Learn about BYETTA, the BYETTA Pen. Important Safety Information for BYETTA (exenatide) injection. Contraindications. BYETTA is contraindicated in. Exenatide (Byetta) is the first in a new class of incretin peptide mimetics .. Available at ; accessed October 15, 3. Meneilly. Exenatide (marketed as Byetta, Bydureon) is a glucagon-like peptide-1 receptor agonist (GLP-1 receptor agonist) medication, belonging to the group of incretin.

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The addition of Byetta to a regimen of metformin, a sulfonylurea, or both, resulted in statistically significant reductions from baseline in HbA 1c compared with patients receiving placebo added to these agents in the three controlled trials Bbyetta 7. Initiation with 5 mcg reduces the incidence and severity of gastrointestinal side effects.

Effects of 3 months of continuous subcutaneous administration of glucagon-like peptide 1 in elderly byeetta with type 2 diabetes. It is unknown whether patients with a history of pancreatitis are at increased risk for pancreatitis while using BYETTA; consider other antidiabetic therapies for these patients.

Nausea was the most frequently reported adverse reaction and occurred in a dose-dependent fashion. Each prefilled pen will deliver 60 doses to provide for 30 days of twice daily administration BID.

Dasiglucagon Glucagon Oxyntomodulin Antagonists: Food and Drug Administration.

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Bystta to free Drugs. Byetta should be initiated at 5 mcg administered twice daily BID at any time within the minute period before the morning and evening meals or before the two main meals of the day, approximately 6 hours or more apart. Use of twice-daily exenatide in basal insulin—treated patients with type 2 diabetes: All patients assigned to Byetta initially received 5 mcg BID for 4 weeks.


Patients should be advised which needle length and gauge should be used. Renal and Urinary Disorders: In the event of overdose, appropriate supportive treatment should be initiated according to the patient’s clinical signs and symptoms.

Byetta should not be administered after a meal. To view content sources and attributions, please refer to our editorial policy. Tell your healthcare provider if you have severe problems with your stomach, such as delayed emptying of your stomach gastroparesis or problems with digesting food.

The C max values increased less than proportionally over the same range. After 4 weeks, those patients assigned to Byetta had their dose increased to 10 mcg BID.

This article has been cited by other articles in PMC. Postmarketing reports of increased international normalized ratio INR sometimes associated with bleeding with concomitant use of warfarin. Because exenatide is commonly associated with gastrointestinal adverse reactions, BYETTA is not recommended in patients with severe gastrointestinal disease eg gastroparesis.

Because Byetta may induce nausea and byetfa with transient hypovolemia, treatment may worsen renal function. You may give other byetha a serious infection, or get a serious infection from them. Exenatide is not a substitute for insulin in insulin-requiring patients. The most frequently reported adverse reaction associated with Byetta, nausea, occurred in a dose-dependent fashion. Byetta slows gastric emptying, thereby reducing byettq rate at which meal-derived glucose appears in the circulation.

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Each milliliter mL contains micrograms mcg synthetic exenatide, 2. Postmarketing reports of altered renal function, including increased serum creatinine, renal impairment, worsened chronic renal failure, and acute renal failure, sometimes requiring hemodialysis and kidney transplantation. If you see several drops of Byetta leaking from the needle after the injection, you may not have received a complete dose.

Byetta – FDA prescribing information, side effects and uses

If you cannot turn the dose knob byeta from you to thesee Commonly Asked Questions, number 7, in Section 4 of this user manual. Approved Uses BYETTA is an injectable prescription medicine that may improve blood sugar glucose control in adults with type 2 diabetes, when used with diet and exercise.

All patients assigned to Byetta initially received 5 mcg BID for four weeks. Postprandial glucose was measured after a mixed meal tolerance test in 9.

Use in pediatric patients is not recommended as safety and effectiveness have not been established. Population pharmacokinetic analysis of male and female patients suggests that gender does not influence the distribution and elimination of exenatide.

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Caution should be exercised when Byetta is administered to a nursing woman.