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
126527401 12652740 1 I 20160802 20160815 20160815 PER US-ELI_LILLY_AND_COMPANY-US201608003666 ELI LILLY AND CO 0.00 F Y 0.00000 20160815 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
126527401 12652740 1 PS HUMULIN N INSULIN HUMAN 1 Unknown 32 U, EACH MORNING C464897G 18780 32 IU INJECTION QD
126527401 12652740 2 SS HUMALOG INSULIN LISPRO 1 Unknown 3 U, EACH MORNING C388133A 0 3 IU INJECTION QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126527401 12652740 1 Diabetes mellitus
126527401 12652740 2 Diabetes mellitus

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126527401 12652740 Blood glucose decreased
126527401 12652740 Bradyphrenia

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

no results found

Therapies reported

no results found