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
125834611 12583461 1 I 20160708 20160722 20160722 EXP US-ELI_LILLY_AND_COMPANY-US201607004105 ELI LILLY AND CO 0.00 M Y 0.00000 20160721 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
125834611 12583461 1 PS HUMALOG INSULIN LISPRO 1 Unknown SLIDING SCALE, UNKNOWN 205747 INJECTION
125834611 12583461 2 SS HUMALOG INSULIN LISPRO 1 Unknown SLIDING SCALE, UNKNOWN C408156C 205747 INJECTION
125834611 12583461 3 C LANTUS INSULIN GLARGINE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125834611 12583461 1 Type 2 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
125834611 12583461 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125834611 12583461 Accidental underdose
125834611 12583461 Blood glucose increased
125834611 12583461 Hearing disability

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
125834611 12583461 1 201604 0