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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6489071 | 7231239 | I | 6489071-9 | 20091003 | 20091008 | 20091123 | PER | 8053116 | UCB, INC. | F | N | 60.7 | KG | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6489071 | 1012762441 | PS | CIMZIA | 1 | SUBCUTANEOUS | 400 MG SC | D | D | 52081 | 20101001 | |
6489071 | 1012865639 | SS | MERCAPTOPURINE | 1 | ORAL | 50 MG /D PO | D | D |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6489071 | 1012762441 | CROHN'S DISEASE |
Outcome of event
no results found |
Reactions reported
Event ID | PT |
---|---|
6489071 | DIARRHOEA HAEMORRHAGIC |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
6489071 | HP |
Therapies reported
no results found |