Tegazel Tablet 6 mg is an orally administered, small neutral synthetic molecule designed to act as a partial receptor agonist of the 5-HT4 receptor on both the myenteric plexus of the gastrointestinal (GI) tract and the peripheral nervous system. It is indicated for the symptomatic treatment of women aged 18 years or older suffering from irritable bowel syndrome with constipation (IBS-C) and the treatment of chronic constipation.
Tegazel Tablet 6 mg is indicated for the symptomatic treatment of women aged 18 years or older suffering from irritable bowel syndrome with constipation (IBS-C) and the treatment of chronic constipation.
| Brand Name | Tegazel |
|---|---|
| Type | Tablet |
| Weight | 6 mg |
| Generic | Tegaserod |
| Manufacturer | Healthcare Pharmaceuticals Ltd. |
| Available in | English বাংলা |
Tegazel Tablet 6 mg works directly on the 5-HT4 receptor, which is found in the myenteric plexus of the gastrointestinal tract and also in the peripheral nervous system. Once activated, the 5-HT4 receptor triggers an increase in GI motility, accelerates transit through the colon, and increases secretion of water and electrolytes in order to soften the stool and facilitate defecation.
Studies of Tegazel Tablet 6 mg indicate that the onset of improvement in symptoms following treatment generally occurs within 1 to 2 weeks. Improvement continues over the course of treatment.
Tegazel Tablet 6 mg is rapidly absorbed with peak plasma concentrations achieved in about 1 hour after oral administration. The bioavailability of Tegazel Tablet 6 mg is estimated to be around 80%.
Tegazel Tablet 6 mg is eliminated mainly via the urine. The elimination half-life of Tegazel Tablet 6 mg is approximately 11 hours.
The recommended dose of Tegazel Tablet 6 mg for the symptomatic treatment of irritable bowel syndrome with constipation (IBS-C) in adult women is 6 mg once daily taken orally with or without food. For the treatment of chronic constipation in adult women, the recommended dose is 12 mg once daily taken orally with or without food. The tablets should be swallowed whole with fluids.
Tegazel Tablet 6 mg should be taken orally, with or without food, every day at the same time. The tablets should be swallowed whole with fluids.
Common side effects associated with Tegazel Tablet 6 mg include abdominal pain, nausea, diarrhea, flatulence, headache, indigestion, vomiting, and dizziness. Less common side effects include anorexia, dyspepsia, depression, and dysgeusia.
Tegazel Tablet 6 mg is generally well tolerated with few side effects reported. There has been no evidence of developmental, reproductive, or other long-term toxicity reported with Tegazel Tablet 6 mg.
Tegazel Tablet 6 mg should be used with caution in patients with renal or hepatic impairment. In addition, Tegazel Tablet 6 mg should be used with caution in patients with neurological or cardiovascular disorders, and those taking medications that are substrates for CYP3A4 or inhibitors or inducers of CYP3A4.
Tegazel Tablet 6 mg may interact with medications that are substrates of CYP3A4 as well as medications that inhibit or induce CYP3A4 activity. Drug-drug interactions should be considered prior to starting therapy with Tegazel Tablet 6 mg.
Tegazel Tablet 6 mg should be used with caution in patients with renal or hepatic impairment, as well as those with neurological or cardiovascular disorders. Patients with these conditions should be monitored closely while on Tegazel Tablet 6 mg therapy.
Tegazel Tablet 6 mg may interact with medications that are substrates of CYP3A4 as well as medications that inhibit or induce CYP3A4 activity. Drug-drug interactions should be considered prior to starting therapy with Tegazel Tablet 6 mg.
Tegazel Tablet 6 mg may be taken with or without food. The absorption of Tegazel Tablet 6 mg is not known to be affected by food.
Tegazel Tablet 6 mg is not recommended for use during pregnancy. Animal studies have shown an increased risk of fetal abnormalities, but there are no adequate and well-controlled studies of Tegazel Tablet 6 mg use in pregnant women.
Tegazel Tablet 6 mg is not recommended for use during breastfeeding. It is not known whether Tegazel Tablet 6 mg is excreted in human milk.
In the event of an overdose, the patient should be monitored closely for any signs of adverse reactions and appropriate medical intervention should be administered. There is no specific antidote for an acute overdose of Tegazel Tablet 6 mg.
Tegazel Tablet 6 mg is contraindicated in patients with a known hypersensitivity to Tegazel Tablet 6 mg or any of its components. Additionally, Tegazel Tablet 6 mg should not be used in patients with known or suspected gastrointestinal obstruction, history of GI perforation, and/or severe diarrhea.
Tegazel Tablet 6 mg should be taken orally, with or without food, every day at the same time. The tablets should be swallowed whole with fluids. For the symptomatic treatment of irritable bowel syndrome with constipation (IBS-C), the recommended dose is 6 mg once daily. For the treatment of chronic constipation, the recommended dose is 12 mg once daily.
Tegazel Tablet 6 mg should be stored at room temperature away from moisture, heat, and light.
Tegazel Tablet 6 mg has a volume of distribution of approximately 1.4 L/kg.
The elimination half-life of Tegazel Tablet 6 mg is approximately 11 hours.
The clearance of Tegazel Tablet 6 mg is approximately 0.25 L/h/kg.
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Dr. Md. Rezwan Rehan
Cardiology (Heart Diseases, Hypertension & Rheumatic Fever) Specialist