Alprazolam
The active substance of Xanax is alprazolam. It belongs to a group of medicines called benzodiazepines (medicines with anxiolytic action). Xanax is indicated for the treatment of symptoms of anxiety disorders in adults, only in situations where the symptoms are severe, prevent normal functioning, or are very troublesome for the patient. This medicine is intended for short-term use only.
Xanax should not be taken by children and adolescents under 18 years of age.
Before starting treatment with Xanax, the patient should discuss it with their doctor:
Episodes of hypomania and mania have been reported in association with the use of Xanax in patients with depression. Before planned surgery, the doctor should be informed about the use of Xanax.
The patient should tell their doctor about all medicines they are currently taking or have recently taken, as well as any medicines they plan to take.
If the patient is pregnant or breastfeeding, thinks they may be pregnant, or plans to have a child, they should consult their doctor before taking this medicine. The use of Xanax is not recommended during pregnancy. If the medicine is used during pregnancy or if the patient becomes pregnant while taking alprazolam, they should be examined for potential fetal risk. If it is necessary to administer the medicine in the last period of pregnancy, high doses should be avoided and the newborn should be monitored. Benzodiazepines pass into human milk in small amounts. Xanax should not be taken during breastfeeding.
Xanax causes impairment of psychophysical fitness. Before taking Xanax, the patient should familiarize themselves with the current local traffic laws. While taking Xanax, the patient should not drive vehicles or operate machines.
If the patient has previously been diagnosed with intolerance to some sugars, they should contact their doctor before taking the medicine.
The medicine contains less than 1 mmol (23 mg) of sodium per tablet, which means the medicine is considered "sodium-free".
Each tablet of this medicine contains 0.11 mg of sodium benzoate.
This medicine should always be taken according to the doctor's instructions. In case of doubts, the patient should consult their doctor or pharmacist. Xanax is available in the following doses: 0.25 mg, 0.5 mg, 1 mg, 2 mg. Treatment should last as short as possible. The doctor should frequently assess the patient's condition and the need to extend treatment, especially if the severity of the symptoms decreases and may not require pharmacological treatment. The total treatment time should not exceed 2-4 weeks. Long-term treatment is not recommended. When starting treatment, the doctor will inform the patient about the limited duration of therapy, the gradual reduction of the dose during withdrawal of the medicine, and the possibility of withdrawal reactions. During the use of benzodiazepines, including Xanax, dependence and emotional or physical dependence may develop. This risk may increase with the dose and duration of treatment, so the smallest effective dose should be used for the shortest possible time, and the need for continued treatment should be frequently assessed with the doctor. Recommended dose The dose is determined by the doctor based on the severity of symptoms and the individual patient's response to treatment. If severe side effects occur after administration of the initial dose, the doctor may decide to reduce the dose. Symptomatic treatment of anxiety disorders The recommended initial dose is 0.25 mg or 0.5 mg three times a day. The doctor may decide to increase it, depending on the patient's needs, to a maximum daily dose of 4 mg divided into smaller doses, taken throughout the day.
Xanax should not be taken by children and adolescents under 18 years of age.
Use in patients with severe liver failure is contraindicated.
The recommended initial dose is 0.25 mg two or three times a day. If necessary, the doctor may decide to gradually increase the dose, depending on the patient's tolerance to the medicine. If side effects occur, the doctor will decide to reduce the initial dose.
Taking a higher than recommended dose of Xanax may cause: ataxia (lack of coordination), drowsiness, speech disorders, coma, and respiratory depression. If worrying symptoms occur, the patient should immediately contact their doctor.
A double dose should not be taken to make up for a missed dose.
The patient should not stop taking Xanax on their own. Since the treatment is symptomatic, after its discontinuation, the symptoms of the disease may return. The doctor will decide to gradually reduce the dose. In case of any further doubts related to the use of this medicine, the patient should consult their doctor.
Like all medicines, Xanax can cause side effects, although not everybody gets them. If any of the following side effects persist or are troublesome, the patient should inform their doctor. The occurrence of some side effects depends entirely on the individual patient's susceptibility and the dose of the medicine. Side effects are usually observed at the beginning of therapy. They disappear as treatment continues or when the dose is reduced.
In addition, especially in patients taking other psychotropic medicines, with mental disorders, or abusing alcohol, a paradoxical reaction may occur with symptoms such as anxiety. Other side effects have been observed rarely or very rarely: motor disorders, epilepsy, psychotic symptoms, a feeling of changed self, agranulocytosis (a significant decrease in the number of granulocytes), allergic reactions, or anaphylaxis (severe allergic reactions). Benzodiazepines may cause physical and psychological dependence. If physical dependence occurs, sudden discontinuation of Xanax may cause withdrawal symptoms: headache, muscle pain, increased anxiety, feeling of tension, agitation, disorientation, irritability, feeling of changed environment or self, impaired hearing, stiffness, and paresthesia of limbs, hypersensitivity to light, noise, and touch, hallucinations, and seizures. These symptoms are usually more severe in patients treated for a long time, with high doses of benzodiazepines, and in the case of sudden or rapid discontinuation of the medicine.
If any side effects occur, including any side effects not listed in this leaflet, the patient should tell their doctor, pharmacist, or nurse. Side effects can be reported directly to the Department of Monitoring of Adverse Reactions to Medicinal Products of the Office for Registration of Medicinal Products, Medical Devices, and Biocidal Products Al. Jerozolimskie 181C 02-222 Warsaw tel.: +48 22 49 21 301 fax: +48 22 49 21 309 website: https://smz.ezdrowie.gov.pl By reporting side effects, more information can be collected on the safety of the use of the medicine.
The medicine should be stored in a place invisible and inaccessible to children. Do not store above 25°C. Do not use this medicine after the expiry date stated on the packaging. The expiry date refers to the last day of the specified month. Medicines should not be disposed of via wastewater or household waste containers. The patient should ask their pharmacist how to dispose of medicines that are no longer used. This will help protect the environment.
Lavender, elliptical-oval tablets, scored, marked with "Upjohn 90" on one side and a score line on the other side of the tablet. The packaging contains 30 tablets in PVC/PVDC-Al blisters in a cardboard box. For more detailed information, the patient should contact the marketing authorization holder or the parallel importer.
Viatris Hellas Ltd
154 51 N. Psichiko, Athens Greece
Pfizer Italia S.r.l. Localita Marino del Tronto 63100 Ascoli Piceno, Italy Pfizer Ireland Pharmaceuticals Little Connell, Newbridge County Kildare, Ireland
Delfarma Sp. z o.o. ul. Św. Teresy od Dzieciątka Jezus 111 91-222 Łódź
Polfarmex S.A. ul. Józefów 9 99-300 Kutno Delfarma Sp. z o.o. ul. Św. Teresy od Dzieciątka Jezus 111 91-222 Łódź Greek marketing authorization number: 23877/26-06-1995 Parallel import authorization number: 137/09 Date of leaflet approval: 15.07.2024
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