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
107391003 10739100 3 F 201501 20160630 20150126 20160719 PER US-ELI_LILLY_AND_COMPANY-US201501006455 ELI LILLY AND CO 70.11 YR F Y 0.00000 20160719 OT 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
107391003 10739100 1 PS HUMALOG MIX75/25 INSULIN LISPRO 1 Unknown 24 U, EACH MORNING C311765D 20563 24 IU INJECTION QD
107391003 10739100 2 SS HUMALOG MIX75/25 INSULIN LISPRO 1 Unknown 22 U, EACH EVENING C311765D 20563 22 IU INJECTION QD
107391003 10739100 3 SS HUMALOG MIX75/25 INSULIN LISPRO 1 Unknown 24 U, EACH MORNING C310570C 20563 24 IU INJECTION QD
107391003 10739100 4 SS HUMALOG MIX75/25 INSULIN LISPRO 1 Unknown 22 U, EACH EVENING C310570C 20563 22 IU INJECTION QD
107391003 10739100 5 SS HUMALOG MIX75/25 INSULIN LISPRO 1 Unknown 36 U, EACH MORNING C467096E 20563 36 IU INJECTION QD
107391003 10739100 6 SS HUMALOG MIX75/25 INSULIN LISPRO 1 Unknown 34 U, EACH EVENING C467096E 20563 34 IU INJECTION QD
107391003 10739100 7 SS HUMALOG MIX75/25 INSULIN LISPRO 1 Unknown UNK, OTHER C447026H 20563 INJECTION
107391003 10739100 8 SS HUMALOG INSULIN LISPRO 1 Unknown UNK, PRN C311017A 0 INJECTION
107391003 10739100 9 SS HUMALOG INSULIN LISPRO 1 Unknown UNK, PRN C299490A 0 INJECTION
107391003 10739100 10 SS HUMALOG INSULIN LISPRO 1 Unknown UNK, PRN C292713A 0 INJECTION
107391003 10739100 11 C METFORMIN METFORMIN HYDROCHLORIDE 1 Unknown 1 DF, QD U 0 1 DF TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
107391003 10739100 1 Type 1 diabetes mellitus
107391003 10739100 8 Type 1 diabetes mellitus

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
107391003 10739100 Arthritis
107391003 10739100 Blood glucose increased
107391003 10739100 Incorrect drug administration duration
107391003 10739100 Incorrect product storage
107391003 10739100 Injection site pain
107391003 10739100 Malaise
107391003 10739100 Nausea
107391003 10739100 Wrong drug administered

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

no results found

Therapies reported

no results found