Brand Name: Glucotrol, Glucotrol XL, Minodiab
Generic Name: glipizide
Drug Class: Antidiabetics, Sulfonylureas
What Is Glipizide and How Does It Work?
Glipizide is used with a proper diet and exercise program to control high blood sugar in people with type 2 diabetes. It may also be used with other diabetes medications. Controlling high blood sugar helps prevent kidney damage, blindness, nerve problems, loss of limbs, and sexual function problems. Proper control of diabetes may also lessen your risk of a heart attack or stroke. Glipizide belongs to the class of drugs known as sulfonylureas. It lowers blood sugar by causing the release of your body's natural insulin.
Dosages of Glipizide :
Dosage Forms and Strengths
- 5 mg
- 10 mg
- 2.5 mg
- 5 mg
- 10 mg
Dosage Considerations – Should be Given as Follows:
Type 2 Diabetes Mellitus
- 5 mg orally once/day initially; increase by 2.5-5 mg as needed every several days based on blood glucose
- Maintenance range: 2.5-20 mg orally once/day or every 12 hours; not to exceed 40 mg/day
Extended-release tablets (Glucotrol XL)
- Initial: 5 mg/day orally given with breakfast; dose adjustment based on blood glucose should not be done more frequently than every 7 days
- Maintenance range: 5-10 mg orally once/day; not to exceed 20 mg/day
- 20 mg orally once/day; may increase by 10 mg/day every 2 weeks to 40 mg orally once/day; doses greater than 40 mg not recommended (may increase risk of QT prolongation)
Geriatric: Older than 60 years: Do not exceed 20 mg orally once/day
- Doses greater than 15 mg: orally divided every 12 hours recommended
- 2.5 mg orally once/day initially; increase by 2.5-5 mg/day every 1-2 weeks as determined by blood glucose response at intervals of several days
- May switch to extended release once daily tablets at the nearest equivalent total daily dose or lower end of recommended range; not to exceed 20 mg/day
Conversion From Immediate Release to Extended Release
- Administer the nearest equivalent immediate-release daily dose as extended-release tablet once daily
- Alternatively, administer 5 mg orally initially; titrate as necessary
Conversion From Long Half-Life Agents
- Observe patients carefully for 1-2 weeks when being converted from long half-life sulfonylureas to glipizide, because of potential for overlapping of hypoglycemic effects
- Current insulin dose less than 20 units: Discontinue insulin and initiate glipizide therapy at recommended dose
- Current insulin dose greater than 20 units: Decrease insulin dose by 50% and initiate glipizide at recommended dose; decrease insulin dose gradually based on patient's response
- Hepatic impairment: 2.5 mg orally once/day initially (immediate release); extended release not studied
- Renal impairment: Not studied; if GFR less than 50 mL/min, may decrease dose by 50% (suggested)
- Pediatric: Safety and efficacy not established
- Because elderly patients are susceptible to the hypoglycemic effects of glucose-lowering drugs, the question of how tightly glucose levels should be controlled in the elderly is controversial
- Recognizing hypoglycemia in elderly patients may be challenging
- Monitoring other parameters associated with cardiovascular disease, such as blood pressure and cholesterol, may be more important than normalized glycemic control
- Initial and maintenance dosing should be conservative
What Are Side Effects Associated with Using Glipizide ?
Side effects of glipizide include:
- Dermatologic reactions
- Abdominal pain
- Lightheadedness and fainting
- Gas (flatulence)
- Skin redness
- Red, bumpy rash
- Low blood sugar (hypoglycemia)
- Cholestatic jaundice and hepatitis occur rarely but may progress to liver failure
This document does not contain all possible side effects and others may occur. Check with your physician for additional information about side effects.
What Other Drugs Interact with Glipizide ?
If your doctor has directed you to use this medication, your doctor or pharmacist may already be aware of any possible drug interactions and may be monitoring you for them. Do not start, stop, or change the dosage of any medicine before checking with your doctor, health care provider or pharmacist first.
Severe Interactions of glipizide include:
Serious Interactions of glipizide include:
- aminolevulinic acid
- methyl aminolevulinate
Glipizide has moderate interactions with at least 156 different drugs.
Glipizide has mild interactions with at least 91 different drugs.
This information does not contain all possible interactions or adverse effects. Therefore, before using this product, tell your doctor or pharmacist of all the products you use. Keep a list of all your medications with you, and share this information with your doctor and pharmacist. Check with your health care professional or doctor for additional medical advice, or if you have health questions, concerns or for more information about this medicine.
What Are Warnings and Precautions for Glipizide ?
- This medication contains glipizide. Do not take Glucotrol, Glucotrol XL, or Minodiab if you are allergic to glipizide or any ingredients contained in this drug
- Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center immediately
Effects of Drug Abuse
- See "What Are Side Effects Associated with Using Glipizide ?"
- Loss of efficacy following prolonged use possible; if no contributing factors, to explain loss of efficacy identified, consider discontinuing therapy; additional antidiabetic therapy will be required.
- See "What Are Side Effects Associated with Using Glipizide ?"
- Patients with risk of severe hypoglycemia include the elderly, debilitated, or malnourished; adrenal or pituitary insufficiency; stress due to infection, fever, trauma, or surgery; concomitant use with beta-blockers or other sympatholytic agents may impair the patient's ability to recognize the signs and symptoms of hypoglycemia; use with caution
- If patient is exposed to stress (fever, trauma, infection, surgery), it may be necessary to discontinue glipizide and initiate insulin
- Use caution in hepatic/renal impairment
- Use with caution in pregnancy and lactation
- Increased risk of cardiovascular mortality suggested by product labeling but data is limited
- FDA-approved product labeling for many medications have included a broad contraindication in patients with a prior allergic reaction to sulfonamides; however, recent studies have suggested that cross-reactivity between antibiotic sulfonamides and non-antibiotic sulfonamides is unlikely to occur; increase in cardiovascular mortality suggested by product labeling but data is limited
- Hypoglycemia is more likely to occur when caloric intake is deficient, after severe or prolonged exercise, when alcohol is ingested, or when more than one glucose-lowering drug is used
- Hypoglycemia may be difficult to recognize in patients with autonomic neuropathy
- Hemolytic anemia may occur with glucose 6-phosphate dehydrogenase (G6PD) deficiency when treated with sulfonylurea agents; consider a non-sulfonylurea alternative
- Avoid using the extended-release tablets in patients with severe gastrointestinal narrowing of esophageal dysmotility
- Clinical studies have not found conclusive evidence that anti-diabetic drugs reduce macrovascular risk
- Loss of efficacy following prolonged use possible; if no contributing factors, to explain loss of efficacy identified, consider discontinuing therapy; additional antidiabetic therapy will be required
- Drug interactions overview:
- The hypoglycemic action of sulfonylureas may be potentiated by certain drugs including nonsteroidal anti-inflammatory agents, some azoles, and other drugs that are highly protein bound, salicylates, sulfonamides, chloramphenicol, probenecid, coumarins, monoamine oxidase inhibitors, quinolones and beta adrenergic blocking agents; conversely, certain drugs tend to produce hyperglycemia and may lead to loss of control, including thiazides and other diuretics, corticosteroids, phenothiazines, thyroid products, estrogens, oral contraceptives, phenytoin, nicotinic acid, sympathomimetics, calcium channel blocking drugs, and isoniazid; when co-administering glipizide with such drugs, patient should be observed closely for hypoglycemia or hyperglycemia; when such drugs are withdrawn, observe patient closely for loss of control
Pregnancy and Lactation
Use glipizide with caution during pregnancy if benefits outweigh risks. Animal studies show risk and human studies are not available, or neither animal nor human studies were done.