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
126849933 12684993 3 F 2014 20160905 20160825 20160912 EXP JP-009507513-1608JPN010852 MERCK 0.00 F Y 0.00000 20160912 PH JP JP

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
126849933 12684993 1 PS JANUVIA SITAGLIPTIN PHOSPHATE 1 Oral DAILY DOSAGE UNKNOWN 21995 TABLET
126849933 12684993 2 SS JANUVIA SITAGLIPTIN PHOSPHATE 1 Oral DAILY DOSAGE UNKNOWN 21995 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126849933 12684993 1 Diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
126849933 12684993 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126849933 12684993 Interstitial lung 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
126849933 12684993 1 2012 0