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
126652321 12665232 1 I 20141231 20160812 20160818 20160818 EXP MY-SA-2016SA148997 AVENTIS 79.00 YR E M Y 0.00000 20160818 CN MY MY

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
126652321 12665232 1 PS PLAVIX CLOPIDOGREL BISULFATE 1 Oral U U 20839 TABLET
126652321 12665232 2 SS COAPROVEL HYDROCHLOROTHIAZIDEIRBESARTAN 1 Oral U U 20758
126652321 12665232 3 SS ELIQUIS APIXABAN 1 Oral U U 0 5 MG QD
126652321 12665232 4 SS CLOPIDOGREL CLOPIDOGREL BISULFATE 1 Unknown U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126652321 12665232 2 Cerebrovascular accident prophylaxis
126652321 12665232 3 Cerebrovascular accident prophylaxis
126652321 12665232 4 Cerebrovascular accident prophylaxis

Outcome of event

Event ID CASEID OUTC COD
126652321 12665232 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
126652321 12665232 Haemorrhage intracranial

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
126652321 12665232 1 2014 0
126652321 12665232 2 2014 0
126652321 12665232 3 2014 0
126652321 12665232 4 2014 0