Premil 0.5 mg is an oral antidiabetic medicine belonging to the meglitinide analogue class. It is indicated as an adjunct to diet and exercise for improving glycemic control in patients with type 2 diabetes mellitus (NIDDM). Premil is particularly effective in controlling postprandial blood glucose levels by stimulating rapid, short-acting insulin secretion. It can be used as monotherapy or in combination with Metformin when adequate glycemic control is not achieved with diet, exercise, and a single agent alone.
রেজিস্টার্ড চিকিৎসকের পরামর্শ অনুযায়ী ঔষধ সেবন করুন
Premil 0.5 mg is indicated for:
Type 2 diabetes mellitus (NIDDM) as an adjunct to diet and exercise
Patients whose hyperglycemia cannot be adequately controlled by diet and exercise alone
Combination therapy with Metformin in patients inadequately controlled on either Premil or Metformin monotherapy
Meglitinide Analogues
Premil 0.5 mg stimulates insulin secretion from pancreatic β-cells. It acts by inhibiting potassium (K⁺) efflux through ATP-regulated potassium channels in the β-cell membrane. This inhibition leads to membrane depolarization, opening of voltage-dependent calcium channels, and increased intracellular calcium influx. The rise in intracellular calcium triggers insulin release. The insulinotropic effect of Premil is glucose-dependent and primarily targets postprandial hyperglycemia.
Premil 0.5 mg should be taken immediately before or up to 30 minutes prior to meals.
The drug may be taken 2, 3, or 4 times daily depending on meal frequency
If a meal is skipped, the corresponding dose should also be skipped
If an extra meal is taken, an additional dose should be taken with that meal
Missed doses should not be taken between meals
Dosage Range:
0.5 mg to 4 mg before each meal
Maximum daily dose: 16 mg
Initial Dose:
HbA1c <8%: 0.5 mg before each meal
HbA1c >8% or previously treated patients: 1–2 mg before each meal
Dose adjustments should be made at 1–2 week intervals based on glycemic response.
The dose of Premil 0.5 mg may require adjustment when co-administered with other medications:
CYP450 inhibitors (e.g., azole antifungals, macrolides) may increase drug exposure
CYP450 inducers (e.g., Rifampin, Phenobarbital, Carbamazepine) may reduce efficacy
Highly protein-bound drugs (e.g., NSAIDs) may increase hypoglycemic risk
Other hypoglycemic agents and drugs such as salicylates, sulphonamides, MAO inhibitors, and beta-blockers may increase the risk of hypoglycemia
No clinically significant interaction with Digoxin, Theophylline, Warfarin, or Cimetidine
Premil 0.5 mg is contraindicated in patients with:
Diabetic ketoacidosis, with or without coma
Type 1 diabetes mellitus
Known hypersensitivity to Premil or any of its components
The most commonly reported adverse effect is hypoglycemia. Other possible side effects include:
Upper respiratory tract infections
Diarrhea or constipation
Nausea and vomiting
Hypersensitivity reactions such as rash and urticaria
The safety of Premil 0.5 mg during pregnancy has not been established. It should be used during pregnancy only if clearly needed. It is not known whether Premil is excreted in human breast milk. A decision should be made to discontinue breastfeeding or the drug, considering the importance of therapy to the mother.
Premil should always be taken with meals to reduce the risk of hypoglycemia
Insulin therapy should be considered during periods of stress such as surgery, severe infection, trauma, or myocardial infarction
All oral antidiabetic agents can cause hypoglycemia; patients should be counseled accordingly
Doses up to 80 mg have been associated primarily with glucose-lowering effects. Severe hypoglycemia, coma, or seizures are rare, particularly when meals are taken. Management is supportive, with close monitoring of blood glucose levels.
Store below 30°C. Protect from light. Keep out of reach of children.
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