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
123808863 12380886 3 F 20160307 20160630 20160518 20160705 EXP PHHY2016AR067361 NOVARTIS 48.00 YR M Y 0.00000 20160705 MD AR AR

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
123808863 12380886 1 PS TASIGNA NILOTINIB 1 Unknown UNK U 22068 CAPSULE
123808863 12380886 2 SS TASIGNA NILOTINIB 1 Unknown 600 MG, UNK U 22068 600 MG CAPSULE
123808863 12380886 3 SS TASIGNA NILOTINIB 1 Unknown 800 MG, QD U 22068 800 MG CAPSULE QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123808863 12380886 1 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
123808863 12380886 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123808863 12380886 Asthenia
123808863 12380886 Chest pain
123808863 12380886 Dizziness
123808863 12380886 Expired product administered
123808863 12380886 Hyperhidrosis
123808863 12380886 Incorrect dose administered
123808863 12380886 Therapeutic response decreased

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
123808863 12380886 2 201507 0
123808863 12380886 3 20160307 20160329 0