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
123415164 12341516 4 F 20160428 20160819 20160506 20160824 EXP PHHY2016CR061990 NOVARTIS 57.00 YR F Y 0.00000 20160824 CN COUNTRY NOT SPECIFIED CR

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
123415164 12341516 1 PS TASIGNA NILOTINIB 1 Unknown 2 DF (IN THE MORNING AT 9.30 AND AT NIGHT AT 21.30 TO 22.00 HOURS), Q12H U 22068 2 DF CAPSULE Q12H
123415164 12341516 2 C INSULIN CRYSTALINE 2 Unknown U 0
123415164 12341516 3 C INSULIN INSULIN NOS 1 Unknown U 0
123415164 12341516 4 C IRBESARTAN. IRBESARTAN 1 Unknown U 0
123415164 12341516 5 C VITAMIN D CHOLECALCIFEROL 1 Unknown U 0
123415164 12341516 6 C ALENDRONATE ALENDRONATE SODIUM 1 Unknown U 0
123415164 12341516 7 C ALLEGRA FEXOFENADINE HYDROCHLORIDE 1 Unknown U 0
123415164 12341516 8 C LEVOTHYROXINE. LEVOTHYROXINE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123415164 12341516 1 Chronic myeloid leukaemia
123415164 12341516 2 Diabetes mellitus
123415164 12341516 3 Diabetes mellitus
123415164 12341516 4 Hypertension
123415164 12341516 5 Osteoporosis
123415164 12341516 6 Osteoporosis
123415164 12341516 7 Psoriasis
123415164 12341516 8 Thyroid disorder

Outcome of event

Event ID CASEID OUTC COD
123415164 12341516 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123415164 12341516 Chest pain
123415164 12341516 Dysarthria
123415164 12341516 Ear pain
123415164 12341516 Facial pain
123415164 12341516 Facial paralysis
123415164 12341516 Gait disturbance
123415164 12341516 Hypoaesthesia oral
123415164 12341516 Movement disorder
123415164 12341516 Muscular weakness
123415164 12341516 Nausea
123415164 12341516 Neck pain
123415164 12341516 Osteoporosis
123415164 12341516 Pain in extremity
123415164 12341516 Paraesthesia oral
123415164 12341516 Vision blurred
123415164 12341516 Visual impairment
123415164 12341516 Vomiting

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
123415164 12341516 1 2014 0