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
119699103 11969910 3 F 20151130 20160913 20160128 20160914 EXP UG-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-004607 BRISTOL MYERS SQUIBB 27.46 YR F Y 61.50000 KG 20160914 OT UG 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
119699103 11969910 1 SS ETOPOSIDE. ETOPOSIDE 1 Oral 50 MG, QD 9000 MG 0 50 MG QD
119699103 11969910 2 SS ETOPOSIDE. ETOPOSIDE 1 Oral 100 UNK, UNK 9000 MG 0 100 MG QD
119699103 11969910 3 PS EFAVIRENZ, EMTRICITABINE, AND TENOFOVIR DISOPROXIL FUMARATE EFAVIRENZEMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Oral 1100 MG, UNK 21937 1100 MG FILM-COATED TABLET QD
119699103 11969910 4 C COTRIMOXAZOLE SULFAMETHOXAZOLETRIMETHOPRIM 1 Oral UNK, QID 0 QID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119699103 11969910 1 Acquired immunodeficiency syndrome
119699103 11969910 3 Acquired immunodeficiency syndrome
119699103 11969910 4 Prophylaxis

Outcome of event

Event ID CASEID OUTC COD
119699103 11969910 HO
119699103 11969910 OT
119699103 11969910 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
119699103 11969910 Acute respiratory distress syndrome
119699103 11969910 Pyrexia

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
119699103 11969910 1 20150408 20150501 0
119699103 11969910 2 20150506 20150722 0
119699103 11969910 3 20150407 20151129 0
119699103 11969910 4 20151129 0