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
127817611 12781761 1 I 201608 20160919 20160926 20160926 PER US-ELI_LILLY_AND_COMPANY-US201609007436 ELI LILLY AND CO 0.00 F Y 0.00000 20160926 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
127817611 12781761 1 PS HUMULIN 70/30 INSULIN HUMAN 1 Unknown 50 U, EACH MORNING 18780 50 IU INJECTION QD
127817611 12781761 2 SS HUMULIN 70/30 INSULIN HUMAN 1 Unknown 50 U, EACH EVENING 18780 50 IU INJECTION QD
127817611 12781761 3 SS HUMULIN 70/30 INSULIN HUMAN 1 Unknown 50 U, EACH MORNING C571673C 18780 50 IU INJECTION QD
127817611 12781761 4 SS HUMULIN 70/30 INSULIN HUMAN 1 Unknown 50 U, EACH EVENING C571673C 18780 50 IU INJECTION QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127817611 12781761 1 Type 2 diabetes mellitus

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127817611 12781761 Blood glucose decreased
127817611 12781761 Blood glucose increased
127817611 12781761 Drug ineffective
127817611 12781761 Glycosylated haemoglobin increased

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
127817611 12781761 1 2002 0
127817611 12781761 2 2002 0