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
126282581 12628258 1 I 201606 20160713 20160808 20160808 PER US-009507513-1607USA005578 MERCK 56.23 YR F Y 126.10000 KG 20160808 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
126282581 12628258 1 PS JANUMET XR METFORMIN HYDROCHLORIDESITAGLIPTIN PHOSPHATE 1 DOSE 50/100MG TABLET TWICE DAILY (BID) 22044 PROLONGED-RELEASE TABLET BID
126282581 12628258 2 C NEXIUM ESOMEPRAZOLE MAGNESIUM 1 122.5 MG, QD M81882 0 122.5 MG QD
126282581 12628258 3 C LANTUS INSULIN GLARGINE 1 25 UNITS AT NIGHT 0
126282581 12628258 4 C PROTONIX PANTOPRAZOLE SODIUM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126282581 12628258 1 Type 2 diabetes mellitus
126282581 12628258 2 Peptic ulcer
126282581 12628258 3 Type 2 diabetes mellitus

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126282581 12628258 Blood glucose increased
126282581 12628258 Diarrhoea
126282581 12628258 Incorrect dose administered
126282581 12628258 Wrong technique in product usage process

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
126282581 12628258 1 201606 0
126282581 12628258 3 201606 0