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
125172482 12517248 2 F 201406 20160715 20160630 20160721 EXP JP-009507513-1606JPN012020 MERCK 74.00 YR M Y 78.00000 KG 20160721 MD 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
125172482 12517248 1 PS JANUVIA SITAGLIPTIN PHOSPHATE 1 Oral 50 MG, ONCE A DAY U 21995 50 MG TABLET QD
125172482 12517248 2 SS JANUVIA SITAGLIPTIN PHOSPHATE 1 Oral DAILY DOSAGE UNKNOWN U 21995 TABLET
125172482 12517248 3 SS TENELIA TENELIGLIPTIN 1 Oral 40 MG, DIVIDED DOSE FREQUENCY UNKNOWN 0 40 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125172482 12517248 1 Type 2 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
125172482 12517248 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125172482 12517248 Pemphigoid
125172482 12517248 Pruritus

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
125172482 12517248 1 201310 201507 0
125172482 12517248 3 201507 20160617 0