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
127227471 12722747 1 I 20160902 20160907 20160907 PER US-GILEAD-2016-0232006 GILEAD 0.00 A M Y 0.00000 20160907 CN 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
127227471 12722747 1 PS STRIBILD COBICISTATELVITEGRAVIREMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Unknown UNK 203100 TABLET
127227471 12722747 2 SS PREZISTA DARUNAVIR ETHANOLATE 1 Unknown UNK 0
127227471 12722747 3 SS PLAQUENIL /00072602/ HYDROXYCHLOROQUINE DIPHOSPHATE 1 Unknown 400 MG, BID U 0 400 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127227471 12722747 1 HIV infection
127227471 12722747 2 HIV infection
127227471 12722747 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127227471 12722747 Drug interaction
127227471 12722747 T-lymphocyte count decreased

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
127227471 12722747 1 2013 0
127227471 12722747 2 2013 0