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
126631441 12663144 1 I 20151027 0 20160817 20160817 DIR 15.00 YR M N 175.00000 LBS 20160816 N 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
126631441 12663144 1 PS HUMALOG INSULIN LISPRO 1 Subcutaneous GIVEN INTO/UNDER THE SKIN Y Y 0
126631441 12663144 3 C NOVOLOG IN OMNIPOD PUMP 2 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126631441 12663144 1 Type 1 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
126631441 12663144 HO
126631441 12663144 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126631441 12663144 Blood glucose increased
126631441 12663144 Contraindicated product administered
126631441 12663144 Documented hypersensitivity to administered product
126631441 12663144 Malaise
126631441 12663144 Syncope
126631441 12663144 Urticaria
126631441 12663144 Vomiting

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
126631441 12663144 1 20050401 20151026 0