Viewing nowAlprazolam 0.4 mg Tablet (Alprazolam)
Alprazolam 0.4mg
Tablet · Prescription medication
Hwa In Pharmaceutical Co., Ltd.

MFDS item code 199203462 · Approved 1992.03.10 · Insurance code 657200480
Relief of symptoms of anxiety disorders, anxiety accompanying depression, panic disorder, and psychosomatic disorders
This medication is used for the treatment of anxiety disorders and for the short-term relief of anxiety symptoms. It also alleviates anxiety accompanying depression and reduces symptoms of anxiety, tension, depression, and sleep disturbances that occur in psychosomatic disorders related to the gastrointestinal and colon. It is effective in managing symptoms of panic disorder. Therefore, this medication helps to improve various anxiety-related conditions.
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. ○ Adults 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 can cause severe drowsiness or respiratory cessation if taken with narcotics, so it should only be used at the minimum effective dose and duration when absolutely necessary. This medication can be habit-forming, so patients taking it should be carefully monitored as per the physician's instructions, and any remaining medication should be stored and disposed of safely to prevent misuse. This medication should not be administered to patients with certain conditions or those taking certain medications, especially those who are at risk, such as patients with acute angle-closure glaucoma, severe myasthenia gravis, severe respiratory failure, and severe liver failure. Caution should be exercised when using this medication in individuals with heart, liver, kidney problems, elderly patients, frail patients, or those with respiratory diseases. Use of this medication may lead to drowsiness, decreased concentration, and reduced motor skills, so it is advisable to avoid driving or operating hazardous machinery. If used for an extended period, regular blood tests and liver function tests should be conducted, and abrupt discontinuation can lead to withdrawal symptoms or seizures, so the dosage should be tapered off gradually. This medication should be used with caution in patients with depression, as it can sometimes cause sudden mood changes or aggressive behavior. This medication may increase the effects of other central nervous system depressants, alcohol, and narcotic analgesics, leading to serious side effects; therefore, concomitant use should be avoided or discussed with a physician. During pregnancy, especially in the last three months, this medication should not be taken; while breastfeeding, caution is necessary as it can be excreted in breast milk affecting the baby. It is advisable to avoid use in children and adolescents under the age of 18, as safety and efficacy have not been established. In the event of overdose, symptoms such as severe drowsiness, coma, and respiratory distress may occur, and immediate medical attention should be sought for appropriate treatment. This medication should be kept out of reach of children and stored in the original container to prevent misuse or degradation.
Not everyone experiences these, and they can vary from person to person.
This medication should be stored in a tightly closed container to prevent air or moisture from entering, away from direct sunlight, and at room temperature. This way, its effectiveness can be maintained for a long duration and deterioration can be prevented.
Orange round tablet
30 tablets/bottle, 200 tablets/bottle
Even with the same ingredient, strength, dosage form and how it is taken can differ.
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Tablet · Prescription medication
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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.