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
127250851 12725085 1 I 201608 20160831 20160908 20160908 EXP PHHY2016FR121233 NOVARTIS 78.00 YR M Y 0.00000 20160908 MD FR FR

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
127250851 12725085 1 PS TASIGNA NILOTINIB 1 Unknown 02 DF, QD 22068 2 DF CAPSULE QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127250851 12725085 1 Chronic myeloid leukaemia

Outcome of event

Event ID CASEID OUTC COD
127250851 12725085 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127250851 12725085 Abdominal pain
127250851 12725085 Gastrointestinal carcinoma
127250851 12725085 General physical condition abnormal
127250851 12725085 Metastasis
127250851 12725085 Second primary malignancy
127250851 12725085 Wound

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

no results found

Therapies reported

no results found