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
114210772 11421077 2 F 201502 20160913 20150826 20160920 EXP US-ELI_LILLY_AND_COMPANY-US201508005379 ELI LILLY AND CO 67.59 YR M Y 0.00000 20160920 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
114210772 11421077 1 PS HUMALOG INSULIN LISPRO 1 Unknown UNK UNK, UNKNOWN 20563 INJECTION
114210772 11421077 2 SS HUMALOG INSULIN LISPRO 1 Unknown 130 U, QD 20563 130 IU INJECTION QD
114210772 11421077 3 SS VANCOMYCIN VANCOMYCIN 1 Unknown 0
114210772 11421077 4 C LANTUS INSULIN GLARGINE 1 Unknown 80 U, EACH EVENING U 0 80 IU QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
114210772 11421077 1 Type 2 diabetes mellitus
114210772 11421077 3 Localised infection
114210772 11421077 4 Diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
114210772 11421077 OT
114210772 11421077 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
114210772 11421077 Blindness unilateral
114210772 11421077 Blood glucose increased
114210772 11421077 Cataract
114210772 11421077 Drug hypersensitivity
114210772 11421077 Erythema
114210772 11421077 Glycosylated haemoglobin increased
114210772 11421077 Incorrect dose administered
114210772 11421077 Increased appetite
114210772 11421077 Localised infection
114210772 11421077 Retinal tear
114210772 11421077 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
114210772 11421077 1 1990 0