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
124035523 12403552 3 F 20160225 20160726 20160525 20160729 PER US-009507513-1605USA010723 MERCK 77.21 YR M Y 133.79000 KG 20160729 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
124035523 12403552 1 PS JANUVIA SITAGLIPTIN PHOSPHATE 1 Oral 100 MG, ONCE Y L038682 21995 100 MG FILM-COATED TABLET 1X
124035523 12403552 2 SS JANUVIA SITAGLIPTIN PHOSPHATE 1 Y 21995 FILM-COATED TABLET
124035523 12403552 3 C GLIPIZIDE. GLIPIZIDE 1 20 MG, BID U 0 20 MG BID
124035523 12403552 4 C METFORMIN METFORMIN HYDROCHLORIDE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124035523 12403552 1 Diabetes mellitus
124035523 12403552 2 Glycosylated haemoglobin increased

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124035523 12403552 Blood glucose 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
124035523 12403552 1 20160225 20160225 0