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Ampride M 2mg/500mg Tablet SR

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Prescription Required

Marketer

Ambromide Pharma Private Limited

Salt Composition

Glimepiride (2mg) + Metformin (500mg)

Overview Ampride M 2mg/500mg Tablet SR

Diabexe Duo 2mg/500mg extended-release tablets are classified as antidiabetic medications. This dual-action formulation treats type 2 diabetes in adults by managing blood glucose. Diabexe Duo should be ingested with food, consistently at the same time daily for optimal effectiveness. Dosage is determined by your physician and may be adjusted based on blood sugar monitoring. Continued use is crucial, even with controlled blood sugar, as abrupt cessation can elevate glucose levels, risking complications such as kidney impairment, vision loss, neuropathy, and limb amputation. This medication complements a comprehensive diabetes management plan encompassing diet, exercise, and weight management, as advised by your doctor. Lifestyle choices significantly impact diabetes control. Hypoglycemia (low blood sugar) is a prevalent side effect, characterized by symptoms like sweating, dizziness, headache, and tremors. Maintain regular mealtimes and carry readily available glucose sources (sugary foods or juice). Alcohol consumption increases hypoglycemia risk and should be limited. Additional potential side effects include altered taste, nausea, diarrhea, abdominal discomfort, cephalalgia, and upper respiratory infections. Weight gain is also possible. This medication is contraindicated in type 1 diabetes, diabetic ketoacidosis, and severe hepatic or renal impairment. Prior heart conditions should be disclosed to your physician before commencing treatment. Pregnant or lactating individuals require medical consultation before use. Regular blood glucose monitoring is necessary, and your doctor may order blood tests to assess blood cell counts and liver function.

Uses of Ampride M 2mg/500mg Tablet SR

Managing Type 2 Diabetes

Major Benefits of Ampride M 2mg/500mg Tablet SR:

Consume this medication precisely as prescribed by your physician, adhering to the recommended dosage and treatment schedule. Ingest the tablet whole; avoid chewing, crushing, or fracturing it. Ampride M 2mg/500mg Extended-Release tablets should be taken with a meal.

Common Side effects of Ampride M 2mg/500mg Tablet SR:

  • Headache
  • Hypoglycemia (low blood glucose level)
  • Nausea
  • Diarrhea

How to use Ampride M 2mg/500mg Tablet SR:

Follow your doctor's instructions precisely regarding dosage and treatment length for this medication. Ingest the Ampride M 2mg/500mg Tablet SR whole; avoid crushing, chewing, or breaking it. Administer this extended-release tablet with a meal.

How Ampride M 2mg/500mg Tablet SR works:

Ampride M 2mg/500mg Extended-Release tablets contain glimepiride and metformin, two antidiabetic agents. Glimepiride, a sulfonylurea, stimulates pancreatic insulin secretion to reduce blood sugar. Metformin, a biguanide, acts by decreasing hepatic glucose production, retarding intestinal glucose uptake, and enhancing insulin responsiveness.

SAFETY ADVICE

AlcoholAlcoholUNSAFE

Concurrent use of Ampride M 2mg/500mg Tablet SR and alcohol is contraindicated.

PregnancyPregnancyCONSULT YOUR DOCTOR

The use of Ampride M 2mg/500mg SR tablets during pregnancy may pose risks. While human research is scarce, animal studies indicate potential harm to the fetus. A physician will assess the advantages against possible risks prior to prescribing. Seek medical advice.

Breast feedingBreast feedingUNSAFE

The sustained-release Ampride M 2mg/500mg tablet is contraindicated for breastfeeding mothers due to the potential for infant toxicity.

DrivingDrivingCAUTION

Driving ability can be impaired by both hypoglycemia and hyperglycemia. Refrain from driving if you experience these blood sugar imbalances.

KidneyKidneyCAUTION

Patients with kidney impairment should use Ampride M 2mg/500mg SR tablets cautiously, potentially requiring dosage modification. Consult your physician for guidance. Ampride M 2mg/500mg SR tablets are contraindicated in patients with severe kidney disease. Routine monitoring of renal function is recommended during treatment.

LiverLiverCAUTION

Individuals with liver impairment should use Ampride M 2mg/500mg SR tablets cautiously, potentially requiring dosage modification. Medical advice is essential. For those with mild to moderate liver disease, a low initial dose is typically prescribed; however, its use is contraindicated in cases of severe hepatic dysfunction.

What if you forget to take Ampride M 2mg/500mg Tablet SR :

Should you forget a dose of Ampride M 2mg/500mg SR Tablet, administer it promptly. Nevertheless, if your next scheduled dose is imminent, omit the missed dose and resume your usual dosing regimen. Avoid taking a double dose.

Facts to Know About Ampride M 2mg/500mg Tablet SR

LabelValue
Potential for Dependence None.
Type of Medication Medication for diabetes

FAQs on Ampride M 2mg/500mg Tablet SR

Retain this medication within its original, sealed container or packaging. Follow the storage guidelines provided on the packaging or label. Discard any leftover medication. Prevent access by children, pets, and others.
Ampride M 2mg/500mg Tablet SR carries a risk of lactic acidosis, a serious medical condition characterized by excessive blood lactic acid. Also termed MALA (Metformin-associated lactic acidosis), this rare adverse effect is particularly concerning for individuals with impaired kidney function, the elderly, or those who consume significant quantities of alcohol. Symptoms can manifest as muscle aches or weakness, vertigo, fatigue, cold extremities, respiratory distress, nausea, emesis, abdominal discomfort, or bradycardia. The immediate cessation of Ampride M 2mg/500mg Tablet SR and prompt medical attention are crucial should these symptoms appear.
Ampride M 2mg/500mg Extended-Release tablets contain glimepiride and metformin, a dual-action medication for managing type 2 diabetes mellitus. In adults, this combination improves glycemic control when used concurrently with a healthy diet and regular physical activity. Glimepiride enhances pancreatic insulin secretion, thus reducing blood glucose. Metformin acts by decreasing hepatic glucose production and increasing insulin responsiveness. This formulation is unsuitable for treating type 1 diabetes.
Ampride M 2mg/500mg sustained-release tablets may cause common adverse reactions including hypoglycemia, taste disturbances, nausea, abdominal pain, diarrhea, and cephalalgia. Rare but potentially severe side effects such as lactic acidosis are also possible. Prolonged administration may result in vitamin B12 deficiency.
Prolonged use of Ampride M 2mg/500mg SR tablets can lead to Vitamin B12 deficiency due to impaired Vitamin B12 absorption in the gastrointestinal tract. This deficiency, if left unaddressed, may result in anemia, neurological complications such as peripheral neuropathy (manifesting as tingling, numbness in extremities, and weakness), urinary dysfunction, cognitive changes, and ataxia. Preventive measures, recommended by some studies, include annual supplemental Vitamin B12 intake.
Indeed, Ampride M 2mg/500mg SR tablets can induce hypoglycemia. Low blood sugar may manifest as nausea, headache, irritability, hunger pangs, sweating, dizziness, tachycardia, and feelings of anxiety or tremor. The risk increases with skipped or delayed meals, alcohol consumption, excessive physical activity, or concomitant use of other antidiabetic medications. Consequently, consistent blood glucose monitoring is crucial. Carrying a readily available simple carbohydrate source, such as glucose tablets, honey, or fruit juice, is recommended.
Consuming alcohol concurrently with Ampride M 2mg/500mg SR tablets is unsafe. This combination may cause dangerously low blood sugar (hypoglycemia) and heighten the risk of lactic acidosis.
Ampride M 2mg/500mg Table...
59
MRP 72
18% off