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
125813132 12581313 2 F 20160727 20160721 20160803 EXP US-GILEAD-2016-0223619 GILEAD 0.00 M Y 0.00000 20160803 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
125813132 12581313 1 PS TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Unknown UNK 21752 TABLET
125813132 12581313 2 C DOLUTEGRAVIR DOLUTEGRAVIR 1 Unknown UNK 0
125813132 12581313 3 C COBICISTAT W/DARUNAVIR COBICISTATDARUNAVIR ETHANOLATE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125813132 12581313 1 Prophylaxis against HIV infection
125813132 12581313 2 HIV infection
125813132 12581313 3 HIV infection

Outcome of event

Event ID CASEID OUTC COD
125813132 12581313 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125813132 12581313 Drug ineffective
125813132 12581313 Treatment failure
125813132 12581313 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
125813132 12581313 1 20160101 0