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
92016485 9201648 5 F 2012 20160829 20130401 20160901 EXP PHHY2013FR030106 NOVARTIS 55.30 YR F Y 0.00000 20160901 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
92016485 9201648 1 PS TASIGNA NILOTINIB 1 Oral 600 MG, DAILY 274200 MG 22068 600 MG QD
92016485 9201648 2 C PLAVIX CLOPIDOGREL BISULFATE 1 Unknown 0
92016485 9201648 3 C KARDEGIC ASPIRIN LYSINE 1 Unknown 0
92016485 9201648 4 C TAHOR ATORVASTATIN CALCIUM 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
92016485 9201648 1 Chronic myeloid leukaemia
92016485 9201648 2 Arteriosclerosis
92016485 9201648 3 Arteriosclerosis
92016485 9201648 4 Hypercholesterolaemia

Outcome of event

Event ID CASEID OUTC COD
92016485 9201648 HO
92016485 9201648 DS
92016485 9201648 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
92016485 9201648 Amyotrophy
92016485 9201648 Fatigue
92016485 9201648 Myalgia
92016485 9201648 Pain
92016485 9201648 Peripheral arterial occlusive disease
92016485 9201648 Weight 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
92016485 9201648 1 20111017 20130218 0