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
125854871 12585487 1 I 2011 20160712 20160724 20160724 EXP US-ELI_LILLY_AND_COMPANY-US201607005190 ELI LILLY AND CO 0.00 M Y 131.50000 KG 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
125854871 12585487 1 PS HUMULIN R INSULIN HUMAN 1 Subcutaneous 50-60 U DAILY C477808A 18780 INJECTION
125854871 12585487 2 SS TRULICITY DULAGLUTIDE 1 Unknown 1.5 MG, WEEKLY (1/W) C494147A 0 1.5 MG INJECTION /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125854871 12585487 1 Diabetes mellitus
125854871 12585487 2 Diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
125854871 12585487 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125854871 12585487 Blood glucose decreased
125854871 12585487 Blood glucose increased
125854871 12585487 Constipation
125854871 12585487 Drug ineffective
125854871 12585487 Nausea
125854871 12585487 Thyroid cancer
125854871 12585487 Weight increased

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
125854871 12585487 1 2011 0