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
125643651 12564365 1 I 20160706 20160718 20160718 PER US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-056096 BRISTOL MYERS SQUIBB 0.00 M Y 95.24000 KG 20160718 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
125643651 12564365 1 PS SPRYCEL DASATINIB 1 Unknown UNK U 21986

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125643651 12564365 1 Chronic myeloid leukaemia

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125643651 12564365 Chest discomfort
125643651 12564365 Gastric disorder
125643651 12564365 Headache
125643651 12564365 Muscle spasms
125643651 12564365 Pain
125643651 12564365 Vision blurred
125643651 12564365 Visual acuity reduced

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
125643651 12564365 1 20160630 20160705 0