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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127421051 | 12742105 | 1 | I | 20160901 | 20160914 | 20160914 | EXP | US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-074074 | BRISTOL MYERS SQUIBB | 70.00 | YR | F | Y | 0.00000 | 20160914 | OT | US | US |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127421051 | 12742105 | 1 | PS | WARFARIN SODIUM. | WARFARIN SODIUM | 1 | Unknown | 2 MG, QD | 9218 | 2 | MG | QD | |||||||
| 127421051 | 12742105 | 2 | SS | WARFARIN SODIUM. | WARFARIN SODIUM | 1 | Unknown | 24 MG, QWK | 9218 | 24 | MG | /wk | |||||||
| 127421051 | 12742105 | 3 | SS | WARFARIN SODIUM. | WARFARIN SODIUM | 1 | Unknown | 56 MG, QWK | 9218 | 56 | MG | /wk | |||||||
| 127421051 | 12742105 | 4 | SS | WARFARIN SODIUM. | WARFARIN SODIUM | 1 | Unknown | 32 MG, QWK | 9218 | 32 | MG | /wk | |||||||
| 127421051 | 12742105 | 5 | SS | WARFARIN SODIUM. | WARFARIN SODIUM | 1 | Unknown | 40 MG, QWK | 9218 | 40 | MG | /wk | |||||||
| 127421051 | 12742105 | 6 | SS | WARFARIN SODIUM. | WARFARIN SODIUM | 1 | Unknown | 38 MG, QWK | 9218 | 38 | MG | /wk |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127421051 | 12742105 | 1 | Atrial fibrillation |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127421051 | 12742105 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127421051 | 12742105 | Coagulation factor VII level decreased | |
| 127421051 | 12742105 | Contraindicated product administered | |
| 127421051 | 12742105 | Incorrect dosage administered | |
| 127421051 | 12742105 | International normalised ratio increased | |
| 127421051 | 12742105 | Vaginal haemorrhage |
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 |
|---|---|---|---|---|---|---|
| 127421051 | 12742105 | 1 | 20110411 | 0 | ||
| 127421051 | 12742105 | 4 | 20140811 | 0 | ||
| 127421051 | 12742105 | 5 | 20141007 | 0 |