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
125610101 12561010 1 I 20160708 20160715 20160715 PER US-ELI_LILLY_AND_COMPANY-US201607004037 ELI LILLY AND CO 0.00 F Y 0.00000 20160715 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
125610101 12561010 1 PS HUMALOG INSULIN LISPRO 1 Unknown 25 U, TID C531769A 20563 25 IU INJECTION TID
125610101 12561010 2 SS HUMALOG INSULIN LISPRO 1 Unknown 25 U, TID C558466C 20563 25 IU INJECTION TID
125610101 12561010 3 C LANTUS INSULIN GLARGINE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125610101 12561010 1 Type 2 diabetes mellitus

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125610101 12561010 Blood glucose increased
125610101 12561010 Cardiac disorder
125610101 12561010 Drug ineffective
125610101 12561010 Feeling jittery
125610101 12561010 Headache
125610101 12561010 Malaise
125610101 12561010 Nausea
125610101 12561010 Pain

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
125610101 12561010 1 201212 0
125610101 12561010 2 201212 0