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
115420863 11542086 3 F 201504 20160903 20150923 20160903 PER US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2015-061486 BRISTOL MYERS SQUIBB 67.70 YR F Y 0.00000 20160903 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
115420863 11542086 1 PS SPRYCEL DASATINIB 1 Oral 70 MG, QD Y U 21986 70 MG QD
115420863 11542086 2 SS SPRYCEL DASATINIB 1 Y U 21986
115420863 11542086 3 SS CIPRO CIPROFLOXACIN HYDROCHLORIDE 1 Unknown 500 MG, BID U 0 500 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
115420863 11542086 1 Chronic myeloid leukaemia
115420863 11542086 2 Chronic myeloid leukaemia
115420863 11542086 3 Sinusitis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
115420863 11542086 Blister
115420863 11542086 Dermatitis acneiform
115420863 11542086 Diarrhoea
115420863 11542086 Erythema
115420863 11542086 Prescribed underdose
115420863 11542086 Rash
115420863 11542086 Stomatitis

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
115420863 11542086 1 20150226 0
115420863 11542086 3 20150324 0