
The first FDA-approved dual GIP and GLP-1 receptor agonist for type 2 diabetes. Once weekly.
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Yes. MOUNJARO is an FDA-approved prescription medication. A telemedicine evaluation with a licensed provider is required before a prescription can be issued.
The most common side effects are gastrointestinal: nausea, vomiting, diarrhea, constipation, and abdominal pain, typically most pronounced in the first weeks and improving as your dose is titrated. Pancreatitis has been reported — stop use and contact your provider immediately if you develop persistent, severe abdominal pain. Hypoglycemia risk increases when used with insulin or insulin secretagogues. Worsening of diabetic retinopathy has been reported. In animal studies, GIP/GLP-1 receptor agonists have been associated with thyroid C-cell tumors; contraindicated in patients with a personal or family history of medullary thyroid carcinoma or MEN 2.
Contraindicated in patients with a personal or family history of medullary thyroid carcinoma or MEN 2. Not for use during pregnancy. Use with caution in patients with a history of pancreatitis or diabetic retinopathy.
Use with caution when combined with insulin or insulin secretagogues due to hypoglycemia risk. MOUNJARO may slow gastric emptying and affect timing of oral medication absorption. Disclose all current medications to your provider.
Use with caution in patients with a history of pancreatitis, significant renal impairment, or diabetic retinopathy. Serious hypersensitivity reactions require immediate discontinuation. Full medical review is required for all patients.
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