Invokana Tablet 100 mg is a medication used primarily for the management of type 2 diabetes mellitus. It belongs to a class of drugs known as sodium-glucose co-transporter 2 (SGLT2) inhibitors, which help control blood sugar levels.
Invokana Tablet 100 mg is used to:
| Brand Name | Invokana |
|---|---|
| Type | Tablet |
| Weight | 100 mg |
| Generic | Canagliflozin Hemihydrate |
| Manufacturer | Janata Traders (Mfg. by: Fresenius Kabi) |
| Available in | English বাংলা |
Invokana Tablet 100 mg works by inhibiting the sodium-glucose co-transporter 2 (SGLT2) in the kidneys. This action prevents glucose reabsorption in the renal tubules, leading to increased glucose excretion in the urine and reduced blood glucose levels.
Canagliflozin typically begins to lower blood glucose levels within a few hours of administration. The full therapeutic effects may take several weeks to become apparent as the body adjusts to the medication.
Canagliflozin is well absorbed following oral administration. The peak plasma concentration occurs approximately 1 to 2 hours after dosing. Food does not significantly affect the absorption of Canagliflozin.
Canagliflozin is primarily eliminated via the kidneys, with a significant portion of the drug being excreted in the urine. It is also metabolized by the liver, where it undergoes glucuronidation and other metabolic processes.
The standard dosage of Invokana Tablet 100 mg is:
The dosage may be adjusted based on individual patient needs, efficacy, and tolerance. It is generally recommended to start with 100 mg daily and increase to 300 mg if needed and well tolerated.
Canagliflozin is administered orally, typically in the form of tablets. It should be taken with or without food, usually once daily in the morning. Consistent daily dosing at the same time each day is recommended to maintain stable blood glucose levels.
Common side effects of Invokana Tablet 100 mg include:
Less common but serious side effects can include ketoacidosis, severe dehydration, and renal impairment.
Acute toxicity is rare but may occur with overdosing. Symptoms of overdose may include severe dehydration, hypotension, and electrolyte imbalances. Seek immediate medical attention if an overdose is suspected.
Precautions for using Canagliflozin include:
Canagliflozin may interact with other medications, including:
Use Canagliflozin with caution in patients with:
Canagliflozin may interact with drugs that affect renal function or glucose metabolism. For example:
There are no significant food interactions with Canagliflozin. It can be taken with or without food.
Canagliflozin is not recommended for use during pregnancy due to potential risks to the fetus. Alternative diabetes management options should be considered during pregnancy.
It is not known if Canagliflozin is excreted in breast milk. The use of Canagliflozin during lactation is not recommended unless clearly needed. Consult with a healthcare provider for alternatives.
In case of an overdose, symptoms may include severe dehydration, hypotension, and electrolyte imbalances. Immediate medical evaluation and treatment are necessary.
Canagliflozin is contraindicated in patients with:
Follow the prescribed dosage and administration instructions. Do not exceed the recommended dose. Regular monitoring of blood glucose levels and renal function is advised.
Store Canagliflozin at room temperature, away from moisture and direct light. Keep out of reach of children.
The volume of distribution for Canagliflozin is approximately 70 L, indicating widespread distribution throughout the body.
The elimination half-life of Canagliflozin is approximately 10 to 13 hours, allowing for once-daily dosing.
Canagliflozin is primarily cleared by the kidneys, with a smaller proportion undergoing hepatic metabolism. Renal clearance is an important factor in its overall elimination from the body.
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Dr. Md. Mahmud Alam
Urology (Urinary Bladder, Prostate, Kidney, Kidney Stone & Sex Organ) Specialist & Surgeon