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
118688912 11868891 2 F 20151119 20151225 20160926 PER PHEH2015US026741 NOVARTIS 57.00 YR F Y 0.00000 20160926 CN US US

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
118688912 11868891 1 PS GLEEVEC IMATINIB MESYLATE 1 Unknown U 21588

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118688912 11868891 1 Chronic myeloid leukaemia

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
118688912 11868891 Decreased appetite
118688912 11868891 Diarrhoea
118688912 11868891 Disturbance in attention
118688912 11868891 Dry skin
118688912 11868891 Dysphonia
118688912 11868891 Dyspnoea
118688912 11868891 Fatigue
118688912 11868891 Feeling of body temperature change
118688912 11868891 Gastrooesophageal reflux disease
118688912 11868891 Hair texture abnormal
118688912 11868891 Headache
118688912 11868891 Insomnia
118688912 11868891 Muscle spasms
118688912 11868891 Myalgia
118688912 11868891 Nasal congestion
118688912 11868891 Nausea
118688912 11868891 Night sweats
118688912 11868891 Ocular hyperaemia
118688912 11868891 Swelling
118688912 11868891 Vomiting

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

no results found

Therapies reported

no results found