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
123305003 12330500 3 F 201604 20160909 20160504 20160919 EXP US-ELI_LILLY_AND_COMPANY-US201604007416 ELI LILLY AND CO 67.00 YR F Y 80.73000 KG 20160919 OT 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
123305003 12330500 1 PS TRULICITY DULAGLUTIDE 1 Subcutaneous UNK UNK, WEEKLY (1/W) Y C494151AA 125469 INJECTION /wk
123305003 12330500 2 SS SIMVASTATIN. SIMVASTATIN 1 Unknown UNK UNK, UNKNOWN Y 0
123305003 12330500 3 C METFORMIN METFORMIN HYDROCHLORIDE 1 Unknown 1000 MG, BID 0 1000 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123305003 12330500 1 Type 2 diabetes mellitus
123305003 12330500 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
123305003 12330500 OT
123305003 12330500 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123305003 12330500 Abdominal pain
123305003 12330500 Alanine aminotransferase increased
123305003 12330500 Back pain
123305003 12330500 Bilirubin conjugated increased
123305003 12330500 Blood alkaline phosphatase increased
123305003 12330500 Blood bilirubin increased
123305003 12330500 Dyspepsia
123305003 12330500 Gamma-glutamyltransferase increased
123305003 12330500 Rash

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
123305003 12330500 1 20160411 20160621 0
123305003 12330500 2 20160621 0