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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6523912 | 7235222 | I | 6523912-1 | 20091209 | 20091223 | 20091231 | EXP | CA-ABBOTT-09P-028-0616239-00 | ABBOTT LABORATORIES | 25 | F | Y | 56.75 | KG | 20091231 | CANADA |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6523912 | 1012888030 | PS | HUMIRA | 1 | SUBCUTANEOUS | UNKNOWN |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6523912 | 1012888030 | CROHN'S DISEASE |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6523912 | HO |
| 6523912 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 6523912 | ABDOMINAL PAIN LOWER |
| 6523912 | ABSCESS INTESTINAL |
| 6523912 | FEELING OF BODY TEMPERATURE CHANGE |
| 6523912 | RASH |
| 6523912 | WEIGHT DECREASED |
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 |
|---|---|---|---|---|---|
| 6523912 | 1012888030 | 20081212 |