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Ampride M 1mg/500mg Tablet SR

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Prescription Required

Marketer

Ambromide Pharma Private Limited

Salt Composition

Glimepiride (1mg) + Metformin (500mg)

Overview Ampride M 1mg/500mg Tablet SR

Diabetam Duo 1mg/500mg Extended-Release Tablets are classified as antidiabetic medications. This dual-action formulation treats type 2 diabetes in adults by managing blood glucose levels. Diabetam Duo should be taken with meals, consistently at the same time daily for optimal effectiveness. Dosage is determined by your physician and may be adjusted based on your blood sugar readings. Continued use is crucial; discontinuation without medical consultation risks elevated blood sugar, potentially leading to kidney complications, vision impairment, neuropathy, and limb loss. Remember, this medication complements a comprehensive diabetes management plan encompassing diet, exercise, and weight management as directed by your doctor. The most frequent adverse reaction is hypoglycemia (low blood sugar). Learn to recognize symptoms like sweating, lightheadedness, headache, and tremors, and know how to manage them. Regular meals and readily available glucose sources (e.g., sugary snacks, fruit juice) are essential. Alcohol consumption elevates hypoglycemia risk and should be limited. Other possible side effects include altered taste, nausea, diarrhea, abdominal discomfort, headache, and upper respiratory infections. Weight gain may occur. This medication is contraindicated in patients with type 1 diabetes, diabetic ketoacidosis, or severe liver or kidney disease. Individuals with a history of heart conditions should inform their doctor before commencing treatment. Pregnant or lactating women require medical consultation prior to use. Regular blood glucose monitoring is necessary, and your doctor may recommend blood tests to assess blood cell counts and liver function.

Primary Ingredients of Ampride M 1mg/500mg Tablet SR

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Uses of Ampride M 1mg/500mg Tablet SR

Managing type 2 diabetes

Major Benefits of Ampride M 1mg/500mg Tablet SR:

Follow your doctor's instructions precisely regarding dosage and treatment length for Ampride M 1mg/500mg Tablet SR. Ingest the tablet whole; avoid chewing, crushing, or breaking it. Consume this medication with food.

Common Side effects of Ampride M 1mg/500mg Tablet SR:

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

How to use Ampride M 1mg/500mg Tablet SR:

Consume this medication precisely as your physician directs, adhering to the prescribed dosage and timeframe. Ingest the tablet whole; avoid chewing, crushing, or fracturing it. Ampride M 1mg/500mg Sustained-Release tablets should be administered with a meal.

How Ampride M 1mg/500mg Tablet SR works:

Ampride M, a sustained-release tablet (1mg glimepiride/500mg metformin), combines two antidiabetic agents. Glimepiride, a sulfonylurea, stimulates pancreatic insulin secretion to reduce blood sugar. Metformin, a biguanide, acts by decreasing hepatic glucose production, slowing intestinal glucose uptake, and enhancing insulin responsiveness.

SAFETY ADVICE

AlcoholAlcoholUNSAFE

Concurrent use of alcohol and Ampride M 1mg/500mg SR tablets is contraindicated.

PregnancyPregnancyCONSULT YOUR DOCTOR

Use of Ampride M 1mg/500mg SR tablets during pregnancy may pose risks. While human data is scarce, animal research indicates potential harm to a developing fetus. A physician will assess the potential advantages against any risks prior to prescription. Physician consultation is advised.

Breast feedingBreast feedingUNSAFE

Extended-release Ampride M tablets (1mg/500mg) are contraindicated for breastfeeding mothers due to potential infant toxicity.

DrivingDrivingCAUTION

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

KidneyKidneyCAUTION

Caution is advised when prescribing Ampride M 1mg/500mg SR tablets to individuals with impaired renal function; dosage modification may be necessary. Patients with severe kidney disease should not receive Ampride M 1mg/500mg SR tablets. Regular assessment of kidney function is recommended during treatment. Physician consultation is essential.

LiverLiverCAUTION

Patients with liver impairment should use Ampride M 1mg/500mg SR tablets cautiously, potentially requiring dosage modification. Consultation with a physician is advised. A reduced initial dose is typically prescribed for individuals with mild to moderate hepatic dysfunction; however, the medication is contraindicated in those with severe liver disease.

What if you forget to take Ampride M 1mg/500mg Tablet SR :

Should you forget to take your Ampride M 1mg/500mg Tablet SR, administer it immediately upon remembering. 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 1mg/500mg Tablet SR

LabelValue
Potential for Dependence None.
Medication Classification Medication for diabetes

FAQs on Ampride M 1mg/500mg Tablet SR

Retain this medication within its original, tightly sealed container or packaging. Follow the storage guidelines provided on the packaging or label. Discard any leftover medication. Prevent access by children, pets, and other individuals.
Lactic acidosis, a serious medical condition characterized by excessive blood lactic acid, is a potential consequence of taking Ampride M 1mg/500mg Tablet SR. Also termed Metformin-associated lactic acidosis (MALA), this rare but potentially harmful side effect is particularly concerning for individuals with impaired kidney function, the elderly, or those who consume substantial alcohol. Symptoms can manifest as muscle aches or weakness, vertigo, fatigue, cold extremities, respiratory distress, nausea, vomiting, abdominal pain, or bradycardia. Should any of these symptoms occur, discontinue Ampride M 1mg/500mg Tablet SR use and seek immediate medical attention.
Ampride M 1mg/500mg extended-release tablets contain glimepiride and metformin. This dual-action medication manages type 2 diabetes mellitus by regulating blood sugar. In conjunction with a healthy diet and exercise program, it effectively controls blood glucose in adults. Glimepiride stimulates insulin secretion from the pancreas, while metformin reduces hepatic glucose output and enhances insulin responsiveness. This formulation is unsuitable for type 1 diabetes.
Ampride M 1mg/500mg Tablet SR may cause common adverse reactions including low blood sugar, taste disturbances, nausea, abdominal discomfort, loose stools, 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 1mg/500mg Tablet SR can indeed lead to Vitamin B12 deficiency. This medication impairs the body's absorption of Vitamin B12 within the gastrointestinal tract. Consequently, untreated deficiency may result in anemia, neurological complications such as paresthesia in the extremities, muscle weakness, urinary dysfunction, cognitive changes, and gait instability. To mitigate these risks, supplemental Vitamin B12 intake, at a minimum of annually, is recommended by some studies.
Indeed, Ampride M 1mg/500mg SR tablets may induce hypoglycemia. This low blood sugar condition manifests as nausea, headache, irritability, hunger pangs, sweating, lightheadedness, 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, regular blood glucose monitoring is crucial. Carrying a readily available fast-acting sugar source, such as glucose tablets, honey, or fruit juice, is advisable.
Combining Ampride M 1mg/500mg SR tablets with alcohol is unsafe due to the risk of reduced blood glucose and subsequent hypoglycemia. Concurrent use also elevates the likelihood of lactic acidosis.
Ampride M 1mg/500mg Table...
53
MRP 64
17% off