Phuther sulthamine injection (Phutherstiamine hydrochloride)
Fursultiamine Hydrochloride 5.46mg
Prescription medication
Nokshimp Wellbeing Co., Ltd.
MFDS item code 200704485 · Notified 2007.04.18
Prevention and treatment effects for vitamin B1 deficiency and metabolic disorders (neuralgia, myocardial metabolic disorders, etc.)
This medication is used to prevent and treat several problems arising from vitamin B1 deficiency. For example, it prevents vitamin B1 deficiency disease and aids vitamin B1 supplementation when dietary intake is insufficient, during pregnancy or breastfeeding, or in cases of intense physical labor. It is also effective in treating serious conditions such as Wernicke's encephalopathy and beriberi heart disease. It is used to improve various symptoms associated with vitamin B1 deficiency or metabolic disorders, such as neuralgia, myalgia, peripheral neuropathy, myocardial metabolic disorders, and gastrointestinal motility dysfunction. However, if no effect is observed after one month, indiscriminate use should be avoided. Overall, this medication is used to improve vitamin B1 deficiency and related symptoms.
As Phutherstiamine, the usual dosage for adults is 5 to 100 mg administered subcutaneously, intramuscularly, or intravenously per day. Adjust according to the symptoms.
This medication is in a glass ampule injection format, so care should be taken when opening the injection container to avoid glass fragments. Extra caution is particularly needed when administering to children or the elderly. It should not be used in patients who have previously had allergic reactions to this medication or its components. Care is particularly necessary before administering to patients with a history of allergic reactions. Rarely, serious side effects such as shock can occur, so if symptoms such as a decrease in blood pressure, chest pain, or difficulty breathing occur during administration, the injection should be stopped immediately, and appropriate treatment should be provided. Additionally, side effects such as rash, nausea, vomiting, oral inflammation, diarrhea, headache, and frequent urination can occur, and it is advisable to stop administration if these symptoms develop. Pain may occur in the blood vessel during injection, so it should be administered as slowly as possible. When using the injection solution, leftover medication should not be reused to prevent bacterial contamination. Care should be taken to wipe the ampule with clean ethanol cotton to avoid contamination when cutting, ensuring that the marked part of the ampule faces upwards and lightly pressing the opposite side to cut. This medication should be stored in a secure place out of reach of children, and should not be transferred to another container as this may affect quality or cause accidents; it must be stored in the original container.
Hypotension, chest pain, difficulty breathing → shock symptoms, immediate cessation of administration and treatment required
Not everyone experiences these, and they can vary from person to person.
This medication should be stored in a tightly sealed container that blocks light, and the storage temperature should be kept between 1 and 30 degrees Celsius at room temperature. Storing it this way helps maintain the effectiveness and safety of the medication.
A brown ampule containing a colorless transparent liquid
10 ampules/box [(10mL/ampule)x10], 50 ampules/box [(10mL/ampule)x50]
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.