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
125568241 12556824 1 I 20150623 20160714 20160714 PER US-SA-2015SA092606 AVENTIS 0.00 A M Y 0.00000 20160714 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
125568241 12556824 1 PS AMARYL GLIMEPIRIDE 1 Unknown U UNKNOWN 20496
125568241 12556824 2 SS FARXIGA DAPAGLIFLOZIN PROPANEDIOL 1 Oral U UNKNOWN 0 10 MG TABLET QD
125568241 12556824 3 SS METFORMIN METFORMIN HYDROCHLORIDE 1 Unknown U UNKNOWN 0
125568241 12556824 4 SS VICTOZA LIRAGLUTIDE 1 Unknown U UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125568241 12556824 2 Type 2 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
125568241 12556824 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125568241 12556824 Communication disorder
125568241 12556824 Confusional state
125568241 12556824 Depressed level of consciousness
125568241 12556824 Fatigue
125568241 12556824 Feeling abnormal
125568241 12556824 Impaired driving ability
125568241 12556824 Lethargy

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
125568241 12556824 2 20141113 0