Emistat FT 4mg Tablet contains Ondansetron, which belongs to a group of medicines called Anti-emetics. It is used to treat and prevent nausea and vomiting induced by chemotherapy or radiotherapy. Emistat FT 4mg Tablet is also used after surgeries (operations) to prevent nausea and vomiting.
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Emistat FT 4mg Tablet is a type of anti-emetic medication that is mainly used to prevent vomiting and nausea, which can occur after undergoing chemotherapy, radiation treatment, or surgery. Nausea is a feeling of discomfort that may cause a person to want to vomit, whereas vomiting is the body's natural response to expel the contents of the stomach forcefully.
The active ingredient in Emistat FT 4mg Tablet is Ondanestron, which works by blocking the action of serotonin, a chemical in the body responsible for causing nausea and vomiting. By doing so, Emistat FT 4mg Tablet can help prevent the unpleasant sensation of nausea and vomiting associated with conditions such as motion sickness, pregnancy, surgery, or cancer chemotherapy.
It's essential to take Emistat FT 4mg Tablet as directed by a healthcare provider.
Avoid consuming alcohol while taking Emistat FT 4mg Tablet as this medicine can interact with alcohol and may worsen the side effects.
Emistat FT 4mg Tablet could be used during pregnancy after consulting a doctor.
Emistat FT 4mg Tablet could be used during breastfeeding after consulting a doctor.
Emistat FT 4 does not usually affect your ability to drive.
The use of Emistat FT 4mg Tablet is safe in patients dealing with kidney disorders. No dose adjustment is required.
The use of Emistat FT 4mg Tablet in people with liver disorders is permitted if recommended by a doctor. Patients with serious liver issues, on the other hand, should take a modest dose of Emistat FT 4mg Tablet as much as feasible. In the case of liver problems, do not exceed 8 mg of Emistat FT Tablet per day.
The serotonin 5-HT3 receptor antagonist (particular chemical receptor) Emistat FT 4 acts by inhibiting serotonin receptors in the CTZ chemoreceptor trigger zone. (zone in the brain that is responsible for causing nausea and vomiting).
Ondansetron could be a serotonin subtype 3 (5-HT3) receptor opponent indicated:
Ondansetron has the potential to be a potent and highly selective 5HT3 receptor antagonist. Its precise mechanism of action in the regulation of nausea and heaving is unknown. By activating vagal afferents via 5HT3 receptors, chemotherapeutic treatments, and radiation might elicit 5HT release inside the small intestinal tract, resulting in a spitting reflex. Ondansetron prevents the initiation of this response. The activation of vagal afferents may also result in a release of 5HT inside the zone postrema, which is located on the floor of the fourth ventricle, which may further promote emesis via a central component. As a result, the effect of ondansetron in the treatment of disease and vomiting caused by cytotoxic chemotherapy and radiation is most likely related to the antagonism of 5HT3 receptors on neurons present both in the peripheral and central nervous systems. The mechanisms of action in postoperative nausea and heaving are unknown, however, there may be shared pathways with cytotoxic-induced nausea and heaving.
These are the recommended dosages for Ondace for different types of nausea and vomiting:
For Chemotherapy-induced nausea and vomiting:
For Radiotherapy-induced nausea and vomiting:
For Postoperative nausea and vomiting:
Contraindicated in patients known to have extreme touchiness to the medication or any of its components. Concomitant utilization of apomorphine.
Pregnancy Category B. Ondansetron is excreted within the breast milk of rats. It isn't known whether ondansetron is excreted in the human drain. Since numerous drugs are excreted in the human brain, caution ought to be worked out when ondansetron is managed by a nursing lady.
Store at a temperature not surpassing 30ºC in a dry put. Secure from light and dampness.
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