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
125253551 12525355 1 I 20160624 20160628 20160704 20160704 PER US-ELI_LILLY_AND_COMPANY-US201606011061 ELI LILLY AND CO 83.71 YR M Y 0.00000 20160704 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
125253551 12525355 1 PS HUMALOG INSULIN LISPRO 1 Unknown 5 U, EACH MORNING 20563 5 IU INJECTION QD
125253551 12525355 2 SS HUMALOG INSULIN LISPRO 1 Unknown 5 U, EACH EVENING 20563 5 IU INJECTION QD
125253551 12525355 3 SS HUMALOG INSULIN LISPRO 1 Unknown 5 U, EACH MORNING C494925C 20563 5 IU INJECTION QD
125253551 12525355 4 SS HUMALOG INSULIN LISPRO 1 Unknown 5 U, EACH EVENING C494925C 20563 5 IU INJECTION QD
125253551 12525355 5 C NOVOLIN N INSULIN HUMAN 1 UNK, EACH MORNING U 0 QD
125253551 12525355 6 C NOVOLIN N INSULIN HUMAN 1 UNK, EACH EVENING U 0 QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125253551 12525355 1 Type 1 diabetes mellitus

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125253551 12525355 Blood glucose increased
125253551 12525355 Drug ineffective
125253551 12525355 Hypoacusis

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
125253551 12525355 3 20160624 0
125253551 12525355 4 20160624 0