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
124998492 12499849 2 F 20160513 20160623 20160627 20160704 EXP US-NOVOPROD-497412 NOVO NORDISK 52.00 YR A M Y 119.27000 KG 20160704 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
124998492 12499849 1 PS VICTOZA LIRAGLUTIDE 1 Subcutaneous 0.6 MG, QD ES6V724 22341 .6 MG SOLUTION FOR INJECTION QD
124998492 12499849 2 C GLIMEPIRIDE. GLIMEPIRIDE 1 UNK UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124998492 12499849 1 Type 2 diabetes mellitus
124998492 12499849 2 Type 2 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
124998492 12499849 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124998492 12499849 Abdominal discomfort
124998492 12499849 Anxiety
124998492 12499849 Asthenia
124998492 12499849 Blood glucose increased
124998492 12499849 Blood potassium decreased
124998492 12499849 Diarrhoea
124998492 12499849 Dyspnoea
124998492 12499849 Musculoskeletal discomfort
124998492 12499849 Nausea
124998492 12499849 Pruritus
124998492 12499849 Speech disorder
124998492 12499849 Tremor
124998492 12499849 Vomiting

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
124998492 12499849 1 20160503 0