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
126080741 12608074 1 I 2010 20160707 20160729 20160729 EXP CA-GILEAD-2016-0223173 GILEAD 0.00 M Y 58.70000 KG 20160729 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
126080741 12608074 1 PS TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Unknown UNK U 21752 TABLET
126080741 12608074 2 C NEVIRAPINE. NEVIRAPINE 1 Unknown UNK 0
126080741 12608074 3 C GABAPENTIN. GABAPENTIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126080741 12608074 1 HIV infection
126080741 12608074 2 HIV infection
126080741 12608074 3 Convulsion prophylaxis

Outcome of event

Event ID CASEID OUTC COD
126080741 12608074 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126080741 12608074 Bone density decreased
126080741 12608074 Fanconi syndrome acquired
126080741 12608074 Glycosuria
126080741 12608074 Hypophosphataemia
126080741 12608074 Nephropathy toxic
126080741 12608074 Urine phosphorus increased

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
126080741 12608074 1 2005 0