Medication info
Thiosid Tablets (Thioctic Acid)

Thiosid Tablets (Thioctic Acid)

Prescription medicationTabletOral
Ingredient · strength
Thioctic Acid›200mg / 1 tablet
Manufacturer / importer
(Huons Co., Ltd.)
Appearance
Green round film-coated tablets
Packaging
30 tablets/bottle, 500 tablets/bottle
Approval status
Active

MFDS item code 200302121 · Notified 2003.04.04 · Insurance code 670602300

Summary

Main use
Relief of diabetic polyneuritis
Who takes it
Adults
Adult dose
Adults: Unless otherwise prescribed, administer 600mg of thioctic acid orally once daily, 30 minutes before a meal, without chewing, with a small amount of water. Adjust the dose as appropriate according to age and symptoms.

Ingredients

Manufacturer
(Huons Co., Ltd.)

Efficacy & effects

Relief of diabetic polyneuritis

  • Diabetic polyneuropathy
View approved original text

This medication helps alleviate the symptoms caused by diabetic polyneuropathy. It improves nerve damage due to diabetes, reducing pain and sensory abnormalities, and has the effect of protecting the patient's nerve function. It is used to decrease the discomfort in the daily life of patients.

How to take

Adult dose

Adults: Unless otherwise prescribed, administer 600mg of thioctic acid orally once daily, 30 minutes before a meal, without chewing, with a small amount of water. Adjust the dose as appropriate according to age and symptoms.

Precautions

This medication should not be used by patients who have had hypersensitivity reactions. Also, due to a lack of clinical experience in children and adolescents, it should not be administered to them. This medication contains lactose, so it should not be given to patients with genetically determined lactose intolerance. Digestive symptoms such as nausea, vomiting, diarrhea, and gastrointestinal pain may rarely occur when taken. Allergic reactions like skin rash, hives, and itching may also occur infrequently. There is a possibility of hypoglycemic symptoms such as dizziness, sweating, headache, and visual disturbances due to falling blood sugar levels. Taste disturbance has been reported infrequently. Consumption of alcohol may decrease the therapeutic effect of this medication; therefore, diabetic neuropathy patients are advised to avoid alcohol. This medication may interact with certain metal compounds, reducing its effectiveness, so caution is required. When taken in combination with insulin or oral hypoglycemic agents, blood sugar may drop too low; hence, careful monitoring of blood sugar control is needed initially. This medication should not be taken concurrently with iron, magnesium, or calcium preparations, and if taken 30 minutes before breakfast, these preparations should be avoided during meals. Consultation with a physician is recommended for use during pregnancy or breastfeeding, and it is best not to be administered while breastfeeding. In case of overdose, severe toxicity symptoms such as altered consciousness, seizures, hypoglycemia, and multiple organ damage may occur, requiring immediate medical attention. This medication should be kept out of the reach of children and stored in its original container to prevent quality degradation and misuse.

Side effects

  • Nausea
  • vomiting
  • diarrhea
  • gastrointestinal pain
  • skin rash
  • urticaria
  • itching
  • hypoglycemia
  • dizziness
  • sweating
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  • headache
  • visual disturbance
  • taste disturbance
  • indigestion
  • frequent urination
  • palpitations
  • abdominal bloating
  • altered consciousness
  • psychomotor agitation
  • seizures
  • lactic acidosis
  • shock
  • rhabdomyolysis
  • hemolysis
  • disseminated intravascular coagulation
  • bone marrow suppression
  • multiple organ dysfunction

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

Storage

This medication may be sensitive to air or moisture; therefore, it must be stored in a tightly sealed container. It is advisable to maintain the storage temperature between 1 degree and 30 degrees Celsius. This helps to preserve the effectiveness of the medication for a longer period.

Appearance and packaging

Appearance

Green round film-coated tablets

Package unit

30 tablets/bottle, 500 tablets/bottle

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.