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
126940741 12694074 1 I 20130502 20160816 20160829 20160829 EXP FR-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-068380 BRISTOL MYERS SQUIBB 79.93 YR M Y 0.00000 20160829 CN FR FR

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
126940741 12694074 1 PS COUMADINE WARFARIN SODIUM 1 Oral Y 9218 TABLET
126940741 12694074 2 SS LOVENOX ENOXAPARIN SODIUM 1 Oral UNK Y 0
126940741 12694074 3 SS KARDEGIC ASPIRIN LYSINE 1 Oral UNK Y 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126940741 12694074 1 Atrial fibrillation
126940741 12694074 2 Product used for unknown indication
126940741 12694074 3 Cerebrovascular accident

Outcome of event

Event ID CASEID OUTC COD
126940741 12694074 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126940741 12694074 Haemoptysis

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
126940741 12694074 2 201304 20130502 0
126940741 12694074 3 20130502 0