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
124018169 12401816 9 F 20160718 20160525 20160809 PER US-PFIZER INC-2016250515 PFIZER 75.00 YR F Y 0.00000 20160809 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
124018169 12401816 1 PS TIKOSYN DOFETILIDE 1 250 UG, 2X/DAY 20931 250 UG CAPSULE, HARD BID
124018169 12401816 2 I TIKOSYN DOFETILIDE 1 20931 CAPSULE, HARD
124018169 12401816 3 I ELIQUIS APIXABAN 1 2.5 MG, 2X/DAY 0 2.5 MG FILM-COATED TABLET BID
124018169 12401816 4 I ELIQUIS APIXABAN 1 0 FILM-COATED TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124018169 12401816 1 Cardiac disorder
124018169 12401816 2 Atrial fibrillation
124018169 12401816 3 Anticoagulant therapy
124018169 12401816 4 Atrial fibrillation

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124018169 12401816 Back pain
124018169 12401816 Condition aggravated
124018169 12401816 Drug interaction
124018169 12401816 Insomnia

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
124018169 12401816 1 201510 0
124018169 12401816 3 201510 0