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
123269472 12326947 2 F 20160422 20160708 20160503 20160720 PER US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-032330 BRISTOL MYERS SQUIBB 27.87 YR M Y 0.00000 20160720 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
123269472 12326947 1 PS SPRYCEL DASATINIB 1 Oral 100 MG, QD U 21986 100 MG FILM-COATED TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123269472 12326947 1 Chronic myeloid leukaemia

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
123269472 12326947 Chest discomfort
123269472 12326947 Chest pain
123269472 12326947 Dyspnoea
123269472 12326947 Headache
123269472 12326947 Hot flush
123269472 12326947 Muscular weakness
123269472 12326947 Nausea
123269472 12326947 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
123269472 12326947 1 20160405 0