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
127359921 12735992 1 I 20130109 20160804 20160913 20160913 EXP ZA-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-069863 BRISTOL MYERS SQUIBB 29.00 YR F Y 0.00000 20160913 CN FR ZA

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
127359921 12735992 1 SS EFAVIRENZ EFAVIRENZ 1 Unknown 600 MG, QD 158400 MG Y 0 600 MG CAPSULE QD
127359921 12735992 2 PS EFAVIRENZ, EMTRICITABINE, AND TENOFOVIR DISOPROXIL FUMARATE EFAVIRENZEMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Unknown 1 DF, QD U 21937 1 DF FILM-COATED TABLET QD
127359921 12735992 3 SS TENOFOVIR TENOFOVIR 1 Unknown 300 MG, QD 106800 MG Y 0 300 MG QD
127359921 12735992 4 SS LAMIVUDINE. LAMIVUDINE 1 Unknown 300 MG, QD 79200 MG Y 0 300 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127359921 12735992 1 HIV infection
127359921 12735992 2 HIV infection
127359921 12735992 3 HIV infection
127359921 12735992 4 HIV infection

Outcome of event

Event ID CASEID OUTC COD
127359921 12735992 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127359921 12735992 Caesarean section
127359921 12735992 Maternal exposure during pregnancy
127359921 12735992 Normal newborn

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
127359921 12735992 1 20110917 20120606 0
127359921 12735992 2 20120606 0
127359921 12735992 3 20110617 20120606 0
127359921 12735992 4 20110917 20120606 0