Medication info

Hamonilan Liquid

Prescription medicationSuspension경구
Ingredient · strength
Vegetable Protein›0.65g / 100mLReduced-Lactose Protein›4.5g / 100mLRefined Soyabean Oil›2.8g / 100mLWhey Powder›1.2g / 100mLSucrose›4.05g / 100mLMaltodextrin›7.9g / 100mLCorn Starch›0.7g / 100mLSoybean Hull Dietary Fiber Powder›1.35g / 100mLSynthetic Retinol Acetate Concentrate Powder›0.32mg / 100mLThiamine Hydrochloride›1.118mg / 100mLRiboflavin›0.24mg / 100mLPyridoxine Hydrochloride›0.486mg / 100mLAscorbic Acid›20mg / 100mLTocopherol Acetate Concentrate Powder›3.732mg / 100mLNicotinamide›4mg / 100mLFolic Acid›0.09mg / 100mLCalcium Pantothenate›3.2mg / 100mLCyanocobalamin Powder›0.4mg / 100mLBiotin›0.02mg / 100mLSodium Chloride›127mg / 100mLPotassium Citrate Hydrate›157mg / 100mLCalcium Citrate Hydrate›85.6mg / 100mLLight Magnesium Carbonate›24.3mg / 100mLFerrous Sulfate Hydrate›2.44mg / 100mL
Manufacturer / importer
비브라운코리아(주)
Appearance
The product is a brownish suspension with a unique odor and a sweet taste.
Packaging
200 milliliters / 500 milliliters
Approval status
Active

MFDS item code 201007457 · Approved 2010.12.09 · Insurance code 667400852,667400853

Summary

Main use
Nutritional maintenance and improvement through enteral nutrition supply
Who takes it
Adults
Adult dose
The standard adult dosage is 1,500-2,000 mL (1,500-2,000 Kcal) per day, administered continuously or divided into several doses through a nasal tube, gastrostomy, or jejunostomy into the stomach, duodenum, or jejunum. The infusion rate should be 100 mL/hour. If oral intake is possible, it may be administered once daily or divided into several oral doses. At the start of administration, it is usually diluted with water at 400 mL (400 Kcal) per day.

Ingredients

Importer
비브라운코리아(주)

Efficacy & effects

Nutritional maintenance and improvement through enteral nutrition supply

View approved original text

This medication is used to maintain the nutritional status of patients after surgery. It especially helps provide nutrition through the enteral route when patients have difficulty consuming food orally. It supports patients in obtaining adequate nutrition, promoting recovery. It is effective in preventing nutritional imbalance or malnutrition. Therefore, this medication is used for the nutritional supply of patients who are unable to take in nourishment orally.

How to take

Adult dose

The standard adult dosage is 1,500-2,000 mL (1,500-2,000 Kcal) per day, administered continuously or divided into several doses through a nasal tube, gastrostomy, or jejunostomy into the stomach, duodenum, or jejunum. The infusion rate should be 100 mL/hour. If oral intake is possible, it may be administered once daily or divided into several oral doses. At the start of administration, it is usually diluted with water at 400 mL (400 Kcal) per day.

Precautions

This drug should be strictly limited in the case of women in the first three months of pregnancy or women with the possibility of becoming pregnant when administering more than 5,000 IU of vitamin A daily, as it poses a risk of congenital malformations in the fetus. Individuals with allergies to the ingredients in this medication or who are sensitive to milk should not use it due to the presence of milk protein, which can cause severe allergic reactions. Patients with gastrointestinal issues, intestinal obstruction, congenital amino acid metabolism disorders, loss of bowel function, acute inflammatory bowel disease, preoperative conditions for colon cancer, and hepatic coma should not use this medication as it may worsen their symptoms. Patients with reduced bowel function, decreased kidney function, metabolic abnormalities of carbohydrates, acute pancreatitis, and unstable fluid balance must be cautious when administered this treatment, adjusting doses and infusion rates as necessary. This medication may cause gastrointestinal side effects such as diarrhea, abdominal pain, and abdominal bloating. In severe cases, allergic reactions or anaphylactic shock may occur, requiring immediate discontinuation of the treatment and appropriate medical intervention. When administered to postoperative patients, it is important to monitor gastrointestinal motility and adjust dosage and infusion rates accordingly. Once sufficient nutritional intake is possible orally, it is advisable to quickly transition to oral feeding. Long-term use may lead to a deficiency of vitamins, electrolytes, or trace elements, requiring supplementation as necessary, and should not be used in patients requiring special nutritional formulations, such as those in hepatic coma. Pregnant or breastfeeding women should avoid excessive intake of vitamin A, particularly limiting to less than 5,000 IU during early pregnancy. Safety for children has not been established as there is no experience in use; caution is needed. Elderly patients may more easily experience gastrointestinal symptoms, and adjustments such as reducing dosage or discontinuation should be taken if symptoms arise. This medication should not be administered intravenously. When given enterally, the residual presence of gastric contents should be checked intermittently during administration, and the feeding tube should be cleaned afterward. Before use, shake well. The infusion rate and concentration should be gradually increased while monitoring for side effects, lowering or stopping if they occur. Do not use if the container is damaged, and be cautious of products containing DEHP, as it may leach from nutrient sets or feeding tubes; using products without DEHP is advisable. Keep this medication out of reach of children, and avoid transferring it to other containers, which could affect quality. Use immediately after opening and take care to avoid degradation during storage.

Side effects and when to seek care immediately

Serious side effects

  • Shock
  • anaphylactic symptoms
  • hypotension
  • disturbances in consciousness
  • difficulty breathing
  • cyanosis
  • chest discomfort

Mild side effects

  • Diarrhea
  • abdominal pain
  • abdominal bloating
  • vomiting
  • nausea
  • thirst
  • heartburn
  • elevated potassium
  • increased blood urea nitrogen
  • rash
Show 9 more
  • blistering dermatitis
  • hypotension
  • disturbances in consciousness
  • cyanosis
  • nausea
  • chest tightness
  • flushing
  • itching
  • sweating

Not everyone experiences these, and they can vary from person to person.

Storage

This medication is packaged in a light-blocking sealed container and is available in two volumes: 200mL and 500mL. It should be stored at room temperature between 1°C and 30°C, and it is important to keep it protected from light and air by storing it in a light-proof container.

Appearance and packaging

Appearance

The product is a brownish suspension with a unique odor and a sweet taste.

Package unit

200 milliliters / 500 milliliters

Questions about this medicine

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For anything that needs medical judgment, consult a doctor or pharmacist.

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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.