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
125455241 12545524 1 I 20160706 20160711 20160711 EXP US-009507513-1607USA002998 MERCK 0.00 M Y 0.00000 20160711 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
125455241 12545524 1 PS JANUVIA SITAGLIPTIN PHOSPHATE 1 Oral U 21995 FILM-COATED TABLET

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
125455241 12545524 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125455241 12545524 Abasia
125455241 12545524 Blood glucose increased
125455241 12545524 Neuropathy peripheral
125455241 12545524 Non-alcoholic steatohepatitis

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found