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
119822823 11982282 3 F 20160908 20160201 20160908 PER US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-006524 BRISTOL MYERS SQUIBB 58.00 YR F Y 0.00000 20160908 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
119822823 11982282 1 PS SPRYCEL DASATINIB 1 Oral 50 MG, BID U 21986 50 MG FILM-COATED TABLET BID
119822823 11982282 2 C LEVOTHYROXINE SODIUM. LEVOTHYROXINE SODIUM 1 Unknown UNK U 0
119822823 11982282 3 C SUMATRIPTAN. SUMATRIPTAN 1 Unknown UNK U 0
119822823 11982282 4 C AMITRIPTYLINE HCL AMITRIPTYLINE 1 Unknown UNK U 0
119822823 11982282 5 C PROPRANOLOL HCL PROPRANOLOL HYDROCHLORIDE 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119822823 11982282 1 Chronic myeloid leukaemia
119822823 11982282 2 Product used for unknown indication
119822823 11982282 3 Product used for unknown indication
119822823 11982282 4 Product used for unknown indication
119822823 11982282 5 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
119822823 11982282 Fatigue
119822823 11982282 Migraine
119822823 11982282 Off label use
119822823 11982282 White blood cell count decreased

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

no results found

Therapies reported

no results found