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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5795038 | 6686840 | F | 5795038-6 | 20080506 | 20080630 | PER | US-BRISTOL-MYERS SQUIBB COMPANY-14110746 | BRISTOL-MYERS SQUIBB COMPANY | F | Y | 20080630 | CN | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5795038 | 1010110886 | PS | ORENCIA | 1 | |||||||
5795038 | 1010110887 | SS | METHOTREXATE | 1 | 086358 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
5795038 | 1010110886 | RHEUMATOID ARTHRITIS |
Outcome of event
no results found |
Reactions reported
Event ID | PT |
---|---|
5795038 | ALOPECIA |
5795038 | WHITE BLOOD CELL COUNT DECREASED |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |