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
127914111 12791411 1 I 20140603 20160929 20160929 EXP PHHY2014CA068702 NOVARTIS 0.00 M Y 0.00000 20160929 MD CA 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
127914111 12791411 1 PS TASIGNA NILOTINIB 1 Oral 450 MG, QD 22068 450 MG CAPSULE QD
127914111 12791411 2 C TYLENOL ACETAMINOPHEN 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127914111 12791411 1 Chronic myeloid leukaemia
127914111 12791411 2 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127914111 12791411 Acne
127914111 12791411 Alopecia
127914111 12791411 Arthralgia
127914111 12791411 Hair colour changes
127914111 12791411 Pain
127914111 12791411 Pruritus
127914111 12791411 Rash

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
127914111 12791411 1 20131201 0