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
126352071 12635207 1 I 20160603 20160802 20160809 20160809 EXP PHHY2016MX107838 NOVARTIS 70.00 YR F Y 0.00000 20160809 CN COUNTRY NOT SPECIFIED MX

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
126352071 12635207 1 PS TASIGNA NILOTINIB 1 Unknown 200 MG, QD Y U 22068 200 MG CAPSULE QD
126352071 12635207 2 C PREDNISONE. PREDNISONE 1 Unknown U 0
126352071 12635207 3 C PRAVASTATIN. PRAVASTATIN 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126352071 12635207 1 Chronic myeloid leukaemia
126352071 12635207 2 Product used for unknown indication
126352071 12635207 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126352071 12635207 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
126352071 12635207 Drug intolerance
126352071 12635207 Drug level below therapeutic
126352071 12635207 Headache

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
126352071 12635207 1 20160603 20160720 0