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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5374684 | 6345757 | I | 5374684-8 | 20070510 | 20070619 | 20070629 | EXP | SE-JNJFOC-20070604879 | CENTOCOR PHARMACOVIGILANCE | F | Y | 60.3 | KG | 20070629 | MD | SWEDEN |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5374684 | 1008646764 | PS | REMICADE | 1 | INTRAVENOUS | ||||||
| 5374684 | 1008646765 | C | TENORMIN | 1 | ORAL | ||||||
| 5374684 | 1008646766 | C | PREDNISOLONE | 1 | ORAL |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5374684 | 1008646764 | RHEUMATOID ARTHRITIS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5374684 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5374684 | SYNOVITIS |
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 |
|---|---|---|---|---|---|
| 5374684 | 1008646765 | 20030101 | |||
| 5374684 | 1008646766 | 20070208 |