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
98862805 9886280 5 F 20131218 20160901 20140210 20160906 EXP PHHY2013CA063717 NOVARTIS 53.85 YR M Y 0.00000 20160906 MD CA CA

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
98862805 9886280 1 PS GLEEVEC IMATINIB MESYLATE 1 Oral 400 MG, QD 21588 400 MG QD
98862805 9886280 2 SS GLEEVEC IMATINIB MESYLATE 1 Oral 600 MG, QD 21588 600 MG QD
98862805 9886280 3 C IMODIUM LOPERAMIDE HYDROCHLORIDE 1 Unknown Y 0
98862805 9886280 4 C ATIVAN LORAZEPAM 1 Unknown UNK, PRN U 0
98862805 9886280 5 C XARELTO RIVAROXABAN 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
98862805 9886280 1 Chronic myeloid leukaemia
98862805 9886280 3 Product used for unknown indication
98862805 9886280 4 Product used for unknown indication
98862805 9886280 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
98862805 9886280 OT
98862805 9886280 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
98862805 9886280 Atrial fibrillation
98862805 9886280 Cardiac failure congestive
98862805 9886280 Diarrhoea
98862805 9886280 Gastrooesophageal reflux disease
98862805 9886280 Insomnia
98862805 9886280 Musculoskeletal stiffness
98862805 9886280 Pain
98862805 9886280 Palpitations
98862805 9886280 Polymyalgia rheumatica
98862805 9886280 Renal failure
98862805 9886280 Therapeutic response 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
98862805 9886280 1 20051001 0