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
125882072 12588207 2 F 19970114 20160822 20160725 20160901 EXP CA-GILEAD-2016-0224316 GILEAD 69.00 YR E M Y 0.00000 20160901 MD CA CA

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
125882072 12588207 1 PS EMTRICITABINE EMTRICITABINE 1 Unknown U 21500 CAPSULE
125882072 12588207 2 SS TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Unknown U 0 TABLET
125882072 12588207 3 SS LAMIVUDINE. LAMIVUDINE 1 Unknown UNK U 0
125882072 12588207 4 SS LAMIVUDINE. LAMIVUDINE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125882072 12588207 1 HIV infection
125882072 12588207 2 HIV infection
125882072 12588207 3 HIV infection
125882072 12588207 4 Hepatitis B

Outcome of event

Event ID CASEID OUTC COD
125882072 12588207 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125882072 12588207 Viral mutation identified

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
125882072 12588207 3 1995 0