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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
4784591 | 5888978 | I | 4784591-7 | 20021101 | 20050926 | 20050930 | EXP | US-MERCK-0509USA03866 | MERCK HUMAN HEALTH DIVISION | 61 | YR | M | Y | 20050930 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
4784591 | 1006471380 | PS | VIOXX | 1 | ORAL | 021042 | |||||
4784591 | 1006471381 | SS | VIOXX | 1 | ORAL | 021042 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
4784591 | 1006471380 | BACK PAIN |
4784591 | 1006471381 | ARTHRALGIA |
Outcome of event
Event ID | OUTC COD |
---|---|
4784591 | OT |
Reactions reported
Event ID | PT |
---|---|
4784591 | ACUTE CORONARY SYNDROME |
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 |
---|---|---|---|---|---|
4784591 | 1006471380 | 20010401 | 20021201 | 21 | MON |
4784591 | 1006471381 | 20010401 | 20021201 | 21 | MON |