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Zoloid (Alprazolam)
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Zoloid

Zoloid is used to treat anxiety and panic disorders. It belongs to a class of medications called benzodiazepines which act on the brain and nerves (central nervous system) to produce a calming effect. It works by enhancing the effects of a certain natural chemical in the body (GABA). Zoloid is mostly used to treat anxiety disorders, panic disorders, and nausea due to chemotherapy. Zoloid may also be indicated for the treatment of generalized anxiety disorder, as well as for the treatment of anxiety conditions with co-morbid depression. The FDA label advises that the physician should periodically reassess the usefulness of the drug.

Other names for this medication:
Alprop, Alprose, Alzac, Anxorel, Balzam, Besquil, Depflu, Depoxit, Emcalm, Endep, Erazol, Faxtin, Hiprazole, Notence, Oclam, Plaxid, Poize, Procalm, Pronil, Prosanti, Sertakem, Tenan, Zeecam, Zeftra, Zoloid

Similar Products:
Biaxin, Viramune, Lopid, Zebeta, Arava, Atarax, Zudena, Mestinon, Antabuse, Amaryl, Bacbutol, Caverta, Repaglinide, Olzap, Rosatan, Rizatriptan, Disorb, Glimid, Latochek, Postpon,

Also known as: Alprazolam

Description

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.

Dosage

Take Zoloid exactly as prescribed by your doctor. Follow all directions on your prescription label. Never use Zoloid in larger amounts, or for longer than prescribed. Tell your doctor if the medicine seems to stop working as well in treating your symptoms.

Zoloid may be habit-forming. Never share Zoloid with another person, especially someone with a history of drug abuse or addiction. Keep the medication in a place where others cannot get to it.

Misuse of habit-forming medicine can cause addiction, overdose, or death. Selling or giving away this medicine is against the law.

Do not crush, chew, or break a Zoloid extended-release tablet. Swallow the tablet whole. Call your doctor if this medicine seems to stop working as well in treating your panic or anxiety symptoms. Do not stop using Zoloid suddenly, or you could have unpleasant withdrawal symptoms. Ask your doctor how to safely stop using this medicine.

Overdose

If you have been prescribed Zoloid for medical reasons, the best way to avoid a Zoloid overdose is to adhere to prescribed orders—closely monitor your dose and the time at which you take your medication. Track your Zoloid consumption in a notebook or on your phone. If you notice that you are taking a higher dose of the drug, taking the drug more often, or you want to consume more of the drug, talk with your doctor immediately.

Storage

Store at room temperature away from light and moisture. Do not store in the bathroom. Keep all medications away from children and pets.Do not flush medications down the toilet or pour them into a drain unless instructed to do so. Properly discard this product when it is expired or no longer needed. Consult your pharmacist or local waste disposal company for more details.

Side effects

The most common side effects associated with Zoloid 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.

Contraindications

Tell your doctor if you have ever had any unusual or allergic reaction to this medicine or any other medicines. Also tell your health care professional if you have any other types of allergies, such as to foods, dyes, preservatives, or animals. For non-prescription products, read the label or package ingredients carefully.

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The aim of this study was to evaluate the dynamics of autogenous bone graft incorporation process to surgically created defects in rat calvaria, using epifluorescence microscopy. RanGTP, but not RanGDP, was able to displace p62 bound to the importin alpha/beta complex, suggesting that the binding sites for p62 and RanGTP on importin-beta overlap. A new CQSAR program was used in deriving regression equations and calculating the octanol/water partition coefficient and the molar refractivity values. Its sensitivity is higher than that of cystoscopic examination and may become an important ancillary method in the screening of urothelial carcinoma recurrence. The author gives a comparative analysis of the mechanism of biological action of microwaves and laser radiation in the range of molecular to body level. The latter, however, usually refers to a slower progressing, is not or only incompletely able to involution and scarcely reacts to cortisonoids.

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Thermal dependence of chemosensory activity in the carotid body superfused in vitro. Altered collagen of human pathological fibroblasts impairs the synthesis of fibronectin. Present role of the sanatorium for pulmonary tuberculosis patients. Although clone A-4 is non-tumorigenic, clones I-7 and II-4 exhibit benign and malignant tumorigenic phenotypes, respectively, after subcutaneous injection into athymic nude mice. A process evaluation of social model residential substance abuse programs was conducted by the Alcohol Research Group (ARG) from September 1995 to April 1996. A light pulse during the late subjective night induced a phase advance shift only in the morning component, while a light pulse during the early subjective night induced a phase delay shift only in the evening component.

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The study aims to investigate associations between behavioural and psychological symptoms is taking xanax while breastfeeding of dementia (BPSD) and abnormal premorbid personality traits. The multivalency strategy is valuable for moving multivalent AMPs toward clinical applications. We have applied a recently developed method called CAST-ELISA to evaluate the degree of leukocyte stimulation by specific allergen. The present experiment was designed to investigate acute responses of the microcirculation of skeletal muscle to local interarterial infusion of sodium nitroprusside (a direct donor of nitric oxide and thus an endothelium-independent vasodilator) or acetylcholine chloride (which stimulates endothelium release of endogenous nitric oxide) during reperfusion after 4 hours of warm ischemia. From lancets to lasers: the evolution of the US health care system (Part I). In Calpodes larvae the feet are orientated axially in the direction of the segmentally repeating gradient and may extend for several cell diameters. Immunologically-specific resistance to infection with particular reference to staphylococcal mastitis.

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The white matter showed consistent immunoreactivity for AMPA receptor subunit GluR2/3 and KA receptor subunits GluR6/7 and KA2. Possible implications of host plant choice on the digestive physiology of A. In addition, comparison of the pre- and posttreatment isolates from 1 patient documented outer membrane protein changes temporally linked with the development of resistance. Immunofluorescence confocal microscopy reveals that TIF1alpha exhibits a finely granular distribution in euchromatin of interphase nuclei, while it is mostly excluded from condensed chromatin and metaphase chromosomes. In addition, the concepts have practical value as they can be used in designing new systems as well as understanding or evaluating currently operating systems.

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