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
126800331 12680033 1 I 20140703 20160815 20160824 20160824 EXP US-NOVOPROD-506205 NOVO NORDISK 52.00 YR A F Y 0.00000 20160824 MD 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
126800331 12680033 1 PS VICTOZA LIRAGLUTIDE 1 Subcutaneous 0.6 MG, SINGLE N UNKNOWN 22341 .6 MG SOLUTION FOR INJECTION
126800331 12680033 2 C LANTUS INSULIN GLARGINE 1 Subcutaneous 25U QAM + 15U QPM UNKNOWN 0
126800331 12680033 3 C INSULIN INSULIN NOS 1 Subcutaneous 7U WITH MEALS UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126800331 12680033 1 Type 1 diabetes mellitus
126800331 12680033 2 Type 1 diabetes mellitus
126800331 12680033 3 Type 1 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
126800331 12680033 DE
126800331 12680033 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126800331 12680033 Diabetic ketoacidosis
126800331 12680033 Loss of consciousness
126800331 12680033 Nausea
126800331 12680033 Off label use
126800331 12680033 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
126800331 12680033 1 20140703 20140703 0