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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
7205771 | 7717331 | F | 7205771-7 | 20101221 | 20101231 | EXP | US-BRISTOL-MYERS SQUIBB COMPANY-15436488 | BRISTOL-MYERS SQUIBB COMPANY | 7 | DEC | F | Y | 20101231 | MD | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
7205771 | 1015450443 | PS | ONGLYZA | 1 | 5 MG TAB SPLIT TO 2.5 MG DOSE | 022350 |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
7205771 | HO |
Reactions reported
Event ID | PT |
---|---|
7205771 | PANCREATITIS |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |