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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125241661 | 12524166 | 1 | I | 20160519 | 20160620 | 20160704 | 20160704 | EXP | IT-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-050594 | BRISTOL MYERS SQUIBB | 71.50 | YR | M | Y | 0.00000 | 20160704 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125241661 | 12524166 | 1 | PS | COUMADIN | WARFARIN SODIUM | 1 | Oral | 5 MG, PRN | U | 9218 | 5 | MG | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125241661 | 12524166 | 1 | Heart valve replacement |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125241661 | 12524166 | OT |
| 125241661 | 12524166 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125241661 | 12524166 | Dizziness | |
| 125241661 | 12524166 | Epistaxis | |
| 125241661 | 12524166 | Fall | |
| 125241661 | 12524166 | Head injury | |
| 125241661 | 12524166 | Pneumocephalus |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 125241661 | 12524166 | 1 | 20160101 | 0 |