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
127196122 12719612 2 F 20160913 20160907 20160920 EXP PHHY2015CR106971 NOVARTIS 57.00 YR M Y 86.00000 KG 20160920 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
127196122 12719612 1 PS TASIGNA NILOTINIB 1 Unknown 800 MG, QD (10 AM AND AT 3 PM) 22068 800 MG CAPSULE QD
127196122 12719612 2 SS TASIGNA NILOTINIB 1 Unknown 800 MG, QD (2 AT 10 AM AND 2 AT 10 PM) 22068 800 MG CAPSULE QD
127196122 12719612 3 SS TASIGNA NILOTINIB 1 Oral 400 MG, BID 22068 400 MG CAPSULE BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127196122 12719612 1 Chronic myeloid leukaemia

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127196122 12719612 Abdominal discomfort
127196122 12719612 Abdominal pain
127196122 12719612 Abdominal pain upper
127196122 12719612 Blister
127196122 12719612 Constipation
127196122 12719612 Eye irritation
127196122 12719612 Fatigue
127196122 12719612 Gastritis
127196122 12719612 Hyperchlorhydria
127196122 12719612 Incorrect drug administration duration
127196122 12719612 Nasopharyngitis
127196122 12719612 Rash
127196122 12719612 Visual impairment

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

no results found

Therapies reported

no results found