The Safety Rates Drug Report

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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
127553811 12755381 1 I 2016 20160825 20160916 20160916 PER US-009507513-1608USA013634 MERCK 0.00 F Y 0.00000 20160916 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
127553811 12755381 1 PS JANUVIA SITAGLIPTIN PHOSPHATE 1 Oral 100 MG, QD Y Y 21995 100 MG FILM-COATED TABLET QD
127553811 12755381 2 SS JANUVIA SITAGLIPTIN PHOSPHATE 1 Oral 100 MG, UNK Y Y 21995 100 MG FILM-COATED TABLET QD
127553811 12755381 3 C DULERA FORMOTEROL FUMARATE DIHYDRATEMOMETASONE FUROATE 1 0 PRESSURISED INHALATION, SUSPENSION
127553811 12755381 4 C GABAPENTIN. GABAPENTIN 1 0
127553811 12755381 5 C GLIPIZIDE. GLIPIZIDE 1 0
127553811 12755381 6 C LISINOPRIL. LISINOPRIL 1 0
127553811 12755381 7 C LEVOTHYROXINE SODIUM. LEVOTHYROXINE SODIUM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127553811 12755381 1 Type 2 diabetes mellitus

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127553811 12755381 Headache
127553811 12755381 Swelling

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
127553811 12755381 1 20160712 2016 0
127553811 12755381 2 2016 2016 0