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
124945973 12494597 3 F 20160613 20160721 20160624 20160729 EXP US-009507513-1606USA008022 MERCK 51.40 YR F Y 139.68000 KG 20160729 MD 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
124945973 12494597 1 PS JANUMET METFORMIN HYDROCHLORIDESITAGLIPTIN PHOSPHATE 1 Oral 50/500 MG, UNKNOWN N 22044 FILM-COATED TABLET

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
124945973 12494597 OT
124945973 12494597 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124945973 12494597 Amylase decreased
124945973 12494597 Blood creatinine decreased
124945973 12494597 Blood glucose increased
124945973 12494597 Blood osmolarity decreased
124945973 12494597 Blood urea decreased
124945973 12494597 Diverticulum
124945973 12494597 Eosinophil count increased
124945973 12494597 Glycosylated haemoglobin increased
124945973 12494597 Hepatic cyst
124945973 12494597 Hepatic steatosis
124945973 12494597 Hiatus hernia
124945973 12494597 Hypotension
124945973 12494597 Monocyte count increased
124945973 12494597 Pancreatitis
124945973 12494597 Red blood cell count increased
124945973 12494597 Red blood cell sedimentation rate increased
124945973 12494597 Spinal osteoarthritis
124945973 12494597 Splenomegaly

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
124945973 12494597 1 20160615 0