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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6387685 | 7125434 | F | 1 | 6387685-8 | 20090709 | 20090918 | 20090930 | EXP | 8051104 | UCB, INC. | 41 | F | N | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6387685 | 1012374643 | PS | CIMZIA | 1 | SUBCUTANEOUS | 200 MG 1/2W SC | D | D | CTD036 | 20120101 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6387685 | 1012374643 | CROHN'S DISEASE |
Outcome of event
Event ID | OUTC COD |
---|---|
6387685 | HO |
Reactions reported
Event ID | PT |
---|---|
6387685 | ABDOMINAL INFECTION |
6387685 | SMALL INTESTINAL RESECTION |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
6387685 | HP |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
6387685 | 1012374643 | 20090106 |