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
125487233 12548723 3 F 20160630 20160729 20160712 20160810 PER US-ELI_LILLY_AND_COMPANY-US201607002147 ELI LILLY AND CO 0.00 F Y 0.00000 20160809 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
125487233 12548723 1 PS HUMULIN R INSULIN HUMAN 1 Subcutaneous 1.4 U, PRN 18780 1.4 IU INJECTION
125487233 12548723 2 SS HUMULIN R INSULIN HUMAN 1 Subcutaneous 0.7 U, PRN C524367A 18780 .7 IU INJECTION
125487233 12548723 3 SS HUMULIN R INSULIN HUMAN 1 Subcutaneous 1.1 U, PRN C524367A 18780 1.1 IU INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125487233 12548723 1 Type 1 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
125487233 12548723 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125487233 12548723 Altered state of consciousness
125487233 12548723 Blood glucose abnormal
125487233 12548723 Blood glucose decreased
125487233 12548723 Incoherent
125487233 12548723 Wrong technique in product usage process

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
125487233 12548723 1 2015 0