Fluorosulfide Hepa Injection
L-Proline 6000mg · L-Histidine 1875mg +13 more
Injections · Prescription medication · Combination
HK Inno.N Co., Ltd.
MFDS item code 199301540 · Notified 1993.05.31
Improvement of encephalopathy due to acute and chronic liver dysfunction and amino acid supply effect.
This medication is used to improve the symptoms of encephalopathy caused by acute and chronic liver dysfunction and to supplement amino acids needed by patients with liver dysfunction. This helps in the recovery of liver function and improvement of neurological status.
As a total amino acid, infuse intravenously at a maximum dosage of 1-1.5 g per kg of body weight daily. An infusion rate of a total amino acid concentration of approximately 10 g over 60 minutes is desirable; it is principle to infuse at a rate of 30-40 drops per minute.
Dosage and infusion rate for children must be adjusted appropriately.
This medicine must be used according to a doctor's instructions. It is safe not to use this medication in patients with severe renal impairment or hyperazotemia. Additionally, it should not be administered to patients with problems in amino acid metabolism, as well as those with metabolic diseases that impair nitrogen utilization or patients with severe heart failure or pulmonary edema. Caution is necessary for patients with very low or absent urine volume, high sodium and chloride levels, and those with atrioventricular block or severe myasthenia gravis. Administration is not recommended in patients with excessive water supply. The medication should be used cautiously in patients with severe acidosis, heart failure, edema due to sodium retention, hyperkalemia, and those with reduced kidney function. Rarely, hypersensitivity reactions like skin rashes may occur, and administration should be stopped immediately if symptoms arise. Gastrointestinal symptoms like nausea or vomiting, chest discomfort, or rapid heart rate may occur. Rapid administration of large volumes may lead to acidosis, so caution is required. Symptoms such as chills, fever, headache, and respiratory distress have also been reported. If magnesium is included, peripheral blood vessels may dilate, so caution is needed. Various metabolic complications such as metabolic acidosis, hypophosphatemia, hyperglycemia, and electrolyte imbalances may occur. Patients with severely impaired liver or kidney function may experience elevated waste levels in the blood, requiring close monitoring of their condition. When administering large doses of this medication or using it with other electrolyte-containing fluids, particular attention should be paid to electrolyte balance. Overdosage may cause metabolic alkalosis, so the dosage should be carefully adjusted based on the constituents included. Diabetic patients should regularly check their blood glucose levels during administration. Patients with kidney, lung, or heart diseases need to be cautious to avoid excessive body fluid increases. This medication can interact with other medications, especially when used with tetracycline antibiotics, calcium salts, or vitamin B1, hence consultation with a professional is necessary. Its safety has not been established in pregnant women, so it should only be used when the benefits of treatment outweigh the risks. For children, the concentration should be lowered due to possible immature liver function, and blood ammonia levels should be regularly checked. Elderly individuals may have decreased bodily functions, so administration rates should be slow, and dosages should be adjusted. This medication contains electrolytes, so electrolyte balance must always be checked during administration, and administration should be done slowly to avoid side effects. Before use, ensure the solution is clear and transparent, and do not use if it is discolored or abnormal.
Hives, severe swelling (edema), chest tightness, difficulty breathing, pallor, severe allergic reactions, severe rashes, blisters, skin peeling, pain in mucous membranes of the mouth/eyes, severe skin reactions, difficulty breathing, asthma attacks, cough accompanied by fever, respiratory abnormalities, jaundice, severe lethargy, liver dysfunction (jaundice), significant edema or urination abnormalities, shortness of breath or difficulty breathing, respiratory arrest, shock.
Not everyone experiences these, and they can vary from person to person.
This medication should be stored in a sealed container to prevent air or moisture infiltration, and it is advisable to keep it at room temperature away from direct sunlight. By maintaining appropriate storage methods, the efficacy of the medication can be preserved for a long time.
A transparent, colorless or pale yellow transparent injectable solution filled in a colorless, transparent plastic container.
100, 250 milliliters
Even with the same ingredient, strength, dosage form and how it is taken can differ.
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Injections · Prescription medication · Combination
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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.