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
124900422 12490042 2 F 20160530 20160726 20160622 20160805 EXP FR-ELI_LILLY_AND_COMPANY-FR201606006442 ELI LILLY AND CO 66.01 YR F Y 84.00000 KG 20160805 CN FR FR

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
124900422 12490042 1 PS TRULICITY DULAGLUTIDE 1 Subcutaneous 1.5 MG, WEEKLY (1/W) 125469 1.5 MG INJECTION /wk
124900422 12490042 2 SS METFORMIN METFORMIN HYDROCHLORIDE 1 Oral UNK UNK, UNKNOWN Y U 0
124900422 12490042 3 C GLICLAZIDE GLICLAZIDE 1 Unknown UNK UNK, UNKNOWN U U 0
124900422 12490042 4 C SULFONAMIDE UNSPECIFIED INGREDIENT 1 Unknown UNK UNK, UNKNOWN U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124900422 12490042 1 Product used for unknown indication
124900422 12490042 2 Product used for unknown indication
124900422 12490042 3 Product used for unknown indication
124900422 12490042 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
124900422 12490042 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124900422 12490042 Acute kidney injury
124900422 12490042 Diarrhoea
124900422 12490042 Lactic acidosis
124900422 12490042 Nausea
124900422 12490042 Vomiting

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
124900422 12490042 1 201604 0
124900422 12490042 2 20160530 0