Medication info
Carnitine Tablets (L-Carnitine)

Carnitine Tablets (L-Carnitine)

OTC medicationTabletOral
Ingredient · strength
L-Carnitine›330mg / 1 tablet
Manufacturer / importer
AlliCo Pharmaceutical Co., Ltd.
Appearance
White round film-coated tablets
Packaging
90 tablets (10 tablets/PTP × 9)
Approval status
Active

MFDS item code 201605433 · Notified 2016.09.05

Summary

Main use
Treatment of carnitine deficiency and myocardial metabolic disorders due to ischemic heart disease
Who takes it
Adults
Adult dose
Adults: Administer 2-3 g of L-carnitine per day orally in 2-3 divided doses. The dose may be adjusted as appropriate according to age and symptoms.

Ingredients

Manufacturer
AlliCo Pharmaceutical Co., Ltd.

Efficacy & effects

Treatment of carnitine deficiency and myocardial metabolic disorders due to ischemic heart disease

  • Carnitine deficiency
  • myocardial metabolic disorders due to ischemic heart disease
  • angina pectoris
  • acute myocardial infarction
View approved original text

This medication is used in the treatment of primary and secondary carnitine deficiency and myocardial metabolic disorders due to ischemic heart disease, namely angina and acute myocardial infarction.

How to take

Adult dose

Adults: Administer 2-3 g of L-carnitine per day orally in 2-3 divided doses. The dose may be adjusted as appropriate according to age and symptoms.

Precautions

This medication should not be used in patients with hypersensitivity to it. Patients with allergic reactions or hypersensitivity to soybean oil should also avoid this medication. Patients allergic to beans or peanuts should avoid this medication as well. Patients with issues in fat metabolism such as hyperlipoproteinemia, diabetic dyslipidemia, or pancreatitis should use this medication with caution. In particular, when using lipid emulsions together, the dosage of this medication should be adjusted. Temporary nausea, vomiting, abdominal pain, diarrhea, and body odor changes may occur after taking this medication. Allergic symptoms like rash, urticaria, and facial swelling may also occur, so caution is advised. Patients with uremia may experience mild side effects such as muscle weakness, thus monitoring is necessary. Patients at risk of fat overload should regularly check their blood lipid levels to adjust the dosage of this medication as needed. Pregnant women or women who may become pregnant should only take this medication if its benefits are deemed greater than the risks. Breastfeeding women should take this medication cautiously as it may be transmitted through breast milk.

Side effects

  • temporary area
  • vomiting
  • abdominal pain
  • diarrhea
  • body odor
  • rash
  • urticaria
  • facial swelling
  • myasthenia

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

Interactions

Drug interactions

Consult with a doctor or pharmacist if this medication is to be used in conjunction with injectable lipid preparations.

Storage

Store this medication in a tightly sealed container to protect it from exposure to air or moisture. It is recommended to maintain a storage temperature between 1°C and 30°C at room temperature. Proper storage will help maintain the effectiveness of the medication for a longer time.

Appearance and packaging

Appearance

White round film-coated tablets

Package unit

90 tablets (10 tablets/PTP × 9)

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

No questions yet.

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.