Medication info

Hepamelz Injection (L-Aspartic Acid-L-Ornithine)

Prescription medication정맥
Ingredient · strength
L-Ornithine-L-Aspartate›500mg / 1 ampoule
Manufacturer / importer
한화제약(주)
Appearance
Brown glass ampoules containing a colorless and transparent liquid
Packaging
10 ampoules/box [(5 milliliters/ampoule)]
Approval status
Active

MFDS item code 198300707 · Notified 1983.02.14 · Insurance code 651600921

Summary

Main use
Adjunctive therapy for severe liver diseases (hepatitis, cirrhosis, etc.)
Who receives it
Adults
Adult administration
For patients with severe liver disease, administer L-Aspartic Acid-L-Ornithine intravenously at a dose of 2g (4 ampoules) daily for 7 days.

Ingredients

Manufacturer
한화제약(주)

Efficacy & effects

Adjunctive therapy for severe liver diseases (hepatitis, cirrhosis, etc.)

  • Severe liver diseases
  • hepatitis
  • sequelae of hepatitis
  • cirrhosis
View approved original text

This medication is used as an adjunctive treatment for severe liver diseases. It is particularly beneficial for serious liver conditions such as hepatitis, sequelae of hepatitis, and cirrhosis. It aids in the recovery of liver function and supports the detoxification process to improve liver status.

How it is given

Adult administration

For patients with severe liver disease, administer L-Aspartic Acid-L-Ornithine intravenously at a dose of 2g (4 ampoules) daily for 7 days.

Precautions

This medication is provided in a glass ampoule form, so care must be taken to avoid glass fragments when cutting the container. Particularly cautious administration is required for children and the elderly. This medication should not be used in patients with certain conditions. For example, it should be avoided in patients with lactic acidosis, methanol poisoning, fructose-sorbitol intolerance, fructose-1,6-diphosphatase deficiency, and severe renal impairment. As this medication contains sodium pyrosulfite, it may cause allergic reactions or asthma attacks in individuals sensitive to sulfites, especially asthma patients. Administration of this medication may sometimes lead to sensations of warmth at the back of the head, nausea, gastric discomfort, and vomiting. During high-dose administration, blood or urine urea levels should be checked for abnormality. If liver function is poor, the infusion rate should be adjusted to reduce discomfort or vomiting. This medication should be administered slowly intravenously, as rapid administration may increase the risk of side effects.

Side effects and when to seek care immediately

Serious side effects

Asthma attack, severe allergic reactions such as sulfite anaphylaxis

Mild side effects

  • Warm sensation in the occiput
  • nausea
  • gastric discomfort
  • vomiting

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

Storage

This medication should be stored in a sealed container and kept at room temperature between 1 to 30 degrees Celsius. Storing it this way will ensure the medication's effectiveness is safely maintained.

Appearance and packaging

Appearance

Brown glass ampoules containing a colorless and transparent liquid

Package unit

10 ampoules/box [(5 milliliters/ampoule)]

Same-ingredient medicines

Even with the same ingredient, strength, dosage form and how it is taken can differ.

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.

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.