Admira MR30 mg

Type 2 Diabetes Mellitus

Admira MR is an established, guideline-supported oral antidiabetic medicine indicated for the treatment of type 2 diabetes mellitus in adults, used as an adjunct to diet and exercise when these measures alone do not adequately control blood glucose. Admira MR is approved and marketed in numerous countries, including Bangladesh, as monotherapy, and Admira MR is also commonly used in combination with other oral antidiabetic agents (such as metformin, alpha-glucosidase inhibitors, or DPP-4 inhibitors) or with insulin, when glycemic control is not achieved with a single agent.

Combination Therapy

When type 2 diabetes is not adequately controlled on metformin or another single agent alone, Admira MR may be added as a second-line agent, consistent with international treatment guidelines; combination use of Admira MR with other antidiabetic drugs requires the addition of that second agent, and this goal is not achieved by Admira MR alone.

Each tablet contains Gliclazide 80 mg (conventional/immediate-release form), or Gliclazide 30 mg / 60 mg as a modified-release (MR) tablet, depending on the marketed brand and formulation.

Admira MR is an oral antidiabetic medicine belonging to the second-generation sulfonylurea class, used to help control blood glucose levels in adults with type 2 diabetes mellitus. Admira MR works mainly by stimulating the pancreas to release more insulin, and Admira MR also has additional effects on blood vessel and platelet function. Admira MR is used as an adjunct to diet, exercise, and weight management, either alone or together with other antidiabetic medicines. Admira MR does not treat type 1 diabetes and is not a substitute for insulin in patients who require it. Admira MR should be taken exactly as prescribed by a qualified healthcare professional, with regular monitoring of blood glucose.

Antidiabetic agent (Second-generation Sulfonylurea)

Gliclazide lowers blood glucose primarily by stimulating insulin secretion from pancreatic beta cells. Gliclazide binds to specific receptors on the beta-cell membrane, closing ATP-sensitive potassium channels; this depolarizes the cell membrane, opens voltage-dependent calcium channels, and increases intracellular calcium influx, which triggers insulin release by exocytosis. Gliclazide also restores the early phase of insulin secretion that is characteristically blunted in type 2 diabetes, and Gliclazide is reported to have additional hemobiological effects, including reducing platelet adhesiveness and aggregation and enhancing fibrinolytic activity, which may help lower the risk of small-vessel complications, although these effects are secondary to the primary glucose-lowering action of Gliclazide. Gliclazide is well absorbed after oral administration; the modified-release formulation of Gliclazide is designed to release the drug gradually over 24 hours to support once-daily dosing. Gliclazide is extensively metabolized in the liver to inactive metabolites and is excreted mainly in urine, with a plasma half-life of approximately 10-12 hours for conventional Gliclazide.

• Take Admira MR with or shortly before a meal (typically breakfast), never on an empty stomach, to reduce the risk of hypoglycemia.
• Swallow modified-release (MR) tablets of Admira MR whole with a glass of water; do not chew, crush, or split MR tablets of Admira MR.
• Take Admira MR at approximately the same time each day.
• If a dose of Admira MR is missed, do not take a double dose to make up for it; take the next dose of Admira MR at the usual time.
• Do not skip meals while taking Admira MR, as this increases the risk of hypoglycemia.
• Continue Admira MR exactly as prescribed and do not stop or change the dose without consulting a physician, even if blood glucose appears well controlled.

• Miconazole (systemic, including oral gel): concurrent use with Admira MR can precipitate severe hypoglycemia, including coma; concurrent use is contraindicated (see Contraindications).
• Other azole antifungals (e.g. fluconazole) and CYP2C9 inhibitors: may increase blood levels of Admira MR and increase the risk of hypoglycemia; dose adjustment and closer monitoring may be needed.
• Alcohol: can potentiate the blood-glucose-lowering effect of Admira MR and increase the risk of severe hypoglycemia; a disulfiram-like reaction has also been reported with sulfonylureas including Admira MR; alcohol should be avoided or limited.
• Beta-blockers: may mask the warning symptoms of hypoglycemia (such as tremor and palpitations) caused by Admira MR and can potentiate its glucose-lowering effect; use with caution.
• NSAIDs, ACE inhibitors, and other antidiabetic agents/insulin: may enhance the hypoglycemic effect of Admira MR; closer blood glucose monitoring is advised when these are combined with Admira MR.
• Danazol: has an inherent hyperglycemic effect that can antagonize the effect of Admira MR; concurrent use is generally avoided unless glucose monitoring is intensified.
• Corticosteroids and thiazide diuretics: can raise blood glucose and reduce the effectiveness of Admira MR; dose adjustment of Admira MR may be needed if these are started or stopped.
• Warfarin and other coumarin anticoagulants: sulfonylureas including Admira MR may potentiate anticoagulant effect; monitoring of anticoagulation is advised.

Common Side Effects

• Hypoglycemia (low blood sugar) - the most frequent and clinically important side effect of Admira MR; see Precautions and Warnings.
• Gastrointestinal disturbances such as nausea, vomiting, abdominal pain, diarrhea, or constipation.
• Mild, transient visual disturbances related to changes in blood glucose levels, especially at the start of treatment with Admira MR.

Less Common / Serious Side Effects (Seek Medical Attention)

• Skin reactions such as rash, itching, or hives caused by Admira MR; rarely, severe reactions such as Stevens-Johnson syndrome or angioedema.
• Blood disorders (rare) associated with Admira MR, including low white blood cell count, low platelet count, anemia, or pancytopenia, which may present as unusual bruising, bleeding, infections, or fatigue.
• Liver problems (rare) associated with Admira MR, including raised liver enzymes, cholestatic jaundice, or hepatitis, which may present as yellowing of the skin/eyes, dark urine, or unusual tiredness.
• Weight gain associated with Admira MR.

Pregnancy

Admira MR is generally not recommended for use in pregnancy. Sulfonylureas such as Admira MR can cross the placenta, and poorly controlled maternal blood glucose itself carries risk to the fetus; insulin is generally the preferred agent for achieving glycemic control during pregnancy because of its long safety record in this setting. If a woman taking Admira MR becomes pregnant, or is planning pregnancy, she should be switched to insulin under medical supervision. Admira MR should be used in pregnancy only if clearly needed and no suitable alternative is available, with the potential benefit weighed against potential risk to the fetus, and only under the direct guidance of a physician.

Breastfeeding

Admira MR is not recommended during breastfeeding, because of the risk of hypoglycemia in the nursing infant and a lack of adequate safety data on Admira MR in this setting. Women who need treatment for type 2 diabetes while breastfeeding should discuss alternative options, such as insulin, with their physician instead of using Admira MR.

• Hypoglycemia: Admira MR can cause hypoglycemia, particularly if meals are missed or delayed, after unusual physical exertion, with alcohol intake, or in elderly, malnourished, or renally/hepatically impaired patients. Patients taking Admira MR should be counseled to recognize symptoms of hypoglycemia (sweating, tremor, hunger, confusion, palpitations) and how to manage them (e.g., taking fast-acting glucose), and to seek urgent medical attention for severe or persistent hypoglycemia.
• Renal and hepatic impairment: Admira MR is metabolized by the liver and excreted by the kidneys; impaired function of either organ can prolong the action of Admira MR and increase the risk of hypoglycemia. Use a lower starting dose of Admira MR and monitor closely in mild-to-moderate impairment; severe impairment is a contraindication to Admira MR (see Contraindications).
• Loss of glycemic control: during periods of stress such as fever, trauma, infection, or surgery, blood glucose control with Admira MR may deteriorate, and temporary insulin therapy may be required in place of Admira MR.
• Cardiovascular considerations: some older sulfonylureas have historically been associated with a possible increase in cardiovascular mortality compared with diet alone or newer agents; this is a class-wide consideration for sulfonylureas including Admira MR, and patients with cardiovascular disease should discuss the balance of benefits and risks of Admira MR with their physician.
• Weight gain: Admira MR, like other sulfonylureas, may be associated with weight gain; this should be considered as part of overall diabetes management alongside Admira MR.
• Glucose-6-phosphate dehydrogenase (G6PD) deficiency: sulfonylureas including Admira MR may rarely cause hemolytic anemia in patients with G6PD deficiency; use Admira MR with caution in this population, and consider a non-sulfonylurea alternative where possible.
• Driving and operating machinery: hypoglycemia or hyperglycemia caused by Admira MR can impair concentration and reaction ability; patients should be cautious, especially when starting Admira MR or changing its dose.

Overdose of Admira MR can cause hypoglycemia, which may range from mild symptoms (sweating, tremor, hunger, palpitations, confusion) to severe hypoglycemia with seizures, loss of consciousness, or coma. If Admira MR overdose is suspected and the patient is conscious, give sugar or a glucose-containing drink or food immediately. Seek emergency medical attention or contact a poison control center right away, as hypoglycemia caused by Admira MR overdose, especially with modified-release formulations of Admira MR, can be severe and prolonged, requiring hospitalization, intravenous glucose administration, and extended monitoring of blood glucose (often for 24 hours or more) even after apparent recovery. Do not attempt to manage a suspected overdose of Admira MR at home without medical guidance.

Store Admira MR at room temperature (below 30°C), away from light and moisture. Keep Admira MR out of the reach and sight of children. Do not use Admira MR beyond its expiry date.

Children

The safety and efficacy of Admira MR have not been established in children and adolescents under 18 years of age. Admira MR is not recommended for use in this age group.

Elderly

Elderly patients are more susceptible to the hypoglycemic effects of Admira MR. Treatment with Admira MR should be started at the lowest available dose, with careful, gradual titration and close monitoring of blood glucose.

Renal Impairment

Patients with mild-to-moderate renal impairment should start Admira MR at a low dose with close monitoring, because reduced clearance can prolong the action of Admira MR and increase the risk of hypoglycemia. Admira MR is contraindicated in severe renal impairment.

Hepatic Impairment

Because Admira MR is extensively metabolized in the liver, patients with mild-to-moderate hepatic impairment should start Admira MR at a low dose with close monitoring. Admira MR is contraindicated in severe hepatic impairment.

Pregnant and Breastfeeding Women

See the Pregnancy and Lactation section above for detailed guidance on the use of Admira MR in this population.

Admira MR is generally used long-term, as type 2 diabetes mellitus is a chronic condition requiring ongoing management. The duration of treatment with Admira MR is determined by a physician based on periodic reassessment of blood glucose control (including HbA1c), tolerability, and the presence of any complications; Admira MR is often continued indefinitely as part of a diabetes management plan, but the dose of Admira MR may be adjusted, or Admira MR may be combined with or switched to other antidiabetic therapy, over time. Patients should not stop taking Admira MR without consulting their physician, even if they feel well, since discontinuation of Admira MR can lead to loss of blood glucose control.

Sulfonylurea (second-generation oral antidiabetic agent)

Gliclazide lowers blood glucose by binding to sulfonylurea receptors on pancreatic beta-cell membranes and closing ATP-sensitive potassium channels. This causes membrane depolarization, opening of voltage-gated calcium channels, and an influx of calcium into the beta cell, which stimulates the release of stored insulin by exocytosis. By increasing circulating insulin, Gliclazide enhances glucose uptake by peripheral tissues and reduces hepatic glucose output, thereby lowering blood glucose levels. Gliclazide is also reported to reduce platelet aggregation and adhesiveness and to increase fibrinolytic activity, effects that are considered secondary to the primary glucose-lowering action of Gliclazide.

Admira MR has not been established as safe and effective for use in children or adolescents under 18 years of age, and pediatric dosing of Admira MR has not been defined. Type 2 diabetes in children and adolescents is generally managed with other agents (such as metformin or insulin) that have established pediatric safety and efficacy data, rather than with Admira MR. Admira MR should not be used in children unless specifically directed by a pediatric specialist in exceptional circumstances.