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
120783864 12078386 4 F 20160711 20160216 20160720 PER US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-011128 BRISTOL MYERS SQUIBB 0.00 F 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
120783864 12078386 1 PS SPRYCEL DASATINIB 1 Oral 1 UNK, UNK U U 21986 100 MG QD
120783864 12078386 2 SS SPRYCEL DASATINIB 1 Oral 100 MG, UNK U U 21986 100 MG QD
120783864 12078386 3 C FOLIC ACID. FOLIC ACID 1 Unknown U 0
120783864 12078386 4 C IRON IRON 1 Unknown U 0
120783864 12078386 5 C VITAMIN D /00107901/ ERGOCALCIFEROL 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
120783864 12078386 1 Chronic myeloid leukaemia
120783864 12078386 3 Product used for unknown indication
120783864 12078386 4 Product used for unknown indication
120783864 12078386 5 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
120783864 12078386 Abdominal discomfort
120783864 12078386 Alopecia
120783864 12078386 Appetite disorder
120783864 12078386 Decreased appetite
120783864 12078386 Dyspnoea
120783864 12078386 Fatigue
120783864 12078386 Myalgia
120783864 12078386 Nausea
120783864 12078386 Weight decreased

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
120783864 12078386 1 20151223 0
120783864 12078386 2 20151223 0