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
116610943 11661094 3 F 20131025 20160805 20151026 20160812 EXP PHHY2015IT122825 NOVARTIS 43.74 YR M Y 81.00000 KG 20160812 OT IT IT

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
116610943 11661094 1 PS TASIGNA NILOTINIB 1 Oral 600 MG, QD 657000 MG Y 22068 600 MG CAPSULE QD
116610943 11661094 2 C CITALOPRAM CITALOPRAM HYDROBROMIDE 1 Unknown 20 MG, QD 7320 MG Y 0 20 MG QD
116610943 11661094 3 C CITALOPRAM CITALOPRAM HYDROBROMIDE 1 Unknown 10 MG, QD 7320 MG Y 0 10 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
116610943 11661094 1 Chronic myeloid leukaemia
116610943 11661094 2 Depression

Outcome of event

Event ID CASEID OUTC COD
116610943 11661094 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
116610943 11661094 Asthenia
116610943 11661094 Blood bilirubin increased
116610943 11661094 Insomnia
116610943 11661094 Intermittent claudication
116610943 11661094 Periorbital oedema
116610943 11661094 Peripheral arterial occlusive disease
116610943 11661094 Peripheral artery restenosis
116610943 11661094 Transaminases increased
116610943 11661094 Vascular stenosis

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
116610943 11661094 1 20101027 20141107 0
116610943 11661094 2 20121025 20131201 0
116610943 11661094 3 20131202 20140626 0