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
113063326 11306332 6 F 201408 20160901 20150723 20160907 EXP JP-VIIV HEALTHCARE LIMITED-JP2015JPN104027 VIIV 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
113063326 11306332 1 PS Dolutegravir DOLUTEGRAVIR 1 Oral 50 MG, UNK Y 204790 50 MG FILM-COATED TABLET
113063326 11306332 2 SS EPZICOM ABACAVIR SULFATELAMIVUDINE 1 Oral 1 DF, UNK Y 0 1 DF TABLET
113063326 11306332 3 SS ISENTRESS RALTEGRAVIR POTASSIUM 1 Oral 800 MG, UNK 0 800 MG TABLET
113063326 11306332 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
113063326 11306332 1 HIV infection
113063326 11306332 2 HIV infection
113063326 11306332 3 HIV infection
113063326 11306332 4 HIV infection

Outcome of event

Event ID CASEID OUTC COD
113063326 11306332 HO
113063326 11306332 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
113063326 11306332 Hyperuricaemia
113063326 11306332 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
113063326 11306332 1 20140717 20150528 0
113063326 11306332 2 20100611 20150528 0
113063326 11306332 3 20100611 20140716 0
113063326 11306332 4 20150529 201511 0