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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127597321 | 12759732 | 1 | I | 20160912 | 20160919 | 20160919 | EXP | DE-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-075066 | BRISTOL MYERS SQUIBB | 75.00 | YR | M | Y | 0.00000 | 20160919 | CN | DE | DE |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127597321 | 12759732 | 1 | PS | ELIQUIS | APIXABAN | 1 | Oral | 5 MG, BID | U | U | 202155 | 5 | MG | FILM-COATED TABLET | BID | ||||
| 127597321 | 12759732 | 2 | SS | FLECAINIDE ACETATE. | FLECAINIDE ACETATE | 1 | Unknown | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127597321 | 12759732 | 1 | Cerebrovascular accident prophylaxis |
| 127597321 | 12759732 | 2 | Arrhythmia |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127597321 | 12759732 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127597321 | 12759732 | Atrial fibrillation | |
| 127597321 | 12759732 | Condition aggravated | |
| 127597321 | 12759732 | Drug intolerance | |
| 127597321 | 12759732 | Epistaxis | |
| 127597321 | 12759732 | Flatulence | |
| 127597321 | 12759732 | Injury | |
| 127597321 | 12759732 | Pain in extremity |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |