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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125257632 | 12525763 | 2 | F | 20160728 | 20160705 | 20160811 | EXP | FR-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-053647 | BRISTOL MYERS SQUIBB | 4.00 | YR | Y | 0.00000 | 20160811 | OT | FR | FR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125257632 | 12525763 | 1 | PS | WARFARIN SODIUM. | WARFARIN SODIUM | 1 | Unknown | 3 MG, QD | Y | 9218 | 3 | MG | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125257632 | 12525763 | 1 | Stent placement |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125257632 | 12525763 | OT |
| 125257632 | 12525763 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125257632 | 12525763 | Compartment syndrome | |
| 125257632 | 12525763 | Drug administered to patient of inappropriate age | |
| 125257632 | 12525763 | Haematoma | |
| 125257632 | 12525763 | International normalised ratio increased | |
| 125257632 | 12525763 | Overdose | |
| 125257632 | 12525763 | Prothrombin time shortened | |
| 125257632 | 12525763 | Surgery |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |