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
114609393 11460939 3 F 20150411 20160621 20150904 20160704 EXP TH-BRISTOL-MYERS SQUIBB COMPANY-BMS-2015-057252 BRISTOL MYERS SQUIBB 30.00 YR F Y 0.00000 20160704 OT TH TH

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
114609393 11460939 1 PS EFAVIRENZ EFAVIRENZ 1 Oral 600 MG, QD 20972 600 MG QD
114609393 11460939 2 SS TENOFOVIR DISOPROXIL FUMARATE. TENOFOVIR DISOPROXIL FUMARATE 1 Oral 300 MG, QD 0 300 MG QD
114609393 11460939 3 SS LAMIVUDINE. LAMIVUDINE 1 Oral 300 MG, QD 0 300 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
114609393 11460939 1 HIV infection
114609393 11460939 2 HIV infection
114609393 11460939 3 HIV infection

Outcome of event

Event ID CASEID OUTC COD
114609393 11460939 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
114609393 11460939 Abortion spontaneous
114609393 11460939 Maternal exposure during pregnancy
114609393 11460939 Off label use

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
114609393 11460939 1 20140604 0
114609393 11460939 2 20140604 0
114609393 11460939 3 20140604 0