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
126867611 12686761 1 I 20160715 20160822 20160825 20160825 EXP GB-BAYER-2016-164209 BAYER 0.00 F Y 0.00000 20160825 OT GB GB

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
126867611 12686761 1 PS ACETYLSALICYLIC ACID (} 100 mg) ASPIRIN 1 Unknown 300 MG, UNK 21317 300 MG TABLET
126867611 12686761 2 SS APIXABAN APIXABAN 1 Unknown UNK 0
126867611 12686761 3 SS APIXABAN APIXABAN 1 0
126867611 12686761 4 SS TRIMETHOPRIM. TRIMETHOPRIM 1 Unknown UNK 0
126867611 12686761 5 SS WARFARIN SODIUM. WARFARIN SODIUM 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126867611 12686761 1 Product used for unknown indication
126867611 12686761 2 Cerebrovascular accident prophylaxis
126867611 12686761 3 Atrial fibrillation
126867611 12686761 4 Product used for unknown indication
126867611 12686761 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126867611 12686761 OT
126867611 12686761 LT
126867611 12686761 HO
126867611 12686761 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
126867611 12686761 Cerebrovascular accident

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
126867611 12686761 2 20160713 0
126867611 12686761 4 20160714 0
126867611 12686761 5 2014 0