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
124969814 12496981 4 F 20160909 20160624 20160916 PER PHEH2016US015566 NOVARTIS 0.00 M Y 0.00000 20160916 OT 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
124969814 12496981 1 PS GLEEVEC IMATINIB MESYLATE 1 Unknown 21588
124969814 12496981 2 SS GLEEVEC IMATINIB MESYLATE 1 Unknown 100 MG, 3 OR 4 TIMES DAILY 21588 100 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124969814 12496981 1 Neoplasm malignant

Outcome of event

Event ID CASEID OUTC COD
124969814 12496981 DS
124969814 12496981 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124969814 12496981 Angina pectoris
124969814 12496981 Balance disorder
124969814 12496981 Chest pain
124969814 12496981 Dizziness
124969814 12496981 Dyspnoea
124969814 12496981 Headache
124969814 12496981 Hypoaesthesia
124969814 12496981 Muscle spasms
124969814 12496981 Nausea
124969814 12496981 Pain in extremity
124969814 12496981 Periorbital oedema

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

no results found

Therapies reported

no results found