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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126664941 | 12666494 | 1 | I | 20160804 | 20160819 | 20160819 | EXP | US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-066543 | BRISTOL MYERS SQUIBB | 47.00 | YR | M | Y | 0.00000 | 20160819 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126664941 | 12666494 | 1 | PS | WARFARIN SODIUM. | WARFARIN SODIUM | 1 | Oral | 10 MG, UNK | 9218 | 10 | MG | ||||||||
| 126664941 | 12666494 | 2 | SS | PHENYTOIN. | PHENYTOIN | 1 | Oral | 400 MG, QD | 0 | 400 | MG | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126664941 | 12666494 | 1 | Deep vein thrombosis |
| 126664941 | 12666494 | 2 | Seizure |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126664941 | 12666494 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126664941 | 12666494 | International normalised ratio fluctuation | |
| 126664941 | 12666494 | Labelled drug-drug interaction medication error |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |