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Zolorest (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. Zolorest, like other benzodiazepines, binds to specific sites on the GABAA receptor. It possesses anxiolytic, sedative, hypnotic, skeletal muscle relaxant, anticonvulsant, amnestic, and antidepressant properties. Zolorest is available for oral administration as compressed tablets (CT) and extended-release capsules (XR).

Other names for this medication:
Albiz, Alprowon, Alzolite, Alzorix, Anilam, Anquil, Aryalam, Censir, Copax, Depflu, Depwell, Dexolam, Ecsit, Esteem, Finezol, Fledore, Flunix, Isorest, Morecalm, Pecalm, Pronil, Proprazolam, Prosanti, Pyrex, Selamb, Setlan, Silam, Tenrid, Tensyn, Zepro, Zolipax, Zoltweet

Similar Products:
Antabuse, Epivir, Zudena, Nuvigil, Depakote, Acticin, Combivent, Levlen

Also known as: Alprazolam


Zolorest is a benzodiazepine (ben-zoe-dye-AZE-eh-peen). Alprazolam affects chemicals in the brain that may be unbalanced in people with anxiety. Zolorest is used to treat anxiety disorders, panic disorders, and anxiety caused by depression.

You should not use Zolorest if you have narrow-angle glaucoma, if you also take itraconazole or ketoconazole, or if you are allergic to Zolorest or similar medicines (Valium, Ativan, Tranxene, and others).

Alprazolam may be habit-forming. Misuse of habit-forming medicine can cause addiction, overdose, or death.

Do not drink alcohol while taking Zolorest. This medication can increase the effects of alcohol. Alprazolam may be habit-forming and should be used only by the person for whom it was prescribed. Keep the medication in a secure place where others cannot get to it.


Take exactly as prescribed by your doctor. Do not take in larger or smaller amounts or for longer than recommended. Follow the directions on your prescription label. Your doctor may occasionally change your dose to make sure you get the best results.

Do not crush, chew, or break an extended-release tablet. Swallow the pill whole. It is specially made to release medicine slowly in the body. Breaking the pill would cause too much of the drug to be released at one time.

Measure the liquid form of Zolorest with a special dose-measuring spoon or cup, not a regular table spoon. If you do not have a dose-measuring device, ask your pharmacist for one.

Do not swallow the orally disintegrating tablets whole. Allow it to dissolve in your mouth without chewing.

Contact your doctor if this medicine seems to stop working as well in treating your panic or anxiety symptoms.

You may have seizures or withdrawal symptoms when you stop using Zolorest. Ask your doctor how to avoid withdrawal symptoms when you stop using Zolorest.

Keep track of the amount of medicine used from each new bottle. Zolorest is a drug of abuse and you should be aware if anyone is using your medicine improperly or without a prescription.


Seek emergency medical attention if you think you have used too much of this medicine. An overdose of Zolorest XR can be fatal.

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


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 Zolorest XR dosage information

Side effects

The most common side effects associated with Zolorest 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.


Appropriate studies have not been performed on the relationship of age to the effects of alprazolam in the pediatric population. Safety and efficacy have not been established.

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ADAR1 interacts with NF90 through double-stranded RNA and regulates NF90-mediated gene expression independently of RNA editing. Direct arterial blood pressure measurements, monitored continuously over 24 hours, showed that nifedipine significantly reduced systolic and diastolic blood pressures throughout the day and at night. A standard extract named Kohki tea (Maruzen Pharmaceuticals, Onomichi City, Japan) is sold over the counter in Japan as a sweet tea shown to confer many beneficial effects on general health and well-being. Children with intractable epilepsy benefit from early surgical treatment when possible to reduce long-term morbidity. They include pathogens of humans and livestock, agriculturally valuable strains, and several highly abundant marine groups. Various drought-related traits, including root traits, leaf traits, osmotic adjustment capabilities, water potential, ABA content, and stability of the cell membrane, have been used as indicators to evaluate the drought resistance of plants. Recently, effector mechanisms have been shown to play a part in anti-CD154 mAb-induced transplant acceptance in murine models, while this issue remains unresolved for humoral-mediated models.

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We described previously the potent blockade of hepatocyte growth factor-stimulated cell motility, matrix invasion, and epithelial tubulogenesis by synthetic Grb2-Src homology 2 (SH2) domain binding antagonists. Effect of yohimbine on blood pressure in patients with depression and orthostatic hypotension induced by clomipramine. Three-dimensional computational models are developed to investigate flow-mixing and oxygen-transfer characteristics for stationary and pulsating balloons, using the spectral element method. Monoamine-releasing agents, tyramine and 6OHDA, enhanced spontaneous nerve discharges but depressed taste responses. Various biomacromolecules including proteins and polysaccharides are printed on a substrate capped with a bovine serum albumin (BSA) precursor layer to create clear co-patterns of these molecules. Thus, we suggest to include TCS into routine monitoring programmes and to consider it as an important candidate for prioritisation at the European scale. To identify the contributory factors associated with different sites of occlusion and the presence or absence of optic nerve head swelling (ONHS).

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