Galonik Injection (Fursultiamine Hydrochloride)
Fursultiamine Hydrochloride 5.46mg
Prescription medication
Kyungnam Pharmaceuticals Co., Ltd.
MFDS item code 200807341 · Notified 2008.07.02
Prevention and treatment of neurological pain, cardiac disorders, and other conditions related to vitamin B1 deficiency and metabolic disorders.
This medication is used to prevent and treat vitamin B1 deficiency. It is also used as a supplement when the need for vitamin B1 increases and is not sufficiently met by diet, such as in cases of hyperthyroidism, during pregnancy and breastfeeding, and with strenuous physical labor. It is effective for neurological and cardiac disorders such as Wernicke's encephalopathy and beriberi heart disease. Additionally, it helps with symptoms suspected to be due to vitamin B1 deficiency or metabolic disorders, such as neuralgia, myalgia, and peripheral neuropathy. However, it is important not to use this medication aimlessly for more than one month if it is not related to vitamin B1 deficiency. Overall, this drug is used to improve symptoms associated with vitamin B1 deficiency and its related conditions.
As fursultiamine, the usual adult dosage is 5 to 100 mg administered subcutaneously, intramuscularly, or intravenously per day. Adjust dosage appropriately based on symptoms.
This medication is in a glass ampoule form, so care must be taken when opening to prevent glass fragments from mixing in. Special caution is needed when used in children or the elderly. Do not use this medication in patients who have had allergic reactions to it or any of its ingredients. It should be administered cautiously to patients with a history of allergic reactions to medications. Serious shock may rarely occur with the use of this medication, therefore if symptoms such as hypotension, chest pain, or shortness of breath appear, immediately discontinue administration and seek appropriate treatment. Additionally, if allergic symptoms such as skin rashes occur, administration should be stopped, and side effects such as nausea, vomiting, stomatitis, diarrhea, headache, and frequent urination may occur. When administering intravenously, this medication should be infused slowly to reduce vascular pain. To prevent bacterial contamination, any remaining solution should not be reused. When breaking the ampoule, position the marked area on the top and apply force downward to cleanly separate, and the upper part of the ampoule should be cleaned with alcohol cotton to prevent contamination. This medication should be stored out of the reach of children, and transferring it to another container should be avoided as it may cause deterioration in quality or accidents.
Not everyone experiences these, and they can vary from person to person.
This medication is sensitive to light and should be stored in a container that does not allow light to enter. It should also be stored at room temperature between 1 to 30 degrees Celsius to maintain the efficacy of the drug.
A colorless, odorless liquid with a slight bitterness, contained in a brown ampoule as a clear liquid.
10 milliliters/ampoule [(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.