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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127765501 | 12776550 | 1 | I | 20160915 | 20160923 | 20160923 | EXP | US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-077438 | BRISTOL MYERS SQUIBB | 0.00 | F | Y | 81.65000 | KG | 20160923 | CN | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127765501 | 12776550 | 1 | PS | ELIQUIS | APIXABAN | 1 | Unknown | U | 202155 | ||||||||||
127765501 | 12776550 | 2 | SS | MULTAQ | DRONEDARONE | 1 | Unknown | U | 0 | ||||||||||
127765501 | 12776550 | 3 | SS | LYRICA | PREGABALIN | 1 | Unknown | Y | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127765501 | 12776550 | 1 | Product used for unknown indication |
127765501 | 12776550 | 2 | Product used for unknown indication |
127765501 | 12776550 | 3 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127765501 | 12776550 | OT |
127765501 | 12776550 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127765501 | 12776550 | Atrial fibrillation | |
127765501 | 12776550 | Sensory disturbance |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |