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
126410581 12641058 1 I 20160728 20160728 20160810 20160810 PER US-009507513-1608USA000213 MERCK 61.88 YR F Y 0.00000 20160810 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
126410581 12641058 1 PS JANUVIA SITAGLIPTIN PHOSPHATE 1 Oral UNK U 21995 FILM-COATED TABLET
126410581 12641058 2 C TOUJEO INSULIN GLARGINE 1 UNK U 0

Indications of drugs used

no results found

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126410581 12641058 Drug effect incomplete
126410581 12641058 Glycosylated haemoglobin increased

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

no results found

Therapies reported

no results found