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Sitalor M 500 Tablet

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Prescription Required

Marketer

Baylor Pharmaceutical Pvt Ltd

Salt Composition

Sitagliptin (50mg) + Metformin (500mg)

Overview Sitalor M 500 Tablet

Diabex Duo 500mg tablets combine two medications to effectively manage elevated blood glucose in individuals with type 2 diabetes. This dual action helps prevent serious diabetic complications, such as vision impairment and kidney disease, and may lessen the risk of cardiovascular events like stroke or heart attack. Diabex Duo 500mg may be used as a standalone treatment or in conjunction with other diabetes therapies. Optimal results are achieved when combined with a balanced diet and consistent exercise. Dosage is personalized based on your health status, blood glucose readings, and other medications. Taking it with food minimizes stomach upset. Consistent daily dosing at the same time maximizes efficacy; discontinue only under your physician's guidance. Adherence to your doctor's prescribed diet and exercise plan is crucial for diabetes control; lifestyle significantly impacts management. Common side effects include nausea, vomiting, diarrhea, abdominal discomfort, headache, and sore throat. Low blood sugar (hypoglycemia) is a potential side effect, especially when used with insulin or sulfonylureas; learn to identify and manage this. This medication isn't for everyone. Inform your doctor of any history of liver, kidney, or heart disease, pancreatic issues, or significant alcohol consumption before starting. Pregnant or breastfeeding individuals should seek medical advice before use. Interactions with other medications are possible; disclose all medications to your doctor. Alcohol should be limited due to its potential to lower blood glucose. Your doctor will monitor kidney function and blood sugar levels throughout treatment.

Primary Ingredients of Sitalor M 500 Tablet

The information is unavailable.

Uses of Sitalor M 500 Tablet

Managing type 2 diabetes

Major Benefits of Sitalor M 500 Tablet:

Consume this medication precisely as directed by your physician, adhering to the prescribed dosage and timeframe. Ingest the tablet whole; avoid chewing, crushing, or fracturing it. It's recommended to take Sitalor M 500 Tablet with a meal.

Common Side effects of Sitalor M 500 Tablet:

  • Decreased appetite
  • Vomiting
  • Upper respiratory tract infection
  • Hypoglycemia (low blood glucose level)
  • Abdominal bloating
  • Nausea
  • Diarrhea

How to use Sitalor M 500 Tablet:

Consume this medication precisely as directed by your physician, adhering to both the prescribed dosage and treatment length. Ingest the tablet whole; avoid chewing, crushing, or fracturing it. Sitalor M 500 Tablets should be administered with a meal.

How Sitalor M 500 Tablet works:

Sitalor M 500 tablets contain sitagliptin and metformin, working synergistically to manage blood glucose levels. Sitagliptin enhances insulin production by the pancreas, improves insulin utilization, and decreases hepatic glucose output. Metformin, a biguanide, reduces liver glucose production, slows intestinal glucose absorption, and enhances insulin sensitivity. This dual action leads to improved glycemic control.

SAFETY ADVICE

AlcoholAlcoholUNSAFE

Concurrent alcohol and Sitalor M 500 Tablet ingestion is contraindicated.

PregnancyPregnancyCONSULT YOUR DOCTOR

The use of Sitalor M 500 Tablet during pregnancy may pose risks. While human data is scarce, animal research indicates potential harm to the fetus. A physician will assess the advantages against possible risks prior to prescribing. Seek medical advice.

Breast feedingBreast feedingCONSULT YOUR DOCTOR

Based on limited available evidence in humans, the use of Sitalor M 500 Tablet while breastfeeding may pose a risk to the infant. The medication might transfer to breast milk, potentially causing harm to the nursing child.

DrivingDrivingCAUTION

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

KidneyKidneyCAUTION

Patients with kidney impairment should use Sitalor M 500 Tablets cautiously, potentially requiring dosage modification. Consult a physician for guidance. Sitalor M 500 Tablets are contraindicated in patients with severe kidney disease. Routine monitoring of renal function is recommended during treatment.

LiverLiverUNSAFE

Individuals with liver conditions should likely refrain from using Sitalor M 500 Tablets due to potential safety risks. Medical advice is recommended.

What if you forget to take Sitalor M 500 Tablet :

Should you forget a Sitalor M 500 Tablet dose, take it immediately. Nevertheless, if your next dose is imminent, omit the missed dose and resume your usual dosing regimen. Avoid taking a double dose.

Facts to Know About Sitalor M 500 Tablet

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

FAQs on Sitalor M 500 Tablet

Sitagliptin and Metformin, combined as Sitalor M 500 Tablet, manage type 2 diabetes mellitus in adults. This medication enhances blood sugar control when coupled with a healthy diet and regular physical activity. Metformin reduces liver glucose output and increases insulin responsiveness. Sitagliptin works by suppressing DPP4, thereby boosting pancreatic insulin secretion. This formulation is unsuitable for individuals under 18.
Prolonged Sitalor M 500 Tablet use can indeed lead to Vitamin B12 deficiency by disrupting its gastric absorption. This deficiency, if left unaddressed, may result in anemia and neurological complications, manifesting as tingling or numbness in the extremities, generalized weakness, urinary dysfunction, cognitive changes, and impaired balance (ataxia). Preventive measures, according to some studies, include supplemental Vitamin B12 intake at least annually.
Sitalor M 500 Tablet may cause common side effects including low blood sugar (hypoglycemia), taste disturbances, nausea, abdominal pain, diarrhea, headache, and upper respiratory infections. Rare but serious adverse reactions such as lactic acidosis are also possible. Prolonged use might result in vitamin B12 deficiency.
Patients with hypersensitivity to any Sitalor M 500 Tablet ingredient or inactive component should not use this medication. Similarly, its use is contraindicated in individuals experiencing severe renal or hepatic dysfunction, congestive heart failure, lactic acidosis, or diabetic ketoacidosis.
Combining Sitalor M 500 Tablet and alcohol is unsafe due to a heightened risk of lactic acidosis.
Store this medication in its original, tightly sealed container or packaging, following all storage instructions provided on the label. Discard any leftover medication. Prevent access by children, pets, and others.
Sitalor M 500 Tablet use may result in lactic acidosis, a serious medical condition characterized by excessive blood lactic acid. Also termed Metformin-associated lactic acidosis (MALA), this rare complication is linked to metformin and thus contraindicated in individuals with kidney impairment, advanced age, or significant alcohol consumption. Lactic acidosis symptoms can include muscle aches or weakness, lightheadedness, fatigue, cold extremities, shortness of breath, nausea, vomiting, abdominal discomfort, or bradycardia. Should these symptoms arise, discontinue Sitagliptin + Metformin and seek immediate medical attention.
Sitagliptin and Metformin, combined as Sitalor M 500 Tablet, manage type 2 diabetes mellitus in adults. This medication enhances blood sugar control when coupled with a healthy diet and physical activity. Metformin reduces liver glucose output and improves insulin responsiveness. Sitagliptin's action involves DPP4 enzyme inhibition, boosting pancreatic insulin secretion. This formulation is unsuitable for individuals under 18.
Sitalor M 500 Tablet may cause common side effects including low blood sugar (hypoglycemia), taste changes, nausea, abdominal pain, diarrhea, headache, and upper respiratory infections. Rare but potentially serious side effects such as lactic acidosis may occur. Prolonged use can result in vitamin B12 deficiency.
Patients with hypersensitivity to any Sitalor M 500 Tablet ingredient or additive should not use this medication. Similarly, its use is contraindicated in individuals experiencing severe renal or hepatic dysfunction, congestive heart failure, lactic acidosis, or diabetic ketoacidosis.
Combining Sitalor M 500 Tablet with alcohol is unsafe and may heighten the risk of lactic acidosis.
Sitalor M 500 Tablet use may result in lactic acidosis, a serious medical condition characterized by excessive blood lactic acid. Also termed Metformin-associated lactic acidosis (MALA), this rare adverse effect necessitates caution in individuals with pre-existing kidney disease, the elderly, or those consuming significant alcohol. Symptoms such as muscle aches or weakness, vertigo, fatigue, cold extremities, dyspnea, nausea, emesis, abdominal discomfort, or bradycardia warrant immediate discontinuation of Sitagliptin + Metformin and prompt medical attention.
Indeed, prolonged Sitalor M 500 Tablet consumption can lead to vitamin B12 deficiency by disrupting its gastric absorption. Untreated, this deficiency may manifest as anemia and neurological issues, including paresthesia in the extremities, generalized weakness, urinary dysfunction, cognitive changes, and ataxia. To mitigate these risks, supplemental vitamin B12 intake, at least annually, is recommended by some investigators.
Maintain this medication within its original, securely sealed container. Follow the storage guidelines printed on the packaging. Discard any remaining medicine. Prevent access by children, pets, and others.
Sitagliptin and Metformin, combined as Sitalor M 500 Tablet, manage type 2 diabetes mellitus in adults. This medication enhances blood sugar control when used with a healthy diet and exercise regimen. Metformin reduces hepatic glucose production and improves insulin responsiveness. Sitagliptin's action involves DPP4 enzyme inhibition, thereby boosting pancreatic insulin secretion. This formulation is unsuitable for individuals under 18.
Sitalor M 500 Tablet may cause common side effects including low blood sugar (hypoglycemia), taste changes, nausea, abdominal pain, diarrhea, headache, and upper respiratory infections. Rare but serious side effects such as lactic acidosis are also possible. Prolonged use might result in vitamin B12 deficiency.
Patients with hypersensitivity to any Sitalor M 500 Tablet ingredient or additive should not use this medication. Its use is contraindicated in individuals with severely compromised kidney or liver function, congestive heart failure, lactic acidosis, or diabetic ketoacidosis.
Combining Sitalor M 500 Tablet with alcohol is unsafe and may heighten the risk of lactic acidosis.
Sitalor M 500 Tablet use may result in lactic acidosis, a serious medical condition characterized by excessive blood lactic acid. Also termed Metformin-associated lactic acidosis (MALA), this is an uncommon side effect of metformin, prompting its avoidance in individuals with pre-existing kidney issues, the elderly, or those consuming significant alcohol. Lactic acidosis symptoms can manifest as muscle aches or weakness, lightheadedness, fatigue, cold extremities, shortness of breath, nausea, vomiting, abdominal pain, or bradycardia. Should these symptoms appear, discontinue Sitagliptin + Metformin and seek immediate medical attention.
Prolonged Sitalor M 500 Tablet consumption can indeed lead to Vitamin B12 deficiency by disrupting its gastrointestinal absorption. This deficiency, if left unaddressed, may result in anemia and neurological complications. Symptoms can include paresthesia in the extremities, generalized weakness, urinary dysfunction, cognitive changes, and ataxia. To mitigate these risks, supplemental Vitamin B12 intake, at a minimum of once annually, is recommended by some studies.
Maintain this medication within its original, sealed container. Follow the storage guidelines provided on the packaging. Discard any remaining medicine. Prevent access by children, pets, and other individuals.
Sitalor M 500 Tablet
142
MRP 165
13% off