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
126358281 12635828 1 I 20160805 20160809 20160809 PER US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-064694 BRISTOL MYERS SQUIBB 0.00 M Y 0.00000 20160809 MD 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
126358281 12635828 1 PS SPRYCEL DASATINIB 1 Oral 140 MG, QD U U 21986 140 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126358281 12635828 1 Lymphoma

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126358281 12635828 Abdominal pain
126358281 12635828 Abdominal pain upper
126358281 12635828 Back pain
126358281 12635828 Nausea
126358281 12635828 Pain
126358281 12635828 Retching
126358281 12635828 Vomiting

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found