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
125542162 12554216 2 F 20160819 20160713 20160825 PER US-ELI_LILLY_AND_COMPANY-US201607000759 ELI LILLY AND CO 0.00 F Y 0.00000 20160825 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
125542162 12554216 1 PS HUMALOG INSULIN LISPRO 1 Unknown UNK, UNKNOWN U U 20563 INJECTION
125542162 12554216 2 SS HUMALOG INSULIN LISPRO 1 Unknown UNK, UNKNOWN 0 INJECTION
125542162 12554216 3 SS HUMALOG INSULIN LISPRO 1 Unknown 12 U, TID C480472D 0 12 IU INJECTION TID
125542162 12554216 4 SS HUMAN INSULIN INSULIN HUMAN 1 Unknown UNK, UNKNOWN U U 0
125542162 12554216 5 C LANTUS INSULIN GLARGINE 1 UNK, EACH EVENING U 0 QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125542162 12554216 1 Product used for unknown indication
125542162 12554216 2 Diabetes mellitus
125542162 12554216 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125542162 12554216 Fatigue
125542162 12554216 Visual acuity reduced

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found