Europe — EMA
Granissetrom Baxter
Granissetrom Baxter is a Granisetron intravenous antiemetic for chemotherapy‑ and postoperative‑induced nausea and vomiting. Learn uses, side effects, and precautions.
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What is Granisetron?
Granissetrom Baxter is a prescription medication that contains the active ingredient granisetron, supplied as an intravenous solution (strength not specified). It belongs to the 5‑HT3 receptor antagonist class and is marketed in the European Union. Granisetron works by blocking serotonin receptors in the chemoreceptor trigger zone and gastrointestinal tract, helping to prevent nausea and vomiting associated with chemotherapy and surgery or other emetogenic treatments in patients.
What is Granisetron used for?
Granissetrom Baxter is indicated for the prevention and treatment of nausea and vomiting in several clinical settings.
- Chemotherapy‑induced nausea and vomiting (CINV) in adult patients receiving moderately to highly emetogenic chemotherapy. - Postoperative nausea and vomiting (PONV) following general anesthesia and surgical procedures. - Nausea and vomiting associated with radiation therapy when administered as part of a multimodal antiemetic regimen. - Prevention of emesis in patients receiving highly emetogenic cancer treatments where other antiemetics are insufficient.
What are the side effects of Granisetron?
The safety profile of Granisetron intravenous includes both frequent mild reactions and rare but potentially serious events.
Common: - Headache - Constipation - Fatigue - Dizziness
Serious: - Severe allergic reaction (anaphylaxis) - Cardiac arrhythmias, including QT interval prolongation
What precautions apply to Granisetron?
Before initiating Granissetrom Baxter, clinicians should evaluate patient-specific factors and monitor for known risks.
- Assess for known hypersensitivity to granisetron or other 5‑HT3 antagonists. - Use cautiously in patients with a history of cardiac conduction disorders or prolonged QT interval. - Evaluate renal and hepatic function, as dose adjustments may be required in severe impairment. - Consider potential pregnancy or lactation status; safety data are limited. - Monitor for signs of constipation or ileus, especially in postoperative patients. - Avoid concurrent use with other serotonergic agents that may increase the risk of serotonin syndrome.
What does Granisetron interact with?
Granisetron may interact with other medications, influencing its efficacy or safety profile.
Avoid: - Concomitant use with other 5‑HT3 receptor antagonists, which can increase the risk of cardiac toxicity. - Co‑administration with drugs that markedly prolong the QT interval (e.g., certain antiarrhythmics, antipsychotics).
Use with caution: - Antidepressants or other serotonergic agents, due to a theoretical risk of serotonin syndrome. - CYP3A4 inhibitors or inducers, which may alter granisetron plasma concentrations. - Opioid analgesics, as they can also cause constipation and may compound gastrointestinal effects.
Frequently asked questions
What is Granissetrom Baxter and how does it work?+
How is Granisetron administered intravenously?+
In which patients is Granisetron intravenous most commonly used?+
What are the common side effects of Granisetron IV?+
What serious adverse reactions should be reported with Granisetron IV?+
Can Granisetron be used during pregnancy or breastfeeding?+
How should Granisetron be stored before use?+
Are there any drug interactions to avoid with Granisetron IV?+
What cardiac monitoring is recommended when using Granisetron?+
How does Granisetron compare to other antiemetics for chemotherapy?+
What should I do if I miss a scheduled Granisetron IV dose?+
Is Granisetron effective for radiation‑induced nausea?+
Product details
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