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
126894921 12689492 1 I 0 20160825 20160825 DIR 79.00 YR F N 0.00000 20160824 N 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
126894921 12689492 1 PS GLEEVEC IMATINIB MESYLATE 1 Oral 0 400 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126894921 12689492 1 Mastocytosis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126894921 12689492 Joint swelling
126894921 12689492 Vomiting

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

Event ID CASEID RPSR COD
126894921 12689492 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
126894921 12689492 1 20160817 0