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Bydureon BCise

Bydureon BCise is a once-weekly injectable medication used to improve blood sugar control in adults with type 2 diabetes mellitus. It contains exenatide, a GLP-1 receptor agonist, in an extended-release formulation that provides continuous glucose control over a week. Bydureon BCise is typically used as part of a comprehensive treatment plan that includes diet and exercise. It may be used alone or in combination with other antidiabetic medications, but it is not recommended as the first-line treatment for type 2 diabetes.

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Frequently Asked Questions

How long does it take for Bydureon BCise to start working?
Open FAQClose FAQ

Bydureon BCise begins to work within a few hours after injection, but it may take several weeks to see the full effects on blood sugar levels due to its extended-release formulation.

Can Bydureon BCise be used with insulin?
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Bydureon BCise is not typically used with insulin. If insulin therapy is necessary, alternative options should be discussed with a healthcare provider.

What should I do if I miss a dose of Bydureon BCise?
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If you miss a dose of Bydureon BCise, take it as soon as you remember, but only if the next dose is at least 3 days away. Do not take two doses within 3 days of each other.

Is Bydureon BCise safe to use during pregnancy?
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Bydureon BCise should only be used during pregnancy if the potential benefits justify the potential risks to the fetus. Women who are pregnant or planning to become pregnant should discuss their treatment options with their healthcare provider.

Can Bydureon BCise cause weight loss?
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Yes, weight loss is a common effect of Bydureon BCise and other GLP-1 receptor agonists, likely due to its effects on appetite and satiety. Many patients experience modest weight loss while using Bydureon BCise.

Comprehensive Drug Guide

How Does Bydureon BCise Work?

Bydureon BCise works by activating the GLP-1 receptor in the body, which helps regulate blood glucose levels through several mechanisms:

  • Stimulates Insulin Secretion: Bydureon increases insulin production by the pancreas in response to elevated blood glucose levels, particularly after meals.
  • Suppresses Glucagon Release: It decreases the release of glucagon, a hormone that increases blood sugar levels, helping to prevent hyperglycemia.
  • Slows Gastric Emptying: By delaying the rate at which food leaves the stomach, Bydureon helps prevent rapid spikes in blood sugar levels after meals.
  • Promotes Satiety: Bydureon may reduce appetite, leading to potential weight loss in some patients.

What is Bydureon BCise Used For?

Type 2 Diabetes Mellitus: To improve glycemic control in adults as an adjunct to diet and exercise. It is not indicated for use in patients with type 1 diabetes or for the treatment of diabetic ketoacidosis.


Common Dosages

Bydureon BCise is available as a single-dose autoinjector, which contains an extended-release formulation of exenatide. Each auto-injector delivers a weekly dose of 2 mg of exenatide.

Administration: Bydureon BCise is administered as a subcutaneous injection using a single-dose autoinjector. It can be injected into the abdomen, thigh, or upper arm. The injection site should be rotated with each dose to avoid skin irritation.

Duration of Use: Bydureon BCise is intended for long-term use in managing type 2 diabetes. Patients should use the medication consistently each week and maintain regular follow-ups with their healthcare provider to monitor blood sugar levels and adjust treatment as necessary.


Typical Dosing

FDA Approved Indications

The typical dosage of Bydureon BCise is:

  • Standard Dose: 2 mg injected subcutaneously once every 7 days (weekly), at any time of day, with or without meals.

Who Shouldn't Take Bydureon BCise?

Bydureon BCise is contraindicated in patients with:

  • A personal or family history of medullary thyroid carcinoma (MTC) or patients with Multiple Endocrine Neoplasia syndrome type 2 (MEN 2), due to the increased risk of thyroid C-cell tumors observed in animal studies.
  • A history of severe hypersensitivity reactions to exenatide or any of the components in Bydureon BCise.
  • Severe gastrointestinal disease, including gastroparesis, as Bydureon slows gastric emptying.


Advice From The Pharmacist

Patients using Bydureon BCise should be advised to:

  • Administer the injection once weekly, on the same day each week. If a dose is missed, it should be taken as soon as possible, but only if the next dose is at least 3 days (72 hours) away. Do not take two doses within 3 days of each other.
  • Rotate injection sites with each dose to avoid skin irritation or lumps at the injection site.
  • Be aware of the potential for hypoglycemia, especially when Bydureon is used in combination with other diabetes medications like sulfonylureas or insulin. Monitor blood sugar levels regularly.
  • Store Bydureon BCise in the refrigerator until use. It can be stored at room temperature (below 86°F) for up to 4 weeks if necessary. Do not freeze the medication.
  • Report any signs of pancreatitis (such as severe abdominal pain that may radiate to the back), thyroid tumors (such as a lump in the neck), or allergic reactions (such as rash, itching, or difficulty breathing) to their healthcare provider immediately.


Side Effects of Bydureon BCise

Common Side Effects

  • Nausea (most common, especially at the beginning of treatment)
  • Vomiting
  • Diarrhea or constipation
  • Injection site reactions (such as redness, itching, or lumps)
  • Indigestion
  • Fatigue


Uncommon/Severe Side Effects

Serious side effects can include:

  • Pancreatitis: Patients should be informed of the signs and symptoms of pancreatitis and advised to seek medical attention if they experience severe abdominal pain.
  • Thyroid Tumors: Although rare, patients should be monitored for signs of thyroid tumors, particularly in those with a personal or family history of thyroid cancer.
  • Kidney Problems: Including acute kidney injury, particularly in patients with pre-existing renal impairment.

Risks and Warnings of Bydureon BCise

  • Pancreatitis: Bydureon has been associated with an increased risk of pancreatitis. Patients should be monitored for signs of pancreatitis, and the medication should be discontinued if pancreatitis is suspected.
  • Thyroid Tumors: Although the risk in humans is not well established, animal studies have shown an increased risk of thyroid C-cell tumors with GLP-1 receptor agonists. Patients should be aware of the potential risks.
  • Severe Gastrointestinal Disease: Bydureon should not be used in patients with severe gastrointestinal diseases, including gastroparesis, as it slows gastric emptying and can worsen these conditions.

Interactions with Bydureon BCise

Common Drug Interactions

Bydureon BCise may interact with other medications, including:

  • Oral Medications: Bydureon may affect the absorption of oral medications taken at the same time due to its effect on gastric emptying. Patients should take oral medications that require rapid absorption at least one hour before or three hours after injecting Bydureon.
  • Sulfonylureas and Insulin: Increased risk of hypoglycemia when used in combination. Dose adjustments of sulfonylureas or insulin may be necessary.
  • Warfarin: Bydureon may alter INR levels in patients taking warfarin, leading to an increased risk of bleeding. INR should be monitored closely when initiating or adjusting Bydureon therapy.

Patients should inform their healthcare provider of all medications and supplements they are taking to avoid potential interactions.



Alternatives to Bydureon BCise

Alternative treatments for type 2 diabetes include:

  • Other GLP-1 Receptor Agonists: Such as liraglutide (Victoza), dulaglutide (Trulicity), or semaglutide (Ozempic).
  • DPP-4 Inhibitors: Such as sitagliptin (Januvia) or saxagliptin (Onglyza), which also help regulate blood sugar levels.
  • SGLT2 Inhibitors: Such as canagliflozin (Invokana) or empagliflozin (Jardiance), which help lower blood sugar by causing the kidneys to remove sugar through the urine.
  • Insulin Therapy: For patients who require more intensive glucose control.

The choice of treatment depends on the individual’s overall health, the severity of their diabetes, and their response to previous treatments.