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ALIMENTARY TRACT AND METABOLISM › DRUGS USED IN DIABETES › BLOOD GLUCOSE LOWERING DRUGS, EXCL. INSULINS › Combinations of oral blood glucose lowering drugs
glimepiride and pioglitazone
A10BD06
Forms & Strengths
- Tablet: 2 mg glimepiride / 30 mg pioglitazone
- Tablet: 4 mg glimepiride / 30 mg pioglitazone
Adult Dosing
- Initial dose based on previous therapy; typical starting dose is 1 tablet (2 mg/30 mg or 4 mg/30 mg) once daily with the first main meal
- Max daily dose: 8 mg glimepiride / 45 mg pioglitazone
Pediatric Dosing
- Safety and efficacy not established in pediatric patients (< 18 years)
Indications
- Adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus when treatment with both glimepiride and pioglitazone is appropriate
Mechanism of Action
- Glimepiride: Sulfonylurea that stimulates insulin secretion from pancreatic beta cells and reduces glucose output from the liver
- Pioglitazone: Thiazolidinedione that acts as an agonist for peroxisome proliferator-activated receptor-gamma (PPAR-g), improving sensitivity to insulin in muscle and adipose tissue and decreasing hepatic glucose production
Contraindications
- Hypersensitivity to glimepiride, pioglitazone, or any component
- Type 1 diabetes mellitus or diabetic ketoacidosis
- New York Heart Association (NYHA) Class III or IV heart failure
- Active bladder cancer or history of bladder cancer
Adverse Reactions
- Hypoglycemia
- Weight gain
- Edema and fluid retention
- Upper respiratory tract infection
- Headache
- Sinusitis
- Myalgia
- Bone fracture
Drug Interactions
- CYP2C8 inhibitors (e.g., gemfibrozil) significantly increase pioglitazone exposure
- CYP2C8 inducers (e.g., rifampin) decrease pioglitazone concentrations
- CYP2C9 inducers or inhibitors may alter glimepiride metabolism
- Drugs that cause hypoglycemia (e.g., insulin, GLP-1 receptor agonists) increase risk of severe hypoglycemia
- Thiazide diuretics and other medications that produce hyperglycemia may attenuate glycemic control
Curated Content: Needs Vetting Before Put to Clinical Use