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
125574413 12557441 3 F 20160803 20160714 20160815 EXP PHHY2016CO013865 NOVARTIS 0.00 F Y 81.00000 KG 20160815 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
125574413 12557441 1 PS TASIGNA NILOTINIB 1 Oral 2 DF, BID (2 IN THE MORNING AND 2 AT NIGHT) 22068 2 DF CAPSULE BID
125574413 12557441 2 C INTERFERON ALFA-2B INTERFERON ALFA-2B 1 Unknown 2.5 IU, QW3 (MONDAY, WEDNESDAY, FRIDAY) N 0 2.5 IU TIW
125574413 12557441 3 C LEVOTHYROXINE. LEVOTHYROXINE 1 Unknown 75 MG, QD (FASTING) U 0 75 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125574413 12557441 1 Chronic myeloid leukaemia
125574413 12557441 2 Product used for unknown indication
125574413 12557441 3 Thyroid disorder

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125574413 12557441 Arthralgia
125574413 12557441 Gastritis
125574413 12557441 Headache
125574413 12557441 Hypersensitivity
125574413 12557441 Pruritus
125574413 12557441 Rash generalised
125574413 12557441 Suppressed lactation
125574413 12557441 Temperature intolerance

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
125574413 12557441 1 20151010 0
125574413 12557441 2 201506 201510 0