4162427 | F | 4387950-X | 20020101 | 20030929 | 20040630 | EXP | US-MERCK-0310USA00073 | MERCK HUMAN HEALTH DIVISION | 20 | YR | M | Y | 95 | KG | 20040701 | CN |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
4387950 | 1004981123 | C | CELEBREX | 1 | UNKNOWN | ||||||
4387950 | 1004981124 | PS | VIOXX | 1 | ORAL | ||||||
4387950 | 1004981125 | SS | VIOXX | 1 | ORAL |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
4387950 | 1004981124 | ARTHRALGIA |
4387950 | 1004981125 | ARTHRITIS |
Outcome of event
Event ID | OUTC COD |
---|---|
4387950 | DS |
4387950 | OT |
Reactions reported
Event ID | PT |
---|---|
4387950 | ARTHROPATHY |
4387950 | CONVULSION |
4387950 | EMOTIONAL DISTRESS |
4387950 | HEADACHE |
4387950 | INTRACRANIAL ANEURYSM |
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 |
---|---|---|---|---|---|
4387950 | 1004981124 | 20020101 | 20020101 | ||
4387950 | 1004981125 | 20020101 | 20020101 |