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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6484016 | 7230811 | I | 6484016-X | 20090701 | 20090918 | 20091123 | PER | 8052444 | UCB, INC. | 28 | YR | F | N | 20091030 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6484016 | 1012749346 | PS | CIMZIA | 1 | SUBCUTANEOUS | 200 MG 1/2W SC | D | D | 51384 | 20091001 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6484016 | 1012749346 | CROHN'S DISEASE |
Outcome of event
| no results found |
Reactions reported
| Event ID | PT |
|---|---|
| 6484016 | PREGNANCY |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 6484016 | HP |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 6484016 | 1012749346 | 20090217 | 20090901 |