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
126279311 12627931 1 I 20160711 20160801 20160807 20160807 PER US-ELI_LILLY_AND_COMPANY-US201608002286 ELI LILLY AND CO 0.00 F Y 0.00000 20160807 CN 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
126279311 12627931 1 PS HUMALOG INSULIN LISPRO 1 Unknown 4 U, EACH MORNING C392369C 20563 4 IU INJECTION QD
126279311 12627931 2 SS HUMALOG INSULIN LISPRO 1 Unknown 10 U, EACH EVENING C392369C 20563 10 IU INJECTION QD
126279311 12627931 3 C LEVEMIR INSULIN DETEMIR 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126279311 12627931 1 Type 1 diabetes mellitus

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126279311 12627931 Blood glucose abnormal
126279311 12627931 Malaise

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
126279311 12627931 1 1976 0
126279311 12627931 2 1976 0