Viewing nowAzolac Tablet 0.25 Milligram (Alprazolam)
Alprazolam 0.25mg
Tablet · Prescription medication
Unimed Pharmaceutical Co., Ltd.

MFDS item code 199203480 · Approved 1992.10.21 · Insurance code 649501400
Relief of symptoms of anxiety disorders, anxiety associated with depression, panic disorder, and psychosomatic disorders
This medication is used to treat anxiety disorders and to temporarily alleviate anxiety symptoms. It also helps improve anxiety symptoms associated with depression. It is effective for symptoms of anxiety, tension, depression, and sleep disturbances caused by psychosomatic disorders. It is also used for the treatment of panic disorder and is utilized in improving overall mental instability.
Determine the dose individually to achieve maximum benefit. The usual daily doses listed below are suitable for most patients, although higher doses may be required. In such cases, increase the dose slowly to avoid adverse effects. The risk of dependence may increase with the dose and duration of treatment. Therefore, use the lowest effective dose for the shortest possible duration and frequently reassess the need to continue treatment. 1. As alprazolam, the initial dose is 0.25-0.5㎎ per dose, 3 times daily, with a maximum dose of 4㎎ daily. For older adults, patients with hepatic impairment, and debilitated patients, the initial dose is 0.25㎎ per dose, 2-3 times daily. Reduce the dose if adverse effects occur at the initial dose. 2. Psychosomatic disorders Administer this medicine orally at 1.2㎎ daily in 3 divided doses. If increasing the dose, increase it gradually to a maximum of 2.4㎎ daily and administer orally in 3-4 divided doses. For older adults, the initial dose is 0.4㎎ per dose, 1-2 times daily, with a maximum dose of 1.2㎎ daily. 3. Panic disorder Start with 0.5㎎ of this medicine and, depending on the patient's response, increase the dose by no more than 1㎎ at intervals of 3-4 days, to an average daily dose of 5-6㎎ divided into 3-4 doses. When discontinuing treatment, reduce the dose by no more than 0.5㎎, usually at intervals of 3 days; an even lower dose reduction may be required.
This medication is a benzodiazepine drug that acts as a sedative and is used for the treatment of anxiety or panic disorders. Care should be taken when coadministering this medication with narcotics, as it may result in severe sedation, respiratory depression, coma, and in severe cases, death. This medication can lead to abuse and dependence, hence patients should be monitored by a physician and adhere to appropriate dosages and durations during treatment. Taking this medication with alcohol or other central nervous system depressants increases the risk; therefore, it should not be taken together with such substances. This medication should not be administered to certain patients, for example, those with acute angle-closure glaucoma, severe myasthenia gravis, severe respiratory failure, or severe liver dysfunction. Patients with hypersensitivity to this medication or those with certain genetic disorders, pregnant women in late pregnancy, and patients with alcohol or drug dependence should also not receive this drug. Patients with compromised heart, liver, or kidney function, the elderly, and those with brain injury should use this medication cautiously, as symptoms of ataxia or excessive sedation may appear. Drowsiness or decreased attention may occur during treatment, so driving or operating hazardous machinery should be avoided. In the case of long-term use, it is advised to undergo regular blood tests and liver function tests. Abrupt discontinuation of this medication may lead to withdrawal symptoms or seizures; thus, the dosage should be gradually reduced according to the physician's instructions. This medication may cause hypomania or manic symptoms when administered to patients with depression, so caution is required. During pregnancy, it may affect the fetus, so it is particularly safe not to administer it in late pregnancy. Breastfeeding women should also avoid administering this medication as it may be transmitted through breast milk and affect the newborn, hence they should either refrain from use or discontinue breastfeeding. This medication can interact with various drugs; therefore, if any other medications are being taken, a doctor or pharmacist should be informed. In the case of overdose, symptoms such as drowsiness, impaired coordination, coma, and respiratory depression may occur, requiring immediate emergency treatment. This medication is not recommended for children, as safety and efficacy have not been established.
Not everyone experiences these, and they can vary from person to person.
This medication should be stored in a sealed container to protect it from air and moisture. Additionally, it should be stored at room temperature, not too hot or too cold.
White oval tablet
30 tablets/bottle, 200 tablets/bottle
Even with the same ingredient, strength, dosage form and how it is taken can differ.
Viewing nowAlprazolam 0.25mg
Tablet · Prescription medication
Unimed Pharmaceutical Co., Ltd.

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Alprazolam 0.25mg
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Alprazolam 1mg
Tablet · Prescription medication
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Kwangdong Pharmaceutical Co., Ltd.

Alprazolam 0.25mg
Tablet · Prescription medication
Kwangdong Pharmaceutical Co., Ltd.
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.