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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6387684 | 7149207 | I | 6387684-6 | 20090910 | 20090918 | 20090930 | EXP | 8052301 | UCB, INC. | 38 | YR | F | N | 47.7 | KG | 20090928 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6387684 | 1012374641 | PS | CIMZIA | 1 | SUBCUTANEOUS | 400 MG SC | D | D | |||
| 6387684 | 1012429580 | C | LEXAPRO | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6387684 | 1012374641 | CROHN'S DISEASE |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6387684 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 6387684 | EATING DISORDER |
| 6387684 | PAIN |
| 6387684 | WEIGHT DECREASED |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 6387684 | CSM |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 6387684 | 1012374641 | 20090701 |