Person who experienced the adverse event (patient)
Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126715221 | 12671522 | 1 | I | 20101228 | 20160808 | 20160822 | 20160822 | EXP | IT-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-065397 | BRISTOL MYERS SQUIBB | 30.28 | YR | F | Y | 0.00000 | 20160822 | CN | IT | IT |
Drug(s) used by person
Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126715221 | 12671522 | 1 | PS | COUMADIN | WARFARIN SODIUM | 1 | Oral | U | 9218 | TABLET |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126715221 | 12671522 | 1 | Cerebral ischaemia |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126715221 | 12671522 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126715221 | 12671522 | Asthenia | |
126715221 | 12671522 | Menometrorrhagia | |
126715221 | 12671522 | Metrorrhagia | |
126715221 | 12671522 | Pallor |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |