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
111186902 11118690 2 F 2007 20160905 20150518 20160913 EXP BR-ELI_LILLY_AND_COMPANY-BR201505001147 ELI LILLY AND CO 0.00 F Y 55.00000 KG 20160913 CN BR BR

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
111186902 11118690 1 PS HUMALOG INSULIN LISPRO 1 Subcutaneous UNK UNK, UNKNOWN U U 20563 INJECTION
111186902 11118690 2 SS HUMALOG INSULIN LISPRO 1 Subcutaneous UNK, UNKNOWN U U 0 INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
111186902 11118690 1 Type 1 diabetes mellitus
111186902 11118690 2 Type 1 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
111186902 11118690 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
111186902 11118690 Blood glucose increased
111186902 11118690 Eye haemorrhage
111186902 11118690 Injection site bruising
111186902 11118690 Injection site induration
111186902 11118690 Renal failure
111186902 11118690 Retinal detachment
111186902 11118690 Visual acuity reduced

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
111186902 11118690 1 1996 0