The Safety Rates Drug Report

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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
125629741 12562974 1 I 201604 20160627 20160715 20160715 EXP US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-057073 BRISTOL MYERS SQUIBB 82.82 YR F Y 45.36000 KG 20160715 PH 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
125629741 12562974 1 PS ELIQUIS APIXABAN 1 Oral 2.5 MG, Q12H 202155 2.5 MG BID
125629741 12562974 2 SS SOTALOL HYDROCHLORIDE. SOTALOL HYDROCHLORIDE 1 Unknown 80 MG, BID Y 0 80 MG BID
125629741 12562974 3 SS TIKOSYN DOFETILIDE 1 Oral 0.25 ?G, BID 0 .25 UG BID
125629741 12562974 4 C METOPROLOL. METOPROLOL 1 Oral 50 MG, BID 0 50 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125629741 12562974 1 Cerebrovascular accident prophylaxis
125629741 12562974 2 Atrial fibrillation
125629741 12562974 3 Atrial fibrillation
125629741 12562974 4 Arrhythmia

Outcome of event

Event ID CASEID OUTC COD
125629741 12562974 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125629741 12562974 Atrial fibrillation
125629741 12562974 Headache
125629741 12562974 Nausea

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
125629741 12562974 1 201604 0
125629741 12562974 2 20160413 201606 0
125629741 12562974 3 20160615 0
125629741 12562974 4 2015 0