Hanaramseteu Vial Injection 0.3 mg (Ramosetron Hydrochloride)
Ramosetron Hydrochloride 0.3mg
Injections · Prescription medication
Hana Pharmaceutical Co., Ltd.
MFDS item code 202501338 · Approved 2025.05.29
Prevention of nausea and vomiting associated with chemotherapy and postoperative conditions.
This medication is used to prevent nausea and vomiting that may occur with the administration of chemotherapeutic agents such as cisplatin, and also to prevent nausea and vomiting after surgery.
Adults: Administer 0.3 mg of Ramosetron Hydrochloride intravenously once daily. If the effect is insufficient, the same dose may be administered additionally, but do not exceed 0.6 mg in a single day. Adjustments should be made according to symptoms.
This medication should not be used in patients who have had an allergic reaction to this drug or any of its components. Exercise caution when administering to patients who are taking other serotonergic medications, such as selective serotonin reuptake inhibitors (SSRIs) or serotonin-norepinephrine reuptake inhibitors (SNRIs), as this may lead to a serious side effect known as serotonin syndrome, and careful monitoring is required. Serious allergic reactions such as shock or anaphylaxis may occur when using this medication; if unusual symptoms arise, administration should be stopped immediately and appropriate treatment should be sought. Additionally, seizures similar to epilepsy may rarely occur, so if neurological symptoms arise, consult medical personnel immediately. Side effects such as headache, diarrhea, constipation, and liver function abnormalities have been reported; if these symptoms persist or worsen, consult a doctor. Safety during pregnancy has not been sufficiently established, so it should be used cautiously under a doctor's supervision only when necessary, and breastfeeding should be discontinued during use. Safety in children has not been established; thus, special care is needed when administering to children. Elderly patients may have decreased body function, so careful observation is necessary during administration, and immediate action should be taken if side effects occur. This medication may alter compatibility when mixed with certain injection solutions; therefore, caution should be exercised during preparation, and mixing with some injection solutions should be avoided. Finally, animal studies have reported potential risks to the fetus, so women of childbearing potential should consider this when using the drug.
Shock, anaphylaxis-like symptoms (chest tightness, difficulty breathing, asthma, facial flushing, redness, itching, cyanosis, hypotension), seizures similar to epilepsy.
Not everyone experiences these, and they can vary from person to person.
This medication is sensitive to light and should be stored in a dark place, protected from light. It should also be kept in a sealed container to avoid contact with air, and it is important to maintain a storage temperature between 1 to 30 degrees Celsius.
A colorless, clear solution in a brown vial for injection.
5 vials/box [2 milliliters/vial]
Even with the same ingredient, strength, dosage form and how it is taken can differ.
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Even with the same ingredient, the dose and directions can differ by strength and dosage form. Talk to a doctor or pharmacist before switching from a medication you are already taking.
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For anything that needs medical judgment, consult a doctor or pharmacist.
This drug information is based on data provided by the Korea Ministry of Food and Drug Safety.
Consult a doctor or pharmacist for accurate dosage, administration, and usage instructions.