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
128003621 12800362 1 I 201103 20160923 20160930 20160930 EXP US-ELI_LILLY_AND_COMPANY-US201609009194 ELI LILLY AND CO 0.00 F Y 0.00000 20160930 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
128003621 12800362 1 PS HUMALOG MIX75/25 INSULIN LISPRO 1 Unknown 42 U, BID 20563 42 IU INJECTION BID
128003621 12800362 2 SS HUMALOG MIX75/25 INSULIN LISPRO 1 Unknown 42 U, BID 0 42 IU INJECTION BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
128003621 12800362 1 Type 2 diabetes mellitus
128003621 12800362 2 Type 2 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
128003621 12800362 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
128003621 12800362 Blood glucose increased
128003621 12800362 Cataract
128003621 12800362 Cerebrovascular accident
128003621 12800362 Eye haemorrhage
128003621 12800362 Gait disturbance
128003621 12800362 Glycosylated haemoglobin increased
128003621 12800362 Musculoskeletal stiffness
128003621 12800362 Visual impairment

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
128003621 12800362 1 2006 0