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Ezoprax (Alprazolam)

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Alprazolam, available under the trade name Xanax, is a potent, short-acting benzodiazepine anxiolytic—a minor tranquilizer. It is commonly used for the treatment of anxiety disorders, especially of panic disorder, but also in the treatment of generalized anxiety disorder (GAD) or social anxiety disorder. It was the 12th most prescribed medicine in the United States in 2010. Ezoprax, like other benzodiazepines, binds to specific sites on the GABAA receptor. It possesses anxiolytic, sedative, hypnotic, skeletal muscle relaxant, anticonvulsant, amnestic, and antidepressant properties. Ezoprax is available for oral administration as compressed tablets (CT) and extended-release capsules (XR).

Other names for this medication:
Aderta, Albiz, Alcicalm, Alltop, Almac, Alpram, Alprastan, Alprazan, Alprine, Alprocalm, Alprocontin, Alprogard, Altok, Alwe, Alzac, Alzoax, Alzoft, Alzokam, Alzot, Anlzium, Anxitab, Azoslip, Besquil, Dexolam, Eurolam, Fludep, Fluzolam, Fultop, Jolistar, Kurelam, Morecalm, Notence, Plaxid, Resolin, Somaspas, Tancalm, Tenan, Tenschem, Tranisol, Trapose, Trustin, Xycalm, Zeftra, Zolax, Zolipax, Zopam

Similar Products:
Symmetrel, Provera, Avana, Sovaldi, Glyburide, Duricef, Mellaril

Also known as: Alprazolam


Alprazolam is used to relieve symptoms of anxiety, including anxiety caused by depression. It is also used to treat panic disorder in some patients.

Alprazolam is a benzodiazepine. Benzodiazepines belong to the group of medicines called central nervous system (CNS) depressants, which are medicines that slow down the nervous system.

This medicine is available only with your doctor's prescription.


Take this medication by mouth as directed by your doctor. Dosage is based on your medical condition, age, and response to treatment. Your dose may be gradually increased until the drug starts working well. Follow your doctor's instructions closely to reduce the risk of side effects.This medication may cause withdrawal reactions, especially if it has been used regularly for a long time or in high doses. In such cases, withdrawal symptoms (such as seizures) may occur if you suddenly stop using this medication. To prevent withdrawal reactions, your doctor may reduce your dose gradually. Report any withdrawal reactions immediately.Along with its benefits, this medication may rarely cause abnormal drug-seeking behavior (addiction). This risk may be increased if you have abused alcohol or drugs in the past. Take this medication exactly as prescribed to lessen the risk of addiction.When this medication is used for a long time, it may not work as well. Talk with your doctor if this medication stops working well.Tell your doctor if your condition persists or worsens.


Seek emergency medical attention or call the Poison Help line at 1-800-222-1222. An overdose of alprazolam can be fatal.

Overdose symptoms may include extreme drowsiness, confusion, muscle weakness, loss of balance or coordination, feeling light-headed, and fainting.


Store the medicine in a closed container at room temperature, away from heat, moisture, and direct light. Keep from freezing.

Keep out of the reach of children.

Do not keep outdated medicine or medicine no longer needed.

Ask your healthcare professional how you should dispose of any medicine you do not use.

It is very important to protect the orally disintegrating tablets from moisture. Remove and throw away any cotton packaging from the medicine bottle when you first use the medicine.

Detailed Ezoprax XR dosage information

Side effects

The most common side effects associated with Ezoprax are:

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Side effect occurrence does not only depend on medication you are taking, but also on your overall health and other factors.


You should not take Ezoprax if:

you also take itraconazole or ketoconazole (antifungal medicines); or you have a history of allergic reaction to any benzodiazepine (alprazolam, diazepam, lorazepam, Ativan, Klonopin, Restoril, Tranxene, Valium, Versed, and others).

To make sure Ezoprax is safe for you, tell your doctor if you have ever had:

breathing problems such as COPD (chronic obstructive pulmonary disease) or sleep apnea (breathing that stops during sleep); drug or alcohol addiction; depression, mood problems, or suicidal thoughts or behavior; or kidney or liver disease (especially alcoholic liver disease).

Tell your doctor if you are pregnant or plan to become pregnant. Alprazolam may harm an unborn baby. Avoid taking this medicine during the first trimester of pregnancy.

If you use Ezoprax while you are pregnant, your baby could become dependent on the drug. This can cause life-threatening withdrawal symptoms in the baby after it is born. Babies born dependent on habit-forming medicine may need medical treatment for several weeks.

You should not breastfeed while using alprazolam.

Ezoprax is not approved for use by anyone younger than 18 years old.

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The impact of antiretroviral therapy (ART) on herpes simplex virus type-2 (HSV-2) replication is unclear. The Choices programme: a simple, front-of-pack stamp making healthy choices easy. In the presence of preoperative dysphagia and oesophageal dysmotility, this procedure has engendered concern in certain regards. The American Public Health Association and the population problem. Considerations in deep brain stimulation (DBS) for pediatric secondary dystonia. Implementation of a Clinical Pathway for Chest Pain in a Pediatric Emergency Department. The ability of VIP-VPAC1 axis signals to evoke development of a novel type of Th17 cells demonstrates the unique specificity of neuroregulatory mechanisms in the immunological environment.

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After NGAL-silenced HK-2 cells were subjected to hypoxia/reoxygenation, the levels of LC-3 II and beclin-1 were lower than those in the controls with blank vector, whereas the levels of LC-3 II and beclin-1 in were higher than those in the ones in which 400 ng/mL recombinant NGAL was imuran ulcerative colitis reviews added. This paper presents the fabrication of a sensitive, fully depleted (FD), electrolyte-insulator-semiconductor field-effect transistor (EISFET) made with a silicon-on-insulator (SOI) wafer of a thin 10-30 nm active SOI layer. Results of treatment of acute and chronic urinary tract infections with Bactrim or its single components sulfamethoxazole and trimethoprim. Importantly, hydrolysis of AMP was sufficient to reactivate deadenylation by miRNAs or Smaug, suggesting that AMP accumulation, rather than ATP depletion, caused the inhibition of the deadenylation reaction. Recombination in interpopulation hybrids of the copepod Tigriopus californicus: release of beneficial variation despite hybrid breakdown. Myelopoietic response in tumour-bearing mice by an aggregated polymer isolated from Aspergillus oryzae. A 57-year old woman underwent lung transplantation for non-specific interstitial pneumonia.

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We report a case of 27-year-old male who had non-dystrophic myotonia with periodic paralysis and two heterozygous mutations, E950K in CLCN1 and F1290L in SCN4A. Lack of a common framework has hindered application of the extant literature in practice, and, until now, there were no evidence-based guidelines for ensuring data quality in MRA. We designed a new bioinformatics framework to handle each aspect of the miRNome: whole expression profiles, isomiRs distribution, non-templated additions distributions, RNA-editing or mutation. To describe the age-specific prevalence of common eye diseases causing bilateral visual impairment and estimate the total number of Australians with cause-specific visual impairment. On serum and hepatic beta-glucuronidase activities in hepatic diseases in children. 3D-TVS or 3D-SIS was not more efficient can you take prilosec with thyroid medication than 2D-TVS or MRI for assessment of myometrial invasion in endometrial cancer. The CO formed has been shown to function as a neurotransmitter, and may be involved in nociceptive signaling.

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In the last decade, basic cancer research has produced remarkable advances in our understanding of cancer biology and cancer genetics. Diversity Oriented Synthesis of Indoloazepinobenzimidazole and Benzimidazotriazolobenzodiazepine from N(1)-Alkyne-1,2-diamines. Our results indicate that the XbaI (-) allele of the GLUT1 gene might be a genetic marker of NIDDM with DN, and this genetic susceptibility is independent of its retinopathy in Chinese subjects. Association of Body Mass Index and Body Mass Index Change with Mortality in Incident Peritoneal Dialysis Patients. Univariate and multivariate analyses of prognostic factors for pneumonia evolution were carried out. Repetitive transcranial magnetic stimulation is as effective as electroconvulsive therapy in the treatment of nondelusional major depressive disorder: an open study. HER3 over-expression and overall survival in gastrointestinal cancers. Retrospective Biological Dosimetry at Low and High Doses of Radiation and Radioiodine Impact on Individual Susceptibility to Ionizing Radiation. Children who were born in 1986 and immunized with hepatitis B vaccine at birth were followed up at least once a year. Trifluoroethanol-induced conformational transition of the C-terminal sterile alpha motif (SAM) of human p73.

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Chronic mild stress in submissive mice: Marked polydipsia and social avoidance without hedonic deficit in the sucrose preference test. Guiding transcranial brain stimulation by EEG/MEG to interact with ongoing brain activity and associated functions: A position paper. Closing the Brief Case: Anaerobiospirillum succiniciproducens Bacteremia and Pyomyositis. In confocal microscopy, the proliferative change in the subepithelial layer was observed as bright, highly refractive tissue interspersed with small spaces void of cells, and was especially evident at the wound edges of the peripheral side. We determined direct costs of materials, direct costs of personnel and labor, indirect costs, and depreciation. Myotonic dystrophy type 1 (DM1) is a multisystemic disorder caused by a CTG repeat expansion in the DMPK gene. To better understand the evolution of this family, we investigated the correlation between sequence and structural repeats within this family and the evolution and molecular adaptation of Pot II genes through computational analysis, using the putative ancestral domain sequence as the basic repeat unit. In contrast, no single nucleotide polymorphism (SNP) mutations were observed, either in vivo or in vitro. To follow transformation, various parameters: cell type, proliferation, clonogenicity, karyotypes and tumorigenicity, were studied at different passages. When finer instruments were used for retraction and the duration of medial opening was shortened to less than 10 min, the SNAP of the IAN was always preserved at this stage.

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