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
125789713 12578971 3 F 20160504 20160913 20160721 20160916 EXP PHHY2016CA045639 NOVARTIS 53.57 YR M Y 0.00000 20160916 CN COUNTRY NOT SPECIFIED CA

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
125789713 12578971 1 PS GLEEVEC IMATINIB MESYLATE 1 Oral 400 MG, QD 21588 400 MG QD
125789713 12578971 2 SS GLEEVEC IMATINIB MESYLATE 1 Oral 400 MG, QD 21588 400 MG QD
125789713 12578971 3 SS GLEEVEC IMATINIB MESYLATE 1 Oral 400 MG, BID 21588 400 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125789713 12578971 1 Gastrointestinal stromal tumour

Outcome of event

Event ID CASEID OUTC COD
125789713 12578971 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125789713 12578971 Asthenia
125789713 12578971 Decreased appetite
125789713 12578971 Dyspnoea
125789713 12578971 Feeling abnormal
125789713 12578971 Gastrointestinal disorder
125789713 12578971 Haemoglobin decreased
125789713 12578971 Headache
125789713 12578971 Hepatomegaly
125789713 12578971 Hyperhidrosis
125789713 12578971 Hypopnoea
125789713 12578971 Migraine
125789713 12578971 Musculoskeletal stiffness
125789713 12578971 Nephrolithiasis
125789713 12578971 Oropharyngeal pain
125789713 12578971 Pain
125789713 12578971 Pyrexia
125789713 12578971 Viral test positive
125789713 12578971 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
125789713 12578971 1 20160304 0