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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6474352 | 7217460 | I | 6474352-5 | 20090804 | 20091123 | PER | 8049867 | UCB, INC. | 20 | YR | F | N | 20091028 | OT | UNITED STATES |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6474352 | 1012713846 | PS | CIMZIA | 1 | SUBCUTANEOUS | 400 MG SC | |||||
| 6474352 | 1012785475 | C | PREDNISONE | 1 | |||||||
| 6474352 | 1012785477 | C | ANTIBIOTICS | 2 |
Indications of drugs used
| no results found |
Outcome of event
| no results found |
Reactions reported
| Event ID | PT |
|---|---|
| 6474352 | ARTHRITIS |
| 6474352 | DIARRHOEA |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 6474352 | HP |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 6474352 | 1012713846 | 20090616 |