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
123374292 12337429 2 F 201601 20160628 20160505 20160707 EXP US-ELI_LILLY_AND_COMPANY-US201605000382 ELI LILLY AND CO 0.00 F Y 0.00000 20160707 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
123374292 12337429 1 PS HUMALOG INSULIN LISPRO 1 Unknown 10 U, EACH MEAL 20563 10 IU INJECTION
123374292 12337429 2 SS HUMALOG INSULIN LISPRO 1 Unknown 10 U, EACH MEAL C514139D 20563 10 IU INJECTION
123374292 12337429 3 C LEVEMIR INSULIN DETEMIR 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123374292 12337429 1 Type 2 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
123374292 12337429 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123374292 12337429 Abasia
123374292 12337429 Blood glucose increased
123374292 12337429 Incorrect dose administered
123374292 12337429 Renal impairment
123374292 12337429 Therapeutic response decreased

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
123374292 12337429 1 201601 0