Hafrokin Injection (Fursultiamine Hydrochloride)
Fursultiamine Hydrochloride 5.46mg
Injections · Prescription medication
Hawon Pharmaceutical Co., Ltd.
MFDS item code 200713063 · Notified 2007.12.06
Improvement of symptoms related to Vitamin B1 deficiency and metabolic disorders.
This medication is used for the prevention and treatment of Vitamin B1 deficiency. It is also used as a supplement in cases where the demand for Vitamin B1 increases and adequate intake through diet is difficult, such as in cases of wasting diseases, hyperthyroidism, pregnancy or breastfeeding, and intense physical labor. It is effective for certain neurological and heart-related diseases such as Wernicke's encephalopathy and beriberi heart disease. It is also used for various symptoms associated with suspected Vitamin B1 deficiency or metabolic disorders, including neuralgia, myalgia, arthralgia, peripheral neuritis, myocardial metabolic disorders, gastrointestinal motility disorders, postoperative bowel paralysis; however, care should be taken to avoid long-term use without purpose. This medication helps improve Vitamin B1 deficiency and treat related symptoms.
As fursultiamine, typically administered 5 – 100 mg under the skin, intramuscularly, or intravenously per day for adults. Adjust according to symptoms.
This medication is in an ampoule form, and when opening the ampoule, glass fragments may get mixed in. Therefore, care should be taken when cutting the ampoule to avoid glass pieces entering. Extra caution is needed when using in children and the elderly. Patients who have had allergic reactions to the ingredients in this medication should not use it. Patients with a history of drug allergies should be cautious when using this medication. Serious adverse reactions like shock may occur rarely when using this medication, so if symptoms such as low blood pressure, chest pain, or shortness of breath appear, discontinue use immediately and seek appropriate treatment. Additionally, if symptoms of skin allergy such as rash appear, use of this medication should be stopped. Occasional gastrointestinal issues such as nausea, vomiting, mouth inflammation, diarrhea, and headaches, as well as symptoms of frequent urination, may occur. When administering this medication intravenously, it is important to inject slowly to minimize vascular pain. To prevent bacterial contamination, any remaining medication should not be reused after opening. When opening the ampoule, it should be oriented with the marked side up and the opposite side pressed gently for safe cutting, and the upper part of the ampoule should be cleaned with an alcohol swab to avoid contamination. This medication should be stored out of reach of children, and transferring it to another container can lead to accidents or deterioration in drug quality.
Not everyone experiences these, and they can vary from person to person.
This medication is sensitive to light, so it should be stored in a container that does not allow light in. Additionally, it is important to maintain a storage temperature between 1 to 30 degrees Celsius. This helps preserve the medication's efficacy.
A clear liquid that is colorless to pale yellow contained in a transparent brown glass ampoule.
1 ampoule (10mL) x 10 ampoules
Even with the same ingredient, strength, dosage form and how it is taken can differ.
Fursultiamine Hydrochloride 5.46mg
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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.