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
127077352 12707735 2 F 20160921 20160924 20160901 20160930 EXP US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-071603 BRISTOL MYERS SQUIBB 84.24 YR F Y 0.00000 20160930 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
127077352 12707735 1 PS SPRYCEL DASATINIB 1 Unknown 100 MG, QD U 21986 100 MG FILM-COATED TABLET QD
127077352 12707735 2 SS SPRYCEL DASATINIB 1 Unknown 100 MG, QD U 21986 100 MG FILM-COATED TABLET QD
127077352 12707735 3 SS SPRYCEL DASATINIB 1 Unknown 70 MG, QD U 21986 70 MG FILM-COATED TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127077352 12707735 1 Acute myeloid leukaemia

Outcome of event

Event ID CASEID OUTC COD
127077352 12707735 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127077352 12707735 Diarrhoea
127077352 12707735 Malaise
127077352 12707735 Product use issue
127077352 12707735 Vomiting

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
127077352 12707735 1 20160704 0
127077352 12707735 2 20160815 0
127077352 12707735 3 20160920 0