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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4784594 | 5888980 | I | 4784594-2 | 20020101 | 20050923 | 20050930 | EXP | IT-MERCK-0509ITA00033 | MERCK HUMAN HEALTH DIVISION | M | Y | 20050930 | CN | ITALY |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4784594 | 1006471384 | PS | VIOXX | 1 | ORAL | 021042 | |||||
| 4784594 | 1006471385 | SS | VIOXX | 1 | ORAL | 021042 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4784594 | 1006471384 | OSTEOARTHRITIS |
| 4784594 | 1006471385 | BACK PAIN |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4784594 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 4784594 | 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 |
|---|---|---|---|---|---|
| 4784594 | 1006471384 | 20010101 | 20020101 | 366 | DAY |
| 4784594 | 1006471385 | 20010101 | 20020101 | 366 | DAY |