Furotimine Injection (Fursultiamine Hydrochloride)
Fursultiamine Hydrochloride 5.46mg
Prescription medication
Daehan Pharmaceutical Co., Ltd.
MFDS item code 200713093 · Notified 2007.12.06
Prevention and treatment of vitamin B1 deficiency and neuralgia
This injection is used for the prevention and treatment of vitamin B1 deficiency. It is administered in cases of inadequate intake of vitamin B1, such as in wasting diseases, hyperthyroidism, during pregnancy and breastfeeding, and during intense physical labor for supplementation purposes. It is also beneficial in the treatment of neurological and cardiac-related diseases such as Wernicke's encephalopathy and beriberi cardiac disorder. Additionally, it is used in cases associated with vitamin B1 deficiency or metabolic disorders, such as neuralgia, myalgia, arthralgia, peripheral neuritis and paralysis, cardiac metabolic disorders, and gastrointestinal motility disorders like constipation. However, it is important not to administer it for long periods in states unrelated to vitamin B1 deficiency. This injection is effective for the treatment of vitamin B1 deficiency and related diseases.
As fursultiamine, the typical dosage for adults is 5 to 100 mg administered subcutaneously, intramuscularly, or intravenously per day. It should be adjusted appropriately based on symptoms.
This medication is administered intravenously, and care should be taken as glass fragments may enter when opening the ampoule. Extra caution is needed when it is used in children and the elderly. It should not be used in individuals who are allergic to this drug or any of its components. Caution should be exercised when administering it to patients with a history of drug allergies. Rarely, severe side effects like shock may occur, so if symptoms such as hypotension, chest pain, or respiratory distress appear during administration, it should be stopped immediately and appropriate treatment should be provided. If allergic reactions such as rashes occur, administration should be discontinued, and side effects like nausea, vomiting, stomatitis, diarrhea, headache, frequent urination may also occur, though rarely. To reduce vascular pain during intravenous injection, it is advisable to administer it slowly, and the remaining solution should not be reused to prevent bacterial contamination. When opening the ampoule, it should be oriented with the marked side facing up, and the opposite side should be lightly pressed to ensure a clean break. The upper part of the ampoule should be cleaned with an alcohol swab to prevent foreign contamination. This medication should be stored out of reach of children, and transferring it to another container should be avoided as it may lead to quality deterioration or accident risks.
Not everyone experiences these, and they can vary from person to person.
This drug is sensitive to light, so it should be stored in a container that does not allow light to enter. Additionally, it is important to maintain a temperature between 1°C to 30°C when storing the drug. This helps preserve the efficacy and safety of the medication for a longer period.
Brown ampoule containing a colorless and transparent solution
10mL 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.