The Safety Rates Drug Report

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Drug     Injury     Quarter    

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
126108293 12610829 3 F 201601 20160822 20160801 20160902 PER US-PFIZER INC-2016327190 PFIZER 79.00 YR F Y 0.00000 20160902 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
126108293 12610829 1 PS TIKOSYN DOFETILIDE 1 250 UG, UNK N 20931 250 UG CAPSULE, HARD
126108293 12610829 2 SS TIKOSYN DOFETILIDE 1 0.25 MG, UNK N 20931 .25 MG CAPSULE, HARD
126108293 12610829 3 C ELIQUIS APIXABAN 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126108293 12610829 1 Supraventricular tachycardia
126108293 12610829 2 Atrial fibrillation
126108293 12610829 3 Supraventricular tachycardia

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126108293 12610829 Dizziness
126108293 12610829 Visual impairment

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
126108293 12610829 1 201511 0
126108293 12610829 2 20151110 0
126108293 12610829 3 20151110 0