Apocuron Tablets (Aplocualone)
Afloqualone 20mg
Prescription medication
Korea Hyutec Pharmaceutical Co., Ltd.
MFDS item code 202100044 · Approved 2021.01.05
This product's status changed to Expired on 2026.01.05. It may no longer be sold, so consult a doctor or pharmacist before taking it.
Improvement of spastic paralysis (e.g., cerebral palsy) and muscle tension (e.g., low back pain)
This medication helps improve muscle tension associated with cervical syndrome and low back pain. Additionally, it is used to alleviate spastic paralysis symptoms caused by various central nervous system disorders such as cerebrovascular diseases, cerebral palsy, and spastic spinal cord palsy. It is also effective for spastic paralysis due to nerve damage such as post-traumatic sequelae or post-surgical sequelae. Thus, this medication is useful for improving muscle stiffness and rigidity symptoms caused by various neurological disorders. Overall, this medication is used to alleviate muscle tension and spastic paralysis symptoms, thereby enhancing patients' motor function.
Adults: Administer afloqualone 20㎎ orally three times daily. Adjust the dose according to age and symptoms.
This medication contains lactose and should not be used by patients with hereditary lactose intolerance. When taking this medication, mental dizziness or drowsiness may occur, and occasionally, symptoms such as headaches may appear. Gastrointestinal effects may also occur, leading to nausea, decreased appetite, abdominal pain, and discomfort in the stomach, and rare cases of vomiting or diarrhea may occur. There may be symptoms of increased sensitivity to light, so if such symptoms occur, the medication should be discontinued and a consultation with a doctor should be made. Additionally, if allergic reactions such as rashes or itching occur, immediate discontinuation of the medication and appropriate measures should be taken. This medication may cause fatigue or lethargy, and in rare instances, symptoms such as edema, tinnitus, frequent urination, and oral inflammation may occur. During the course of treatment, drowsiness or dulled reflexes may occur, so driving or operating hazardous machinery should be avoided. Women who are pregnant or may become pregnant should only use this medication when the benefits of treatment outweigh the risks, as its safety is not assured. Breastfeeding is also not established for safety, so it should be avoided if possible, and if absolutely necessary, breastfeeding should be discontinued. There is insufficient safety experience with this medication in children, therefore safety has not been fully confirmed. In elderly patients, caution is required as physical functions may be diminished, including reducing the medication dosage.
Not everyone experiences these, and they can vary from person to person.
This medication is sensitive to light, so it should be stored in a special container that does not allow light. Furthermore, it is important to keep the medication at room temperature between 1 degree and 30 degrees Celsius to maintain its effectiveness.
White round film-coated tablets
30 tablets/bottle, 1000 tablets/bottle
Even with the same ingredient, strength, dosage form and how it is taken can differ.
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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.