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
126389491 12638949 1 I 20160803 20160809 20160809 PER US-ELI_LILLY_AND_COMPANY-US201608004006 ELI LILLY AND CO 67.00 YR F Y 0.00000 20160809 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
126389491 12638949 1 PS HUMALOG MIX75/25 INSULIN LISPRO 1 Unknown 40 U, EACH MORNING C506933E 20563 40 IU INJECTION QD
126389491 12638949 2 SS HUMALOG MIX75/25 INSULIN LISPRO 1 Unknown 44 U, EACH EVENING 20563 44 IU INJECTION QD
126389491 12638949 3 SS HUMALOG INSULIN LISPRO 1 Unknown UNK UNK, TID Y C460618C 0 INJECTION TID
126389491 12638949 4 SS LANTUS INSULIN GLARGINE 1 Unknown UNK, BID U U 0 BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126389491 12638949 3 Type 2 diabetes mellitus
126389491 12638949 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126389491 12638949 Blood glucose increased
126389491 12638949 Glycosylated haemoglobin increased
126389491 12638949 Injection site bruising
126389491 12638949 Intercepted product selection error
126389491 12638949 Malaise

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
126389491 12638949 1 20160405 0
126389491 12638949 2 20160405 0
126389491 12638949 3 2014 20160405 0
126389491 12638949 4 201601 0