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
127116961 12711696 1 I 20160715 20160822 20160902 20160902 EXP GB-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-122837 RANBAXY 0.00 F Y 0.00000 20160902 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
127116961 12711696 1 SS ASPIRIN. ASPIRIN 1 Unknown 300 MG U 0 300 MG
127116961 12711696 2 PS TRIMETHOPRIM. TRIMETHOPRIM 1 Unknown UNK U U 70495
127116961 12711696 3 SS Warfarin WARFARIN 1 Unknown UNK U 0
127116961 12711696 4 SS ELIQUIS APIXABAN 1 Unknown UNK U U 0
127116961 12711696 5 SS ELIQUIS APIXABAN 1 U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127116961 12711696 1 Product used for unknown indication
127116961 12711696 2 Product used for unknown indication
127116961 12711696 3 Product used for unknown indication
127116961 12711696 4 Cerebrovascular accident prophylaxis
127116961 12711696 5 Atrial fibrillation

Outcome of event

Event ID CASEID OUTC COD
127116961 12711696 HO
127116961 12711696 LT
127116961 12711696 OT
127116961 12711696 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
127116961 12711696 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
127116961 12711696 2 20160714 0
127116961 12711696 4 20160713 0