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
121663583 12166358 3 F 201507 20160715 20160309 20160719 PER US-ELI_LILLY_AND_COMPANY-US201602003693 ELI LILLY AND CO 30.44 YR F Y 0.00000 20160719 MD 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
121663583 12166358 1 PS HUMULIN N INSULIN HUMAN 1 Unknown 38 U, EACH MORNING C245968C 18780 38 IU INJECTION QD
121663583 12166358 2 SS HUMULIN N INSULIN HUMAN 1 Unknown 40 U, EACH EVENING C245968C 18780 40 IU INJECTION QD
121663583 12166358 3 SS HUMALOG INSULIN LISPRO 1 Unknown UNK, UNKNOWN 0 INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121663583 12166358 1 Type 1 diabetes mellitus
121663583 12166358 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
121663583 12166358 Drug dose omission
121663583 12166358 Expired product administered
121663583 12166358 Exposure during pregnancy

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
121663583 12166358 1 201507 0
121663583 12166358 2 201507 0