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
126341781 12634178 1 I 2014 20160804 20160809 20160809 EXP PH-009507513-1608PHL003159 MERCK 82.00 YR M Y 0.00000 20160809 CN PH PH

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
126341781 12634178 1 PS JANUVIA SITAGLIPTIN PHOSPHATE 1 Oral 1 DF, QD 21995 1 DF FILM-COATED TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126341781 12634178 1 Diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
126341781 12634178 DE
126341781 12634178 DS
126341781 12634178 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126341781 12634178 Adverse event
126341781 12634178 Death
126341781 12634178 Parkinson's disease

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
126341781 12634178 1 2014 0