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
125729502 12572950 2 F 201602 20160829 20160720 20160909 EXP US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-056375 BRISTOL MYERS SQUIBB 85.18 YR M Y 0.00000 20160909 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
125729502 12572950 1 PS COUMADIN WARFARIN SODIUM 1 Unknown U 9218
125729502 12572950 2 SS XTANDI ENZALUTAMIDE 1 Unknown 160 MG, QD U 1507024 PCC/151682501152665OPC 0 160 MG CAPSULE QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125729502 12572950 1 Product used for unknown indication
125729502 12572950 2 Prostate cancer

Outcome of event

Event ID CASEID OUTC COD
125729502 12572950 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125729502 12572950 Arthralgia
125729502 12572950 Arthritis
125729502 12572950 Back pain
125729502 12572950 Coordination abnormal
125729502 12572950 Dry eye
125729502 12572950 Eye disorder
125729502 12572950 Fall
125729502 12572950 Fatigue
125729502 12572950 Heart rate irregular
125729502 12572950 Hip deformity
125729502 12572950 International normalised ratio decreased
125729502 12572950 International normalised ratio fluctuation
125729502 12572950 Micturition urgency
125729502 12572950 Poor quality sleep
125729502 12572950 Vision blurred

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
125729502 12572950 2 20151022 0