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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
7915604 | 8245625 | I | 7915604-9 | 20110907 | 20111115 | PER | US-BRISTOL-MYERS SQUIBB COMPANY-15863616 | BRISTOL-MYERS SQUIBB COMPANY | YR | F | Y | 20111115 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
7915604 | 1018052475 | PS | YERVOY | 1 |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
7915604 | OT |
Reactions reported
Event ID | PT |
---|---|
7915604 | ABDOMINAL PAIN |
7915604 | FREQUENT BOWEL MOVEMENTS |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |