Glumetza 500mg
Metformin Hydrochloride
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Glumetza is a biguanide that contains metformin hydrochloride. It is a prescription medication used in addition to diet and exercise to improve glucose control in adults with type II diabetes mellitus (T2DM). Controlling hyperglycemia prevents downstream complications such as kidney damage, loss of limbs, blindness, heart attack, stroke, or nerve problems. It is important that diabetes remains controlled to lessen the chance of related complications. Glumetza is not recommended for the treatment of type I diabetes mellitus (T1DM) or for patients with diabetic ketoacidosis.


Glumetza is an antidiabetic agent that works by decreasing basal and postprandial plasma glucose. Metformin lessens absorption of glucose in the intestine, lowers hepatic production of glucose, and increases insulin sensitivity by elevating peripheral glucose utilization. Metformin’s exact mechanism is not well understood, but a few methods have been postulated. These include inhibiting mitochondrial complex I activity, stimulating AMP-activated protein kinase (AMPK), inhibition of glucagon-induced increases in cyclic adenosine monophosphate (cAMP), decreasing activation of protein kinase A (PKA), and affecting gut microbiota. With Glumetza, insulin secretion does not change, however, all-day plasma insulin response and fasting insulin levels can decrease.


Common side effects include:

  • Diarrhea
  • Flatulence
  • Nausea and vomiting
  • Vitamin B12 deficiency
  • Dyspepsia
  • Asthenia
  • Abdominal distress
  • Headache
  • Heartburn
  • Loss of appetite
  • Bloating or gas
  • Belching
  • Fullness or loss of appetite


Lactic acidosis

There have been multiple reports of lactic acidosis with metformin use, with some being fatal cases. Onset was typically gradual with symptoms including muscle pain, abdominal pain, drowsiness, and respiratory distress. More severe cases of acidosis included symptoms such as hypothermia, hypotension, and bradyarrhythmia. The signs and symptoms were accompanied by increased blood lactate concentrations, anion gap acidosis, and an elevated lactate/pyruvate ratio. There are multiple risk factors that increase an individual’s chance of developing lactic acidosis while on metformin. Risk factors and subsequent risk reduction measures include:

  • Renal impairment – In post marketing cases, lactic acidosis caused by metformin mostly occurred in patients that had significant renal impairment. Do not use in patients with an eGFR of less than 45 mL/min/1.73 m2. Monitor eGFR annually in patients taking Glumetza. In those at greater risk for developing renal dysfunction, such as the elderly, institute more frequent monitoring of renal function.
  • Drug interactions – Be cautious when using Glumetza with other drugs influencing renal function, hemodynamics, metformin uptake, and acid-base balance to prevent the development of lactic acidosis. Consider monitoring patients more frequently.
  • Age 65 or greater – Older patients are at a higher risk for developing renal impairment. Therefore, renal function should be assessed more often in the elderly who are on Glumetza.
  • Radiological studies with contrast – Iodinated contrast agents in patients on metformin have caused acute reductions in renal function and therefore lactic acidosis. Discontinue Glumetza prior to an iodinated contrast imaging procedure in patients with an eGFR of 30 to 60 mL/min/1.73 m2, in patients with hepatic impairment, alcoholism, or heart failure, or in patients receiving intra-arterial iodinated contrast. Assess eGFR 48 hours after the procedure and reinitiate Glumetza once renal function has stabilized.
  • Surgery – Restricted food and fluids during surgical procedures can elevate the risk for volume depletion, hypotension, and renal impairment. Pause Glumetza while patients have restricted food and fluid intake.
  • Hypoxic states – Stop Glumetza when hypoxic states occur, such as in acute congestive heart failure, cardiovascular collapse, acute myocardial infarction, and sepsis.
  • Alcohol – Avoid excessive alcohol intake, as alcohol increases the effects of metformin on metabolism of lactate. Warn patients of the dangers of drinking large amounts of alcohol while on Glumetza.
  • Hepatic impairment – Patients with hepatic impairment are at higher risk of developing lactic acidosis when taking Glumetza. Do not use Glumetza if a patient exhibits signs of hepatic disease


Vitamin B12 Deficiency

Studies have shown a decrease in vitamin B12 levels with the use of metformin. Monitor hematologic measures annually and vitamin B12 parameters every 2 to 3 years for patients taking Glumetza. If abnormalities are present, manage appropriately with Glumetza discontinuation or vitamin B12 supplementation.

 Hypoglycemia with Concomitant Use of Insulin Products

Glumetza can cause hypoglycemia when used in combination with other products that lower blood glucose, such as insulin. Dose adjustments to insulin may be required to prevent development of hypoglycemia.

Macrovascular Outcomes

Decreased macrovascular risk with Glumetza has not been proven in any clinical studies.


Carbonic Anhydrase Inhibitors (CAI)

Carbonic anhydrase inhibitors can lower serum bicarbonate and cause non-anion gap metabolic acidosis. When used concomitantly with Glumetza, this combination can elevate an individual’s risk for developing lactic acidosis. Patients that are taking these drugs in combination should be frequently monitored. Examples of CAIs include topiramate and acetazolamide.

Drugs that Decrease Clearance of Glumetza

Medications that interfere with the renal elimination of metformin should be avoided. Drugs like ranolazine, dolutegravir, and cimetidine can increase a patient’s systemic exposure to metformin and elevate the risk of lactic acidosis.


Patients should avoid excessive alcohol intake. Alcohol has been shown to increase metformin’s effect on lactate metabolism, causing increased risk for lactic acidosis.

Other Drugs Affecting Glycemic Control

When used in combination with other drugs that can cause hypoglycemia, the risk for developing hypoglycemia with Glumetza is increased. Patients should be monitored for signs of hypoglycemia when on concomitant glucose-altering agents such as steroids, diuretics, and phenytoin.


The dose of Glumetza will be different for different patients. Take Glumetza exactly as your doctor tells you to take it. Typically, Glumetza is taken once daily by mouth with dinner to help reduce stomach effects. Take tablets whole and never crush, chew, or cut tablets. You may occasionally see a soft mass in your stools (bowel movement) that resembles a Glumetza tablet.

If you miss a dose of Glumetza, skip the missed dose and return to your normal dosing schedule. Do not take more than one dose of Glumetza at the same time.

Glumetza can be taken long term to control type II diabetes mellitus.

Glumetza should be taken with meals, preferably with an evening meal. This helps to decrease potential stomach or bowel side effects that may occur after initiating Glumetza.

If you take too much Glumetza, you should immediately go to the emergency room or contact the Poison Control Center.

Avoid excessive alcohol intake, as this increases one’s risk of developing lactic acidosis while on Glumetza. Do not binge drink in short periods, and you should not drink a lot of alcohol on a normal basis.

Common side effects of Glumetza include:

  • Diarrhea
  • Flatulence
  • Nausea and vomiting
  • Vitamin B12 deficiency
  • Dyspepsia
  • Asthenia
  • Abdominal distress
  • Headache
  • Heartburn
  • Loss of appetite
  • Bloating or gas
  • Belching
  • Fullness or loss of appetite

Serious side effects of Glumetza include lactic acidosis. Contact your provider immediately if you have signs and symptoms of lactic acidosis, such as:

  • Cold hands or feet
  • Dizziness or lightheadedness
  • Slow or irregular heartbeat
  • The feeling of being very tired or weak
  • Trouble breathing
  • Feeling drowsy
  • Having stomach pain, vomiting, or nausea

It is important that you tell your doctor all of the medications, vitamins, and supplements that you take. Maintain a medication list to give to your healthcare provider and pharmacist every time you get a new medicine. This is important because Glumetza may influence how other medicines work, and other medicines influence how Glumetza works.

Additionally, tell your doctor if you:

  • Have type 1 diabetes
  • Have a history of diabetic ketoacidosis or are risk for diabetic ketoacidosis
  • Have kidney problems.
  • Have liver problems.
  • Have heart problems
  • Are older than 80 years
  • Drink alcohol very often, or drink a lot of alcohol in a short period of time
  • Are taking insulin.
  • Have any other medical conditions.
  • Are pregnant or plan to become pregnant
  • Are breastfeeding or plan to breastfeed
  • Get dehydrated
  • Have surgery
  • Have a heart attack, stroke, or serious infection

Glumetza has effectively decreased glucose levels in children between the ages of 10 and 16 years with type 2 diabetes. Glumetza has not been evaluated in children less than 10 years of age. Glumetza, however, has not been studied in children. If you have questions about using Glumetza in your child, contact your doctor.

Glumetza should be stored at room temperature which is between 68°F to 77°F. Glumetza should be kept out of reach from children. Do not hold on to expired medicine or medicine that you no longer need. Ask your doctor how you should dispose of any Glumetza you do not use.