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
123183262 12318326 2 F 20160919 20160429 20160926 EXP US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-032290 BRISTOL MYERS SQUIBB 0.00 M Y 0.00000 20160926 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
123183262 12318326 1 PS SPRYCEL DASATINIB 1 Oral 100 MG, QD 21986 100 MG QD
123183262 12318326 2 SS SPRYCEL DASATINIB 1 Oral 70 MG, QD 21986 70 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123183262 12318326 1 Chronic myeloid leukaemia

Outcome of event

Event ID CASEID OUTC COD
123183262 12318326 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123183262 12318326 Dyspnoea
123183262 12318326 Erythema
123183262 12318326 Eye swelling
123183262 12318326 Flushing
123183262 12318326 Hypertension
123183262 12318326 Pericardial effusion
123183262 12318326 Pleural effusion

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
123183262 12318326 1 20150929 0
123183262 12318326 2 201507 0