Fitaro 1 mg Injection contains Semaglutide, a glucagon-like peptide-1 (GLP-1) receptor agonist designed for the management of type 2 diabetes mellitus. By mimicking the action of the naturally occurring incretin hormone GLP-1, Semaglutide helps regulate blood glucose levels, promotes satiety, and supports weight management in adults with type 2 diabetes.
রেজিস্টার্ড চিকিৎসকের পরামর্শ অনুযায়ী ঔষধ সেবন করুন
GLP-1 Receptor Agonist
Antidiabetic Agent
Fitaro 1 mg is indicated for:
Type 2 Diabetes Mellitus: As an adjunct to diet and exercise to improve glycemic control in adults.
Weight Management (Adjunct Therapy): May support weight reduction in overweight or obese patients with type 2 diabetes when combined with lifestyle interventions.
Semaglutide acts as a GLP-1 receptor agonist, enhancing glucose-dependent insulin secretion from pancreatic beta cells and suppressing inappropriate glucagon secretion from alpha cells. This dual action helps lower fasting and postprandial glucose levels.
Additional pharmacological effects include:
Delayed gastric emptying, reducing postprandial glucose spikes
Central appetite regulation, increasing satiety and decreasing caloric intake
Cardiovascular benefits: Semaglutide has demonstrated reduction in major adverse cardiovascular events in patients with type 2 diabetes and high cardiovascular risk.
Semaglutide is administered subcutaneously and has a prolonged half-life, allowing once-weekly dosing.
Initial Dose: 0.25 mg once weekly for the first 4 weeks (for titration).
Maintenance Dose: Increase to 0.5 mg once weekly; may further escalate to 1 mg once weekly based on glycemic response and tolerability.
Administer subcutaneously in the abdomen, thigh, or upper arm. Rotate injection sites with each dose.
Not recommended for type 1 diabetes or diabetic ketoacidosis.
Common adverse reactions:
Nausea, vomiting, diarrhea, constipation
Abdominal pain, dyspepsia
Decreased appetite, headache
Serious adverse reactions (rare):
Pancreatitis (acute or chronic)
Hypoglycemia (especially when used with sulfonylureas or insulin)
Gallbladder disorders (including cholelithiasis and cholecystitis)
Renal impairment in patients with pre-existing kidney disease
Rare hypersensitivity reactions, including anaphylaxis
Personal or family history of medullary thyroid carcinoma (MTC) or multiple endocrine neoplasia syndrome type 2 (MEN 2)
Hypersensitivity to Semaglutide or any excipients in the formulation
Monitor patients for symptoms of pancreatitis, especially with persistent abdominal pain.
Use caution in patients with gastrointestinal disease; delayed gastric emptying may worsen symptoms.
May cause mild to moderate gastrointestinal discomfort during dose escalation; gradual titration can improve tolerability.
Assess renal function periodically in patients with pre-existing kidney disease.
Pregnancy: Category C. Use only if benefits outweigh risks; avoid in breastfeeding due to unknown excretion in human milk.
Elderly: No dose adjustment necessary, but monitor for dehydration from gastrointestinal side effects.
Renal/Hepatic Impairment: No initial dose adjustment required; monitor closely for tolerability.
Store refrigerated at 2–8°C.
Protect from light.
Do not freeze.
Keep out of the reach of children.
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