Insulin degludec/liraglutide

Insulin degludec/liraglutide
Combination of
Insulin degludecInsulin analog
LiraglutideGlucagon-like peptide-1 receptor agonist (GLP-1)
Clinical data
Trade namesXultophy
AHFS/Drugs.comProfessional Drug Facts
License data
Pregnancy
category
Routes of
administration		Subcutaneous
ATC code
Legal status
Legal status
Identifiers
CAS Number
UNII
KEGG

Insulin degludec/liraglutide, sold under the brand name Xultophy, is a fixed-dose combination medication for the treatment of adults with type 2 diabetes to improve glycemic control in combination with diet and exercise.[4][5] It contains insulin degludec and liraglutide.[4][5] It is administered by subcutaneous injection.[4][5]

The most common side effects include hypoglycaemia (low blood glucose).[5] Side effects on the digestive system include nausea (feeling sick), diarrhea, vomiting, constipation, dyspepsia (indigestion), gastritis (inflammation of the stomach), abdominal pain (stomach ache), flatulence (wind), gastroesophageal reflux disease (passage of stomach acid back up towards the mouth), and distension (swelling) of the belly.[5]

Insulin degludec is a replacement insulin that acts in the same way as naturally produced insulin and helps glucose enter cells from the blood.[5] By controlling the level of blood glucose, the symptoms and complications of diabetes are reduced.[5] Insulin degludec is slightly different from human insulin as it is absorbed more slowly and regularly by the body after an injection and it works for a long time.[5]

Liraglutide belongs to the class of diabetes medicines known as GLP-1 receptor agonists[5] It acts in the same way as incretins (hormones produced in the gut) by increasing the amount of insulin that the pancreas releases in response to food.[5] This helps with the control of blood glucose levels.[5]

History

Insulin degludec/liraglutide was approved for medical use in the European Union in September 2014,[5] and in the United States in November 2016.[6][7]

References

  1. ↑ "Australian Public Assessment Report for insulin degludec/liraglutide" (PDF). Therapeutic Goods Administration (TGA). Australian Government. March 2021.
  2. ↑ "Summary for ARTG Entry: 328580 XULTOPHY insulin degludec 100 units/mL liraglutide 3.6 mg/mL solution for injection pre-filled pen 3 mL". Therapeutic Goods Administration (TGA). Australian Government.
  3. ↑ "Xultophy 100 units/ml insulin degludec + 3.6 mg/mL liraglutide solution for injection in a pre-filled pen - Summary of Product Characteristics (SmPC)". (emc). 8 October 2019. Retrieved 15 May 2020.
  4. 1 2 3 4 "Xultophy 100/3.6 (- insulin degludec and liraglutide injection, solution". DailyMed. 15 November 2019. Retrieved 15 May 2020.
  5. 1 2 3 4 5 6 7 8 9 10 11 12 13 "Xultophy EPAR". European Medicines Agency (EMA). Retrieved 15 May 2020. Text was copied from this source which is © European Medicines Agency. Reproduction is authorized provided the source is acknowledged.
  6. ↑ "Xultophy 100/3.6 (insulin degludec and liraglutide) Injection". U.S. Food and Drug Administration (FDA). 27 November 2017. Retrieved 15 May 2020.
  7. ↑ "Xultophy: FDA-Approved Drugs". U.S. Food and Drug Administration (FDA). 23 March 2020. Retrieved 15 May 2020.


This article is issued from Offline. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.