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Glitenly (Metformin)

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Glitenly also increases your body's response to insulin, a natural substance that controls the amount of glucose in the blood. Glitenly is used alone or with other medications, including insulin, to treat type 2 diabetes. Glitenly is in a class of drugs called biguanides.

Other names for this medication:
Avimet, Bemet, Bestoglim, Chromet, Conformin, Diamin, Diavista, Diform, Dmbest, Enselin, Eumet, Fortamet, Gamaze, Glatix, Glibetic, Glidiet, Glimkap, Glumetza, Gluoformin, Glyformin, Glymep, Glynase, Gremet, Iscept, Jalra, Medformin, Melmet, Mesite, Metanorm, Metchek, Metglib, Metica, Metmin, Metsig, Metsmall, Obimet, Osimet, Piokap, Reglide, Resicon, Risicon, Sumet, Triglucored, Volabay, Zetfor, Zinimet, Zomelis, Zomet

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Also known as: Metformin


Glitenly is a famous medication which provides treatment type 2 diabetes. Glitenly acts controlling and decreasing glucose (sugar in blood). Glitenly is oral antihyperglycemic drug from the biguanide class. Glitenly is also known as Metformin, Phage, Riomet, Fortamet, Glumetza, Obimet, Dianben, Diabex, Diaformin. Glitenly is not taken to treat type 1 diabetes. You can normally take insulin while using Glitenly. Generic name of Glitenly is Metformin. Brand names of Glitenly are Glitenly XR, Fortamet, Riomet, Glitenly, Glumetza, Diaformin, Diabex.


Usual Adult Dose for Diabetes Type 2:

Immediate-release: Initial dose: 500 mg orally twice a day or 850 mg orally once a day Dose titration: Increase in 500 mg weekly increments or 850 mg every 2 weeks as tolerated Maintenance dose: 2000 mg daily in divided doses Maximum dose: 2550 mg/day Extended-release: Initial dose: 500 to 1000 mg orally once a day Dose titration: Increase in 500 mg weekly increments as tolerated Maintenance dose: 2000 mg daily Maximum dose: 2500 mg daily Comments: -Metformin, if not contraindicated, is the preferred initial pharmacologic agent for treatment of type 2 diabetes mellitus. -Immediate-release: Take in divided doses 2 to 3 times a day with meals; titrate slowly to minimize gastrointestinal side effects. In general, significant responses are not observed with doses less than 1500 mg/day. -Extended-release: Take with the evening meal; if glycemic control is not achieved with 2000 mg once a day, may consider 1000 mg of extended-release product twice a day; if glycemic control is still not achieve, may switch to immediate-release product. Use: To improve glycemic control in adults with type 2 diabetes mellitus as an adjunct to diet and exercise.

Usual Pediatric Dose for Diabetes Type 2:

10 years or older: Immediate-release: Initial dose: 500 mg orally twice a day Dose titration: Increase in 500 mg weekly increments as tolerated Maintenance dose: 2000 mg daily Maximum dose: 2000 mg daily Comments: Take in divided doses 2 to 3 times a day with meals. Titrate slowly to minimize gastrointestinal side effects. Safety and effectiveness of Glitenly extended-release has not been established in pediatric patients less than 18 years of age. Use: To improve glycemic control in children with type 2 diabetes mellitus as an adjunct to diet and exercise.

Detailed Glitenly dosage information


Seek emergency medical attention or call the Poison Help line at 1-800-222-1222. An overdose can cause severe hypoglycemia or lactic acidosis.


Store at room temperature between 15 and 30 degrees C (59 and 86 degrees F) away from moisture, light and heat. Throw away any unused medicine after the expiration date. Keep out of the reach of children.

Side effects

The most common side effects associated with Glitenly are:

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Side effect occurrence does not only depend on medication you are taking, but also on your overall health and other factors.


You should not use Glitenly if you are allergic to metformin, or if you have:

severe kidney disease; or metabolic acidosis or diabetic ketoacidosis (call your doctor for treatment).

If you need to have surgery or any type of x-ray or CT scan using a dye that is injected into your veins, you may need to temporarily stop taking Glitenly. Be sure your caregivers know ahead of time that you are using this medication.

Tell your doctor if you have ever had:

kidney disease (your kidney function may need to be checked before you take this medicine); high ketone levels in your blood or urine; heart disease, congestive heart failure; liver disease; or if you also use insulin, or other oral diabetes medications.

You may develop lactic acidosis, a dangerous build-up of lactic acid in your blood. This may be more likely if you have other medical conditions, a severe infection, chronic alcoholism, or if you are 65 or older. Ask your doctor about your risk.

Follow your doctor's instructions about using Glitenly if you are pregnant or you become pregnant. Controlling diabetes is very important during pregnancy, and having high blood sugar may cause complications in both the mother and the baby. Tell your doctor if you become pregnant while taking Glitenly.

Metformin may stimulate ovulation in a premenopausal woman and may increase the risk of unintended pregnancy. Talk to your doctor about your risk.

You should not breastfeed while using this medicine.

Glitenly should not be given to a child younger than 10 years old. Glitenly XR is not approved for use by anyone younger than 18 years old.

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Ballistic-protective body armor and helmets are not infallible, even when they are not perforated, and can even cost of zyprexa without insurance be at the origin of injuries, either due to missile impact, or to the blast. Specific processes amenable to study include the provision of preventive services, physician and nurse technical and interpersonal care and adherence to clinical practice guidelines. Training of phlebotomists can play a pivotal role in overcoming these issues. MHC class I molecules are an essential cell surface component involved in Theileria parva sporozoite binding to bovine lymphocytes. We carry out analytical perturbation analysis on the combined model to determine the relative effects of dispersal and demographic traits and wind statistics on the spread of an invasive tree. The results suggest that a detailed examination of the temporal sequence of neuronal death in the entorhinal cortex and in extra-entorhinal areas is likely to benefit our understanding of the pathophysiology of temporal lobe epilepsy.

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