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
126255121 12625512 1 I 20140819 20150511 20160805 20160805 EXP JP-VIIV HEALTHCARE LIMITED-JP2015JPN062823 VIIV 0.00 M Y 0.00000 20160805 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
126255121 12625512 1 PS Dolutegravir DOLUTEGRAVIR 1 Oral 50 MG, UNK 204790 50 MG FILM-COATED TABLET
126255121 12625512 2 SS TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Oral 1 DF, UNK 0 1 DF TABLET
126255121 12625512 3 C LYRICA PREGABALIN 1 25 MG, BID 0 25 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126255121 12625512 1 HIV infection
126255121 12625512 2 HIV infection
126255121 12625512 3 Sensory disturbance

Outcome of event

Event ID CASEID OUTC COD
126255121 12625512 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126255121 12625512 Renal impairment
126255121 12625512 Seasonal allergy

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
126255121 12625512 1 20140806 0
126255121 12625512 2 20140806 0
126255121 12625512 3 20140806 20140812 0