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Miglitol

  • Other glucose-lowering drugsOther glucose-lowering drugs

An alpha-glucosidase inhibitor taken with meals: it slows starch and sugar digestion in the gut and blunts the rise of glucose after eating.

Updated

Quick facts

Group
Other glucose-lowering drugs
Target
Intestinal alpha-glucosidases (maltase-glucoamylase, sucrase)
Used for
Type 2 diabetes
Key effects
Flatulence · Diarrhoea · Abdominal pain
Monitor
Post-meal and fasting glucose · Kidney function
ATC
A10BF02

No doses: the clinician sets them by the current guideline.

Mechanism of action

The figure shows miglitol in the active site of the N-terminal domain of human intestinal maltase-glucoamylase.

Target in 3D: Intestinal alpha-glucosidases (maltase-glucoamylase, sucrase). PDB structure 3L4W (RCSB PDB, public domain). View the structure at RCSB PDB

Miglitol is a glucose-like (deoxynojirimycin) molecule that competitively inhibits the alpha-glucosidases of the small-intestinal brush border. Starch and disaccharides such as sucrose are broken down and absorbed more slowly, so the post-meal glucose peak is lower. Undigested carbohydrate reaches the colon, where bacteria ferment it, causing gas and diarrhoea.

  1. Competitively blocks brush-border alpha-glucosidases
  2. Starch and sucrose are split into glucose more slowly
  3. Glucose enters the blood gradually after meals
  4. Post-meal glucose peak falls; fermentation causes gas

Indications

Adverse effects

Common

  • Flatulence
  • Diarrhoea
  • Abdominal pain
  • Skin rash

Contraindications

  • Diabetic ketoacidosis
  • Inflammatory bowel disease, colonic ulceration or partial intestinal obstruction, or predisposition to obstruction
  • Chronic intestinal disease with marked malabsorption, or conditions worsened by more intestinal gas
  • Hypersensitivity to the drug

Key interactions

Intestinal adsorbents (charcoal) and carbohydrate-splitting digestive enzyme preparations (amylase, pancreatin)
Reduce miglitol's effect; not taken together.
Propranolol and ranitidine
Their bioavailability can fall.
Digoxin
Plasma digoxin was lower in healthy volunteers (but not in a study of diabetic patients).
Insulin or sulfonylureas
Higher risk of hypoglycaemia.

What is monitored

  • Post-meal and fasting glucose, HbA1c
  • Kidney function
  • Gastrointestinal tolerance

Administration and safety

  • Oral tablet, taken with the first bite of each main meal.
  • Started low and increased gradually to limit gas and diarrhoea.
  • Hypoglycaemia (with other drugs) is treated with glucose (dextrose), not sucrose.

Pregnancy and breastfeeding

Safety in pregnancy is not established; insulin is the usual treatment for diabetes in pregnancy.

Nursing care

  • Before: bowel disease, kidney function.
  • During: gas, bloating, diarrhoea; glucose before and after meals.
  • Teach to keep glucose tablets or gel, not sugar or candy, for hypoglycaemia.
  • Teach that the tablet is skipped if the meal is skipped.

Pharmacokinetics

Absorption
Unlike acarbose it is absorbed, saturably (less at higher amounts).
Metabolism
Not metabolized.
Elimination
Excreted unchanged by the kidneys; it accumulates in kidney impairment.

Test yourself

Think of the answer, then tap the question to see it.

How should hypoglycaemia be treated in a patient on miglitol plus a sulfonylurea?

With oral glucose (dextrose), because miglitol blocks the splitting of sucrose.

How does miglitol differ from acarbose pharmacokinetically?

Miglitol is absorbed and excreted unchanged by the kidneys; acarbose is barely absorbed.

Why does miglitol cause flatulence?

Undigested carbohydrate reaches the colon, where bacteria ferment it.

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Connections

← Back to the class: Other glucose-lowering drugs

Educational content on how drugs work; not a prescribing guide and no substitute for a health professional's advice. No doses are given.

Sources: Miglitol: MedlinePlus Drug Information (MedlinePlus (U.S. National Library of Medicine), 2026); DailyMed - MIGLITOL tablet, coated (DailyMed (U.S. National Library of Medicine), 2022); Crystal complex of N-terminal Human Maltase-Glucoamylase with miglitol (RCSB Protein Data Bank, 2010).

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Representative model, for educational purposes only.