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
122474792 12247479 2 F 201603 20160711 20160407 20160712 PER US-GILEAD-2016-0207404 GILEAD 70.00 YR E M Y 0.00000 20160712 MD 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
122474792 12247479 1 PS TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Unknown UNK U 21752 TABLET
122474792 12247479 2 SS TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 U 21752 TABLET
122474792 12247479 3 SS ATRIPLA EFAVIRENZEMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Unknown UNK U 0 TABLET
122474792 12247479 4 SS ATRIPLA EFAVIRENZEMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 U 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122474792 12247479 1 Chronic hepatitis B
122474792 12247479 2 HIV infection
122474792 12247479 3 Chronic hepatitis B
122474792 12247479 4 HIV infection

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
122474792 12247479 Blood calcium decreased
122474792 12247479 Creatinine renal clearance increased
122474792 12247479 Nephropathy
122474792 12247479 Osteopenia

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
122474792 12247479 1 2002 0
122474792 12247479 3 2002 0