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
116324713 11632471 3 F 201409 20160905 20151015 20160908 EXP JP-VIIV HEALTHCARE LIMITED-JP2015JPN144183 VIIV 0.00 A M Y 0.00000 20160908 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
116324713 11632471 1 PS Dolutegravir DOLUTEGRAVIR 1 Oral 50 MG, UNK 204790 50 MG FILM-COATED TABLET
116324713 11632471 2 SS TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Oral 1 DF, UNK 0 1 DF
116324713 11632471 3 C Samitrel ATOVAQUONE 1 Oral 750 MG, BID 96000 MG 0 750 MG BID
116324713 11632471 4 C Samitrel ATOVAQUONE 1 1500 MG, QD 96000 MG 0 1500 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
116324713 11632471 1 HIV infection
116324713 11632471 2 HIV infection
116324713 11632471 3 Pneumocystis jirovecii pneumonia
116324713 11632471 4 Antifungal prophylaxis

Outcome of event

Event ID CASEID OUTC COD
116324713 11632471 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
116324713 11632471 Rash
116324713 11632471 Renal impairment

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
116324713 11632471 1 20140804 0
116324713 11632471 2 20140804 0
116324713 11632471 3 20140630 20140709 0
116324713 11632471 4 20140710 20150107 0