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
123902064 12390206 4 F 20160704 20160520 20160711 EXP CL-GILEAD-2016-0214766 GILEAD 0.00 A Y 0.00000 20160711 OT CL CL

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
123902064 12390206 1 PS TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Oral UNK, QD Y 21752 TABLET QD
123902064 12390206 2 C DIDANOSINA 2 Unknown 400 MG, QD Y 0 400 MG QD
123902064 12390206 3 C ATAZANAVIR ATAZANAVIR 1 UNK 0
123902064 12390206 4 C LOPINAVIR LOPINAVIR 1 UNK Y 0
123902064 12390206 5 C RITONAVIR. RITONAVIR 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123902064 12390206 1 HIV infection
123902064 12390206 2 HIV infection
123902064 12390206 3 HIV infection
123902064 12390206 4 HIV infection
123902064 12390206 5 HIV infection

Outcome of event

Event ID CASEID OUTC COD
123902064 12390206 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123902064 12390206 Drug interaction
123902064 12390206 Dysaesthesia
123902064 12390206 Neuropathy peripheral

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
123902064 12390206 1 20160510 20160510 0
123902064 12390206 2 2007 20160509 0