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
125859051 12585905 1 I 0 20160722 20160722 DIR 0.00 M N 180.00000 LBS 20160721 Y OT 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
125859051 12585905 1 PS GLEEVEC IMATINIB MESYLATE 1 Oral D D F0031 20180831 0 1 DF COATED TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125859051 12585905 1 Chronic myeloid leukaemia

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125859051 12585905 Muscle spasms
125859051 12585905 Peripheral swelling

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

Event ID CASEID RPSR COD
125859051 12585905 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
125859051 12585905 1 20140227 20160718 0