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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4223542 | 3886288 | F | 1 | 4223542-0 | 20021028 | 20031020 | 20031029 | EXP | NSADSS2002046027 | CENTOCOR, INC. | 20 | YR | M | N | 20031028 | MD |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4223542 | 1004334703 | PS | REMICADE | 1 | 300 MG, 1 IN 1 DAY | U | U | ||||
| 4223542 | 1004376198 | C | BENADRYL | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4223542 | 1004334703 | CROHN'S DISEASE |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4223542 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 4223542 | ARTHRALGIA |
| 4223542 | DIZZINESS |
| 4223542 | DYSPNOEA |
| 4223542 | HOT FLUSH |
| 4223542 | MUSCULOSKELETAL STIFFNESS |
| 4223542 | TRISMUS |
| 4223542 | TYPE IV HYPERSENSITIVITY REACTION |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4223542 | FGN |
| 4223542 | HP |
Therapies reported
| no results found |