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
126262711 12626271 1 I 20160801 20160805 20160805 EXP US-009507513-1608USA000828 MERCK 0.00 M Y 0.00000 20160805 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
126262711 12626271 1 PS JANUVIA SITAGLIPTIN PHOSPHATE 1 Oral UNK 21995 FILM-COATED TABLET
126262711 12626271 2 SS INVOKANA CANAGLIFLOZIN 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126262711 12626271 1 Blood glucose abnormal
126262711 12626271 2 Blood glucose abnormal

Outcome of event

Event ID CASEID OUTC COD
126262711 12626271 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126262711 12626271 Diabetes mellitus inadequate control
126262711 12626271 Drug ineffective

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

no results found

Therapies reported

no results found