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
125629841 12562984 1 I 20101202 20160712 20160715 20160715 EXP US-GILEAD-2016-0223582 GILEAD 49.00 YR A M Y 94.33000 KG 20160715 OT 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
125629841 12562984 1 PS TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Unknown 1 DF, QD 21752 1 DF TABLET QD
125629841 12562984 2 C ISENTRESS RALTEGRAVIR POTASSIUM 1 400 MG, BID 0 400 MG BID
125629841 12562984 3 C NEURONTIN GABAPENTIN 1 0
125629841 12562984 4 C LYRICA PREGABALIN 1 0
125629841 12562984 5 C COUMADIN WARFARIN SODIUM 1 0
125629841 12562984 6 C VALTREX VALACYCLOVIR HYDROCHLORIDE 1 0
125629841 12562984 7 C LANTUS INSULIN GLARGINE 1 0
125629841 12562984 8 C FAMVIR FAMCICLOVIR 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125629841 12562984 1 HIV infection

Outcome of event

Event ID CASEID OUTC COD
125629841 12562984 HO
125629841 12562984 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125629841 12562984 Atrial fibrillation
125629841 12562984 Chest pain
125629841 12562984 Herpes zoster

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
125629841 12562984 1 20100223 0
125629841 12562984 2 20100223 0