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
125592462 12559246 2 F 20160815 20160715 20160817 EXP US-009507513-1607USA005812 MERCK 0.00 F Y 0.00000 20160817 MD 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
125592462 12559246 1 PS JANUVIA SITAGLIPTIN PHOSPHATE 1 Oral 100 MG, UNK 21995 100 MG FILM-COATED TABLET
125592462 12559246 2 SS JANUVIA SITAGLIPTIN PHOSPHATE 1 Oral 100 MG TABLETS AND SPLIT IN HALF 21995 FILM-COATED TABLET
125592462 12559246 3 C ALBUTEROL SULFATE. ALBUTEROL SULFATE 1 U 0 INHALATION POWDER

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125592462 12559246 1 Type 2 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
125592462 12559246 HO
125592462 12559246 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125592462 12559246 Adverse event
125592462 12559246 Blood glucose increased
125592462 12559246 Clostridium difficile colitis
125592462 12559246 Dysphonia
125592462 12559246 Pneumonia
125592462 12559246 Wrong technique in product usage process

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

no results found

Therapies reported

no results found