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Additional Information
• Personal or family history of medullary thyroid carcinoma (MTC).
• Patients with Multiple Endocrine Neoplasia syndrome type 2 (MEN 2).
• Known serious hypersensitivity to tirzepatide or any of the excipients.
• Risk of Thyroid C-Cell Tumors: Has been observed in rodent studies. Relevance to humans unknown. Monitor patients for signs and symptoms of thyroid tumors.
• Pancreatitis: Has been reported. Discontinue promptly if pancreatitis is suspected.
• Hypoglycemia: May occur when used concomitantly with insulin secretagogues (e.g., sulfonylureas) or insulin. Consider lowering the dose of these medications.
• Acute Kidney Injury: Monitor renal function in patients with renal impairment reporting severe adverse gastrointestinal reactions.
• Severe Gastrointestinal Disease: Use may be associated with gastrointestinal adverse reactions, sometimes severe.
• May delay gastric emptying and impact the absorption of concomitantly administered oral medications.
• Use with insulin or insulin secretagogues increases the risk of hypoglycemia.
• Instruct on proper injection technique and the importance of dose titration to manage GI side effects.
• Advise patients to report symptoms of pancreatitis (persistent severe abdominal pain), thyroid tumors (lump in neck, dysphagia), or hypoglycemia.
• Counsel on the importance of a reduced-calorie diet and increased physical activity.
DescriptionZEPBOUND® (tirzepatide) 10 mg/0.5 mL prefilled syringe is a once-weekly, dual glucose-dependent insulinotropic polypeptide (GIP) and GLP-1 (glucagon-like peptide-1) receptor agonist indicated for chronic weight management in adults with obesity (BMI =30 kg/m²) or overweight (BMI =27 kg/m²) with at least one weight-related comorbidity, to be used adjunctively with a reduced-calorie diet and increased physical activity. Its novel mechanism synergistically activates both GIP and GLP-1 receptors, enhancing insulin secretion, suppressing glucagon, delaying gastric emptying, and promoting satiety within the hypothalamus, which collectively drive significant and sustained weight loss. The 10 mg dose represents a key maintenance option following a structured titration schedule from a 2.5 mg starting dose, designed to optimize gastrointestinal tolerability while achieving therapeutic efficacy.
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