The Safety Rates Drug Report

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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
125289072 12528907 2 F 20160421 20160623 20160705 20160705 EXP UG-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-034189 BRISTOL MYERS SQUIBB 36.30 YR M Y 60.00000 KG 20160705 CN US UG

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
125289072 12528907 1 SS ETOPOSIDE. ETOPOSIDE 1 Oral 200 MG, BID U 0 200 MG CAPSULE BID
125289072 12528907 2 PS EFAVIRENZ, EMTRICITABINE, AND TENOFOVIR DISOPROXIL FUMARATE EFAVIRENZEMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Oral 1100 MG, QD 21937 1100 MG FILM-COATED TABLET QD
125289072 12528907 3 C COTRIMOXAZOLE SULFAMETHOXAZOLETRIMETHOPRIM 1 Oral UNK, QD U 0 QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125289072 12528907 1 Acquired immunodeficiency syndrome
125289072 12528907 2 Acquired immunodeficiency syndrome
125289072 12528907 3 Prophylaxis

Outcome of event

Event ID CASEID OUTC COD
125289072 12528907 OT
125289072 12528907 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125289072 12528907 Encephalitis
125289072 12528907 Neutropenia

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
125289072 12528907 1 20151021 0
125289072 12528907 2 20151021 0
125289072 12528907 3 20160420 0