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
127086771 12708677 1 I 2006 20160825 20160901 20160901 EXP US-ELI_LILLY_AND_COMPANY-US201608012702 ELI LILLY AND CO 72.23 YR F Y 0.00000 20160901 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
127086771 12708677 1 PS HUMULIN 70/30 INSULIN HUMAN 1 Unknown 60 U, EACH EVENING 18780 60 IU INJECTION QD
127086771 12708677 2 SS HUMULIN 70/30 INSULIN HUMAN 1 Unknown 50 U, EACH MORNING 18780 50 IU INJECTION QD
127086771 12708677 3 SS HUMULIN 70/30 INSULIN HUMAN 1 Unknown 60 U, EACH EVENING C543959D 18780 60 IU INJECTION QD
127086771 12708677 4 SS HUMULIN 70/30 INSULIN HUMAN 1 Unknown 50 U, EACH MORNING C543959D 18780 50 IU INJECTION QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127086771 12708677 1 Type 1 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
127086771 12708677 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127086771 12708677 Blood glucose abnormal
127086771 12708677 Blood glucose increased
127086771 12708677 Decreased appetite
127086771 12708677 Hypokinesia
127086771 12708677 Incorrect product storage
127086771 12708677 Loss of consciousness

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
127086771 12708677 1 2006 0
127086771 12708677 2 2006 0