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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 69574934 | 6957493 | 4 | F | 20160830 | 20090401 | 20160830 | EXP | IN-BRISTOL-MYERS SQUIBB COMPANY-14566186 | BRISTOL MYERS SQUIBB | 27.00 | YR | F | Y | 0.00000 | 20160830 | OT | IN | IN |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 69574934 | 6957493 | 1 | PS | WARFARIN SODIUM. | WARFARIN SODIUM | 1 | Unknown | UNK | U | 9218 | |||||||||
| 69574934 | 6957493 | 2 | SS | HEPARIN | HEPARIN SODIUM | 1 | Unknown | UNK | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 69574934 | 6957493 | 1 | Mitral valve replacement |
| 69574934 | 6957493 | 2 | Mitral valve replacement |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 69574934 | 6957493 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 69574934 | 6957493 | Abdominal pain | |
| 69574934 | 6957493 | Abortion induced | |
| 69574934 | 6957493 | Maternal exposure during pregnancy |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |