Empadus M Tablet 5 mg+500 mg is a combination of two antidiabetic medications used to treat patients with type 2 diabetes. Empagliflozin is a sodium glucose co-transporter-2 inhibitor and metformin is a biguanide.
Empadus M Tablet 5 mg+500 mg is used to treat patients with type 2 diabetes to improve blood glucose control.
Empagliflozin inhibits the well-known sodium glucose co-transporter-2(SGLT-2) enzymes, which are responsible for the reabsorption of glucose by the kidney. Empagliflozin works by preventing glucose from getting reabsorbed by the kidney thus eliminating it through the urine. Metformin on the other hand decreases the production of glucose in the liver, decreases the absorption of glucose from the intestine, and increases the sensitivity of body tissues to insulin. This combination increases the glucose excretion from the body and reduces glucose production in the liver thereby controlling blood glucose levels.
Empadus M Tablet 5 mg+500 mg usually starts working within a few days of taking it. But it can take several weeks before the full effects of the medication can be felt.
Empagliflozin is rapidly and extensively absorbed after oral administration, with a peak concentration achieved between 1.2 and 4 hours post dose. Metformin is completely absorbed throughout the gastrointestinal tract and is eliminated by the kidneys.
Empagliflozin is mainly eliminated through urine with the remainder eliminated in faeces. Metformin is eliminated from the body mainly via the kidneys.
The recommended dose of Empadus M Tablet 5 mg+500 mg is one 10 mg/1000 mg tablet once daily. The dosage can be adjusted according to the patient’s blood glucose levels and response to treatment.
Empadus M Tablet 5 mg+500 mg should be taken orally with or without food. The tablet should be swallowed whole and not be crushed or chewed.
Common side effects of Empadus M Tablet 5 mg+500 mg include diarrhea, nausea/vomiting, stomachache, joint and muscle pain and dizziness. Rare side effects include: rashes, breathing difficulties, chest pain, vision changes, fever, chills, and trembling.
Overdose of Empadus M Tablet 5 mg+500 mg can lead to lactic acidosis due to metformin accumulation. Symptoms of lactic acidosis include cramps and nausea, unusual tiredness, difficulty breathing, unusual muscle pain, and coldness.
Patients with cirrhosis, congestive heart failure, and those taking other antidiabetic medications should use Empadus M Tablet 5 mg+500 mg with caution. Patients with severe renal impairment should also be monitored closely. Patients should avoid excessive alcohol consumption while taking this medication.
Empadus M Tablet 5 mg+500 mg can interact with certain antibiotics, medications for HIV, diuretics, medications for kidney problems, other antidiabetic medications, and some herbal/dietary supplements.
Empadus M Tablet 5 mg+500 mg should be used with caution in patients with diabetic ketoacidosis, kidney or liver problems, congestive heart failure, and congestive heart failures. It should also be used with caution in patients with a history of lactic acidosis.
Empadus M Tablet 5 mg+500 mg should not be used with other antidiabetic medications, antibiotics, medications for HIV, diuretics, and some herbal/dietary supplements. Before starting Empadus M Tablet 5 mg+500 mg, it is important to inform your doctor about all the other medications you are currently taking.
It is best to take Empadus M Tablet 5 mg+500 mg on an empty stomach or with food to reduce the risk of stomach related side effects.
Empadus M Tablet 5 mg+500 mg is classified as Pregnancy Category C, meaning that it may not be safe to use during pregnancy as it could cause harm to the fetus.
It is not known whether Empadus M Tablet 5 mg+500 mg can pass into breast milk. Therefore, breastfeeding women should not take this medication without consulting their doctor.
If an overdose is suspected, the patient must seek medical help immediately. Symptoms of overdose may include drowsiness, vomiting, nausea, abdonimal pain, confusion, irregular heartbeat, respiratory failure, and coma.
Empadus M Tablet 5 mg+500 mg is contraindicated in patients with hypersensitivity to any component of the drug. It should also not be used in patients with diabetic ketoacidosis, hypersensitivity to metformin or other biguanides, impaired kidney and/or liver function, congestive heart failure, and cirrhosis.
Empadus M Tablet 5 mg+500 mg should be taken exactly as prescribed by the doctor and should not be taken in larger or smaller amounts than what is prescribed. The patient should inform the doctor if side effects occur or if the medication is not working as expected.
Empadus M Tablet 5 mg+500 mg should be stored at a temperature between 20-25°C in a tightly closed container. It should be kept away from light, heat, and moisture.
Empadus M Tablet 5 mg+500 mg has a volume of distribution of ~0.2 L/kg.
The half-life of Empadus M Tablet 5 mg+500 mg is approximately 10 hours.
The clearance rate of Empadus M Tablet 5 mg+500 mg is ~400 mL/min.
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