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
127156681 12715668 1 I 2016 20160729 20160906 20160906 EXP DE-009507513-1608DEU000020 MERCK 58.00 YR M Y 0.00000 20160906 CN DE DE

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
127156681 12715668 1 PS JANUMET METFORMIN HYDROCHLORIDESITAGLIPTIN PHOSPHATE 1 Oral 50/1000MG (1 DF), TWICE A DAY N U 22044 1 DF FILM-COATED TABLET BID
127156681 12715668 2 C PANTOPRAZOLE PANTOPRAZOLE SODIUM 1 0
127156681 12715668 3 C DICLO DICLOFENAC SODIUM 1 UNK, PRN 0
127156681 12715668 4 C ORTOTON 2 UNK, PRN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127156681 12715668 1 Type 2 diabetes mellitus
127156681 12715668 2 Prophylaxis against gastrointestinal ulcer
127156681 12715668 3 Back pain
127156681 12715668 4 Pain

Outcome of event

Event ID CASEID OUTC COD
127156681 12715668 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127156681 12715668 Alanine aminotransferase increased
127156681 12715668 Aspartate aminotransferase increased
127156681 12715668 Blood elastase decreased
127156681 12715668 Diarrhoea
127156681 12715668 Weight decreased

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
127156681 12715668 1 20160405 20160705 0
127156681 12715668 3 2004 0
127156681 12715668 4 2004 0