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buying victoza online Liraglutide, sold under the brand name Victoza among others, is a medication used to treat diabetes mellitus type 2 and obesity.^[1] In diabetes it is a less preferred agent compared to metformin.^[1][2] Its effects on long-term health outcomes like heart disease and life expectancy are unclear.^[1] [3]It is given by injection under the skin.^[1]

Common side effects include low blood sugar, nausea, dizziness, abdominal pain, and pain at the site of injection.^[1] Other serious side effects may include medullary thyroid cancer, angioedema, pancreatitis, gallbladder disease, and kidney problems.Use in pregnancy and breastfeeding is of unclear safety.^[1] Liraglutide is a glucagon-like peptide-1 receptor agonist (GLP-1 receptor agonist) also known as incretin mimetics.^[1]

Victoza was approved for medical use in the European Union in 2009, and in the United States in 2010.^[4][5] In 2018, it was the 143rd most commonly prescribed medication in the United States, with more than 4 million prescriptions.

Liraglutide is a medication used for the treatment of type 2 diabetes or obesity.^[1]

Type 2 diabetes

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Liraglutide improves control of blood glucose.^[8] As of 2017 it is unclear if incretin mimetics like liraglutide affect a person’s risk of death.^[9]

In diabetes it is a less preferred agent.^[1] It may be used in those in who metformin and another antidiabetic medication such as a sulfonylurea are not sufficient.^[2]

Obesity

Liraglutide may also be used together with diet and exercise for chronic weight management in adult patients.^[1] The body mass index (BMI) needs to be greater than 30 kg/m², or greater than 27 kg/m² together with high blood pressure, type 2 diabetes mellitus, or dyslipidemia.^[1]

Adverse effects

Thyroid cancer

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At exposures eight times greater than those used in humans, liraglutide caused a statistically significant increase in thyroid tumors in rats. The clinical relevance of these findings is unknown.^[10] In clinical trials, the rate of thyroid tumors in patients treated with liraglutide was 1.3 per 1000 patient years (4 people) compared to 1.0 per 1000 patients (1 person) in comparison groups. The sole person in the comparator group and four of the five persons in the liraglutide group had serum markers (elevated calcitonin) suggestive of pre-existing disease at baseline.^[10]

The FDA said serum calcitonin, a biomarker of medullary thyroid cancer, was slightly increased in liraglutide patients, but still within normal ranges, and it required ongoing monitoring for 15 years in a cancer registry.^[11]

Pancreatitis

In 2013, a group at Johns Hopkins reported an apparently statistically significant association between hospitalization for acute pancreatitis and prior treatment with GLP-1 derivatives (such as exenatide) and DPP-4 inhibitors (such as sitagliptin).^[12] In response, the United States FDA and the European Medicines Agency conducted a review of all available data regarding the possible connection between incretin mimetics and pancreatitis or pancreatic cancer. In a joint 2014 letter to the New England Journal of Medicine, the agencies concluded that “A pooled analysis of data from 14,611 patients with type 2 diabetes from 25 clinical trials in the sitagliptin database provided no compelling evidence of an increased risk of pancreatitis or pancreatic cancer” and “Both agencies agree that assertions concerning a causal association between incretin-based drugs and pancreatitis or pancreatic cancer, as expressed recently in the scientific literature and in the media, are inconsistent with the current data. The FDA and the EMA have not reached a final conclusion at this time regarding such a causal relationship. Although the totality of the data that have been reviewed provides reassurance, pancreatitis will continue to be considered a risk associated with these drugs until more data are available; both agencies continue to investigate this safety signal