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
119044833 11904483 3 F 20160906 20160111 20160907 PER US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-000918 BRISTOL MYERS SQUIBB 0.00 F Y 0.00000 20160907 OT 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
119044833 11904483 1 PS SPRYCEL DASATINIB 1 Oral 100MG U U 21986 100 MG QD
119044833 11904483 2 SS SPRYCEL DASATINIB 1 U U 21986
119044833 11904483 3 C ZESTRIL LISINOPRIL 1 Unknown U 0
119044833 11904483 4 C MULTIVITAMIN /00097801/ VITAMINS 1 Unknown U 0
119044833 11904483 5 C AMLODIPINE AMLODIPINE BESYLATE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119044833 11904483 1 Chronic myeloid leukaemia
119044833 11904483 2 Chronic lymphocytic leukaemia
119044833 11904483 3 Product used for unknown indication
119044833 11904483 4 Product used for unknown indication
119044833 11904483 5 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
119044833 11904483 Abdominal discomfort
119044833 11904483 Drug dose omission
119044833 11904483 Nausea
119044833 11904483 Product use issue

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
119044833 11904483 1 20140814 0