Compare common side effects, interactions, warnings, and more.
Byetta
*image for illustrative purpose only
Insulin
*image for illustrative purpose only
Byetta
*image for illustrative purpose only
Insulin
*image for illustrative purpose only
Byetta® (exenatide) is a glucagon-like peptide-1 (GLP-1) receptor agonist used to improve blood sugar control in adults with type 2 diabetes by enhancing insulin secretion, slowing stomach emptying, and reducing glucagon release. Its FDA-approved indication is for the treatment of type 2 diabetes, typically alongside diet and exercise. It is not approved for use in type 1 diabetes or diabetic ketoacidosis. Byetta is available as a twice-daily injectable solution. Most common side effects include nausea, low blood sugar, vomiting, diarrhea, feeling jittery, dizziness, headache, indigestion, constipation, and weakness. Nausea usually decreases over time. Byetta has been associated with a risk of pancreatitis and should be used cautiously with other medications that affect blood sugar levels.
Insulin is a vital hormone produced by the pancreas that regulates blood sugar levels by facilitating the uptake of glucose into cells for energy production. It is essential for individuals with type 1 diabetes, who cannot produce insulin naturally, and is also used in some cases of type 2 diabetes to help control blood glucose levels when other medications are insufficient. Insulin therapy involves the administration of synthetic or animal-derived insulin, through injections or insulin pumps, and requires careful monitoring to balance blood sugar levels and avoid low blood sugar. Side effects can include low blood sugar, weight gain, and, in some cases, allergic reactions at the injection site.
Insulin has many different types and names. The information below is about brand name Humalog®, which is a type of insulin lispro (a rapid-acting insulin).
Glucagon-like peptide-1 (GLP-1) receptor agonist
Rapid acting human insulin analog
Byetta (exenatide) is indicated:
As an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus
Humalog (insulin lispro) is indicated:
To improve glycemic control in adult and pediatric patients with diabetes mellitus
Typically taken as an injection twice daily
Comes in single-patient-use prefilled pens that deliver 5 mcg or 10 mcg per dose
See the Full Prescribing Information for important administration instructions
Comes as an injection
Most common (≥5%) and occurring more frequently than placebo in clinical trials:
Nausea (usually decreases over time)
Low blood sugar
Vomiting
Diarrhea
Feeling jittery
Dizziness
Headache
Indigestion
Constipation
Weakness
Postmarketing reports with exenatide of increased international normalized ratio (INR) with concomitant use of warfarin, sometimes with bleeding
Adverse reactions associated with Humalog include:
Low blood sugar
Allergic reactions
Injection site reactions
Abnormal distribution of fat
Itch
Rash
History of severe hypersensitivity to exenatide or any of the excipients in Byetta
History of drug-induced immune-mediated thrombocytopenia from exenatide products
Drug interactions: orally administered medications, warfarin
Do not use during episodes of low blood sugar
Do not use in patients with hypersensitivity to insulin lispro or any of the excipients in Humalog
Drug interactions: Drugs that may increase the risk of low blood sugar (antidiabetic agents, ACE inhibitors, angiotensin II receptor blocking agents, disopyramide, fibrates, fluoxetine, monoamine oxidase inhibitors, pentoxifylline, pramlintide, salicylates, somatostatin analog [e.g., octreotide], sulfonamide antibiotics), drugs that may decrease the blood glucose lowering effect (atypical antipsychotics, corticosteroids, danazol, diuretics, estrogens, glucagon, isoniazid, niacin, oral contraceptives, phenothiazines, progestogens [e.g., in oral contraceptives], protease inhibitors, somatropin, sympathomimetic agents [e.g., albuterol, epinephrine, terbutaline], thyroid hormones), drugs that may increase or decrease the blood glucose lowering effect (alcohol, beta-blockers, clonidine, lithium salts, pentamidine), drugs that may blunt the signs and symptoms of low blood sugar (beta-blockers, clonidine, guanethidine, reserpine)
Never share a Byetta pen between patients, even if the needle is changed
Acute pancreatitis
Low blood sugar with concomitant use of insulin secretagogues or insulin
Acute kidney injury
Severe gastrointestinal disease
Immunogenicity: Patients may develop antibodies to exenatide
Hypersensitivity
Drug-induced immune-mediated thrombocytopenia
Acute gallbladder disease
Never share a Humalog prefilled pen, cartridge, reusable pen compatible with Lilly 3 mL cartridges, or syringe between patients, even if the needle is changed
High blood sugar or low blood sugar with changes in insulin regimen
Low blood sugar: May be life-threatening
Low blood sugar due to medication errors
Hypersensitivity reactions: May be life-threatening
Hypokalemia: May be life-threatening
Fluid retention and heart failure with concomitant use of thiazolidinediones (TZDs)
High blood sugar and ketoacidosis due to insulin pump device malfunction
*This information is from the label for brand name Byetta®. See the Full Prescribing Information for more complete information. Exenatide, the active ingredient in Byetta, may also be the active ingredient in other medications, and this information may not be accurate for all medications that include the active ingredient exenatide.
*This information is from the label for brand name Humalog®, which is a type of insulin lispro (a rapid-acting insulin). See the Full Prescribing Information for more complete information. Insulin has many different types and names, and this information may not be accurate for all medications that include insulin.
The information provided here is NOT MEDICAL ADVICE and is for informational and educational purposes only. The drug comparison tool does not determine eligibility for medications or treatments provided via the Hims/Hers platform. Consultation with a healthcare provider is required to assess suitability for any medical treatment based on individual health and medical history. All product names and associated trademarks are the property of their respective owners.