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
125541422 12554142 2 F 20160712 20160713 20160715 EXP AT-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-056677 BRISTOL MYERS SQUIBB 0.00 F Y 0.00000 20160715 MD AT AT

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
125541422 12554142 1 PS BARACLUDE ENTECAVIR 1 Unknown U 21797
125541422 12554142 2 SS TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Unknown 0
125541422 12554142 3 SS EMTRIVA EMTRICITABINE 1 Unknown U 0
125541422 12554142 4 SS TIVICAY DOLUTEGRAVIR SODIUM 1 Unknown U 0
125541422 12554142 5 SS PREZISTA DARUNAVIR ETHANOLATE 1 Unknown U 0
125541422 12554142 6 SS NORVIR RITONAVIR 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125541422 12554142 1 Product used for unknown indication
125541422 12554142 2 Product used for unknown indication
125541422 12554142 3 Product used for unknown indication
125541422 12554142 4 Product used for unknown indication
125541422 12554142 5 Product used for unknown indication
125541422 12554142 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125541422 12554142 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125541422 12554142 Blood creatinine increased
125541422 12554142 Liver transplant
125541422 12554142 Renal failure

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found