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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4369008 | 4151964 | I | 4369008-9 | 20030530 | 20040511 | 20040525 | EXP | GB-JNJFOC-20040501840 | CENTOCOR, INC | 67 | YR | F | N | 20040524 | OT |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4369008 | 1004909732 | PS | REMICADE | 1 | INTRAVENOUS | 200 MG, INTRAVENOUS | D | D | |||
| 4369008 | 1004926497 | C | DEPO-MEDROL | 1 | |||||||
| 4369008 | 1004926500 | C | BENDROFLUAZIDE (BENDROFLUMETHIAZIDE) | 2 | |||||||
| 4369008 | 1004926502 | C | CO-PROXAMOL (APOREX) | 2 | |||||||
| 4369008 | 1004926503 | C | PREDNISOLONED (PREDNISOLONE) | 2 | |||||||
| 4369008 | 1004926504 | C | METHOTREXATE | 1 | |||||||
| 4369008 | 1004926507 | C | FOLIC ACID | 1 | |||||||
| 4369008 | 1004926508 | C | HRT (ANDROGENS AND FEMALE SEX HORMONES IN COMB) | 2 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4369008 | 1004909732 | RHEUMATOID ARTHRITIS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4369008 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 4369008 | UPPER LIMB FRACTURE |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4369008 | FGN |
| 4369008 | HP |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 4369008 | 1004909732 | 20030513 |