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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 8626050 | 8735056 | F | 8626050-7 | 20101201 | 20120824 | 20120827 | EXP | BR-ABBOTT-12P-020-0969954-00 | ABBOTT | 31 | YR | F | Y | 56.5 | KG | 20120827 | CN | BRAZIL |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 8626050 | 1020680071 | SS | HUMIRA | 1 | SUBCUTANEOUS | UNKNOWN | |||||
| 8626050 | 1020680070 | SS | HUMIRA | 1 | SUBCUTANEOUS | UNKNOWN | |||||
| 8626050 | 1020680069 | PS | HUMIRA | 1 | SUBCUTANEOUS | UNKNOWN | |||||
| 8626050 | 1020680072 | C | CELESTAMINE TAB | 1 | 1 TABLET IN THE DAYS OF HUMIRA INJECTIONS |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 8626050 | 1020680069 | CROHN'S DISEASE |
| 8626050 | 1020680072 | INJECTION RELATED REACTION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 8626050 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 8626050 | ABORTION SPONTANEOUS |
| 8626050 | INJECTION SITE WARMTH |
| 8626050 | INJECTION SITE ERYTHEMA |
| 8626050 | PAIN IN EXTREMITY |
| 8626050 | INJECTION SITE SWELLING |
| 8626050 | INJECTION SITE INDURATION |
| 8626050 | INTESTINAL PERFORATION |
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 |
|---|---|---|---|---|---|
| 8626050 | 1020680071 | 20100901 | 20100901 | ||
| 8626050 | 1020680070 | 20100901 | 20100901 | ||
| 8626050 | 1020680069 | 20100901 | |||
| 8626050 | 1020680072 | 20120401 |