Cheil Hypervitamin B1 (Fursultiamine Hydrochloride)
Fursultiamine Hydrochloride 5.46mg
Prescription medication
Cheil Pharmaceutical Co., Ltd.
MFDS item code 201605945 · Notified 2016.10.07
Prevention and treatment effects for vitamin B1 deficiency and metabolic disorder-related neuralgia, cardiac disorders, etc.
This medication is used for the prevention and treatment of various symptoms and diseases caused by vitamin B1 deficiency. It is particularly helpful for neurological symptoms such as neuralgia, myalgia, and peripheral neuropathy that can occur when vitamin B1 is insufficient, as well as serious diseases such as beriberi heart disorder and Wernicke's encephalopathy. It is also used to supplement the increased demand for vitamin B1 due to hyperthyroidism, pregnancy, breastfeeding, and intense physical labor. However, it is effective only in cases where vitamin B1 deficiency or metabolic disorders are suspected, and it is important not to use it for long periods without purpose. This medication is useful for improving symptoms caused by vitamin B1 deficiency and for maintaining health.
As Fursultiamine, typically, adults are injected subcutaneously, intramuscularly, or intravenously with 5 to 100 mg daily. Dosage should be adjusted appropriately according to the symptoms.
This medication must be carefully cut when using it as an injection. If glass fragments are mixed in, adverse reactions may occur, so special caution is needed when used in children and the elderly. Patients with a history of allergic reactions to this medication or its components should not use it. Caution should be exercised when administering it to patients with a history of allergies, and if abnormal symptoms appear, administration should be stopped immediately. Rarely, serious reactions such as shock may occur when using this medication. If symptoms such as falling blood pressure, chest pain, or shortness of breath appear, administration should be stopped immediately, and appropriate treatment should be received. Additionally, rare hypersensitivity reactions such as skin rashes may occur, and gastrointestinal symptoms such as nausea, vomiting, inflammation of the mouth, diarrhea, as well as headaches and frequent urination may develop. When administered intravenously, there may be pain in the veins, so the injection rate should be adjusted slowly. The remaining solution should be discarded after use to prevent contamination, and care should be taken to clean the ampoule before cutting to avoid foreign substances. Lastly, this medication should be stored in a safe place out of the reach of children, and transferring it to another container may increase the risk of accidents and decrease the quality of the medication, so it must be stored in the original container.
Not everyone experiences these, and they can vary from person to person.
This medication is sensitive to light and should be stored in an opaque container. Additionally, to maintain the medication's effectiveness, it should be stored at room temperature, between 1 and 30 degrees Celsius. It is advisable to avoid excessively hot or cold places.
This medication is a colorless, odorless liquid with a slight bitterness, contained in brown ampoules as a transparent liquid.
10 mL/ampoule x 10 ampoules
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.