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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5374685 | 6345758 | I | 5374685-X | 20070525 | 20070620 | 20070629 | EXP | FR-JNJFOC-20070604889 | CENTOCOR PHARMACOVIGILANCE | M | Y | 86 | KG | 20070629 | MD | FRANCE |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5374685 | 1008646767 | PS | REMICADE | 1 | INTRAVENOUS | ||||||
| 5374685 | 1008646768 | C | AZATHIOPRINE SODIUM | 1 | |||||||
| 5374685 | 1008646769 | C | SOLU-MEDROL | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5374685 | 1008646767 | CROHN'S DISEASE |
| 5374685 | 1008646768 | CROHN'S DISEASE |
| 5374685 | 1008646769 | CROHN'S DISEASE |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5374685 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 5374685 | DERMATOMYOSITIS |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |