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
126675902 12667590 2 F 20160329 20160829 20160819 20160904 EXP PHHY2015CO104849 NOVARTIS 42.48 YR M Y 58.00000 KG 20160905 CN COUNTRY NOT SPECIFIED CO

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
126675902 12667590 1 PS TASIGNA NILOTINIB 1 Oral 2 DF, Q12H (IN THE MORNING AND IN THE NIGHT) 22068 2 DF CAPSULE Q12H
126675902 12667590 2 C ACETAMINOPHEN. ACETAMINOPHEN 1 Oral AS NEEDED U 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126675902 12667590 1 Chronic myeloid leukaemia
126675902 12667590 2 Pain

Outcome of event

Event ID CASEID OUTC COD
126675902 12667590 OT
126675902 12667590 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126675902 12667590 Abdominal infection
126675902 12667590 Abdominal pain upper
126675902 12667590 Amoebiasis
126675902 12667590 Anal pruritus
126675902 12667590 Blood phosphorus decreased
126675902 12667590 Blood potassium decreased
126675902 12667590 Bone pain
126675902 12667590 Chest pain
126675902 12667590 Chills
126675902 12667590 Decreased immune responsiveness
126675902 12667590 Diarrhoea
126675902 12667590 Headache
126675902 12667590 Malaise
126675902 12667590 Pyrexia
126675902 12667590 Vomiting
126675902 12667590 Weight decreased
126675902 12667590 Yellow skin

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
126675902 12667590 1 20120101 0