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
951221010 9512210 10 F 201408 20160906 20130910 20160913 EXP PHHY2012CA123288 NOVARTIS 72.02 YR M Y 0.00000 20160913 CN COUNTRY NOT SPECIFIED 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
951221010 9512210 1 PS TASIGNA NILOTINIB 1 Oral 400 MG, BID 22068 400 MG CAPSULE BID
951221010 9512210 2 SS COLCHICINE. COLCHICINE 1 Unknown UNK Y 0
951221010 9512210 3 C TYLENOL ACETAMINOPHEN 1 Unknown UNK, PRN U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
951221010 9512210 1 Chronic myeloid leukaemia
951221010 9512210 2 Product used for unknown indication
951221010 9512210 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
951221010 9512210 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
951221010 9512210 Abdominal pain upper
951221010 9512210 Blood pressure fluctuation
951221010 9512210 Cough
951221010 9512210 Diarrhoea
951221010 9512210 Dizziness
951221010 9512210 Eye pain
951221010 9512210 Fatigue
951221010 9512210 Fear
951221010 9512210 Gout
951221010 9512210 Headache
951221010 9512210 Hiccups
951221010 9512210 Malaise
951221010 9512210 Nasopharyngitis
951221010 9512210 Ocular hyperaemia
951221010 9512210 Pain in extremity
951221010 9512210 Peripheral swelling
951221010 9512210 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
951221010 9512210 1 201006 0
951221010 9512210 2 20120902 0