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
113142475 11314247 5 F 201408 20160901 20150727 20160907 EXP JP-GLAXOSMITHKLINE-JP2015JPN104027 GLAXOSMITHKLINE 72.00 YR M Y 0.00000 20160907 CN JP JP

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
113142475 11314247 1 SS Dolutegravir DOLUTEGRAVIR 1 Oral 50 MG, UNK Y 0 50 MG FILM-COATED TABLET
113142475 11314247 2 PS EPZICOM ABACAVIR SULFATELAMIVUDINE 1 Oral 1 DF, UNK Y 21652 1 DF TABLET
113142475 11314247 3 SS ISENTRESS RALTEGRAVIR POTASSIUM 1 Oral 800 MG, UNK 0 800 MG TABLET
113142475 11314247 4 C TRIUMEQ ABACAVIR SULFATEDOLUTEGRAVIR SODIUMLAMIVUDINE 1 Oral 1 DF, UNK 0 1 DF FILM-COATED TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
113142475 11314247 1 HIV infection
113142475 11314247 2 HIV infection
113142475 11314247 3 HIV infection
113142475 11314247 4 HIV infection

Outcome of event

Event ID CASEID OUTC COD
113142475 11314247 HO
113142475 11314247 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
113142475 11314247 Hyperuricaemia
113142475 11314247 Thymoma

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
113142475 11314247 1 20140717 20150528 0
113142475 11314247 2 20100611 20150528 0
113142475 11314247 3 20100611 20140716 0
113142475 11314247 4 20150529 201511 0