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Anzal (Alprazolam)

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Anzal 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). Anzal is mostly used to treat anxiety disorders, panic disorders, and nausea due to chemotherapy. Anzal 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:
Aaram, Aderta, Alpramax, Alprocalm, Altalin, Alzam, Anlzium, Anxiflu, Anzal, Avizolem, Depten, Destres, Emlol, Eurolam, Indolam, Isorest, Manzolam, Mebasap, Orten, Poize, Serxanti, Somnarest, Sowel, Synozolam, Tagat, Tensfree, Welnorm, Zeftra, Zoldac, Zoltweet, Zopain, Zopral

Similar Products:
Lamisil, Plavix, Ticlid, Calan, Leukeran, Mircette, Tensicard, Nimipose, Diacon, Daocon, Linaris,

Also known as: Alprazolam


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

You should not use Anzal if you have narrow-angle glaucoma, if you also take itraconazole or ketoconazole, or if you are allergic to Anzal 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 Anzal. 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 Anzal exactly as prescribed by your doctor. Follow all directions on your prescription label. Never use Anzal in larger amounts, or for longer than prescribed. Tell your doctor if the medicine seems to stop working as well in treating your symptoms.

Anzal may be habit-forming. Never share Anzal 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 Anzal 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 Anzal suddenly, or you could have unpleasant withdrawal symptoms. Ask your doctor how to safely stop using this medicine.


If you have been prescribed Anzal for medical reasons, the best way to avoid a Anzal overdose is to adhere to prescribed orders—closely monitor your dose and the time at which you take your medication. Track your Anzal 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.


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 Anzal XR dosage information

Side effects

The most common side effects associated with Anzal 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 performed to date have not demonstrated geriatric-specific problems that would limit the usefulness of alprazolam in the elderly. However, elderly patients are more likely to have unwanted effects (eg, severe drowsiness, dizziness, confusion, clumsiness, or unsteadiness) and kidney, liver, or lung problems, which may require caution and an adjustment in the dose for patients receiving this medicine.

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Chromosomal aberrations of multiple myeloma in Chinese patients at diagnosis: a study by combined G-banding and multicolor spectral karyotyping. These findings suggest that ApoA-I could constitute an important innate immunity effector in trout and perhaps other teleost fish. In addition, arterial inflows at 20 mmHg tended to be lower in each limb segment than flow at higher cuff pressures. The patients of the group C, however, the mean blood levels of the dioxins TEQ in 1998 and 1999 did not differ from those of the normal controls determined in 1996 although some patients in this group showed a high toxic contribution rate of PCDFs TEQ for total TEQ. Functional variant of KLOTHO: a breast cancer risk modifier among BRCA1 mutation carriers of Ashkenazi origin. The mechanism leading to viral persistence and hepatocellular carcinoma, however, has not been fully understood. Comminuted fracture of the navicular bone in predisposition to bifurcation. We suggest to perform urine analysis and culture as the initial study for children with acute FUO and well clinical condition. However, when morphine HCI (10-20 MUM) was administered via intraventricular cannulae following pretreatment with propranolol given intraperitoneally in rats performing free operant (sidman) avoidance, the anti-avoidance effects of the opiate were also attenuated.

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Diagnosis of viral gastroenteritis is an important subject in clinical virology which is mainly determined by the availability of reagents in laboratories, such as in the case of astrovirus. Gene amplification and sequencing have led to the discovery of new pathogens as agents of disease and have enabled us to better classify microorganisms from culture. Terminal duct lobular units are scarce in the nipple: implications for prophylactic nipple-sparing mastectomy: terminal duct lobular units in the nipple. Methods like 24-hour dietary recall and food records are commonly used for this task. Some of the conditions associated with calcium phosphate stones are examined, particularly primary hyperparathyroidism, renal tubular acidosis, and medullary sponge kidney. This supports the theory that there is a phase transition in the 3-K phase region near the bulk Tc. The interference screw was radiolucent, requiring magnetic resonance imaging to visualize its location.

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A direct relationship was found between isotope uptake values and the extent of neoplastic growth. Several genetic alterations have been demonstrated to contribute to the development and progression of melanoma. Assessing microvessel density in gastric carcinoma: a comparison of three markers. Bone regeneration was evaluated by microfocus computed tomography, peripheral quantitative computed tomography, and histological examinations. Membrane permeability, low toxicity, and high quantum yield render the fluorophore attractive for biological applications. In the region IV of DBP, a 6-bp insert that was shown in the Sal-1 allele type was found in SK-1, and a 27-bp insert that was shown in the Papua New Guinea allele type was found in SK-2. The heart disease program has the potential to improve the differential diagnoses of physicians in a typical clinical setting. By pinpointing the interacting residues of the ankyrin repeats of RFXANK, the mechanism of this subtype of severe combined immunodeficiency was revealed. Vitamin A absorption and other blood composition studies in mongolism.

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Expression in 32D IGF-IR cells rhinocort generic otc of a dominant negative mutant of Stat3 (DNStat3) inhibits IGF-I-mediated differentiation. A systematic analysis of the structure and (hyper)polarizability of donor-acceptor substituted polyacetylenes using a Coulomb-attenuating density functional. In growth-restricted fetuses with hemodynamic redistribution and a non-reassuring NST, Doppler assessment of the ductus venosus correlates with adverse perinatal outcome. Also, at certain frequencies the particles will turn 90 degrees in space (turn-over phenomenon). These results suggest that measurement of urine MIF concentration may be useful in monitoring renal transplant patients for acute rejection and as a discriminator from cyclosporine nephrotoxicity.

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Lexicographic ordering: intuitive multicriteria optimization for IMRT. Observation of AT1 and AT2 receptor localization within Neuro-2a cells using immunocytochemistry showed distribution similar to other G-protein coupled receptors with diffuse distribution in the cytosol, perinuclear enrichment and accumulation of receptors on the outer cellular periphery with extension into the neurites. We investigated the roles of PKC in the regulation of group IIA secreted phospholipase A(2) ( biaxin tablet sPLA(2)-IIA) expression in cytokine-stimulated rat fibroblastic 3Y1 cells. The data from patients having received grafts from HPA compatible donors were compared to data from patients having received grafts that were mismatched in HPA allotypes in the GVH direction. Inhibition of Candida albicans biofilm formation by antimycotics released from modified polydimethyl siloxane. Low level of physical activity was related to a lower concentration of serum apo B, and higher energy expenditure from household physical activity had a reverse relationship with serum apo B and triglyceride levels. Diabetes, hyperglycemia, and the cardiac surgery patient: introduction. Decidualization did not occur in the senescent animal until 108 hours of development and the appearance of glycogen in the antimesometrial stroma was further delayed until 120 hours of development in the aged female. Introduction of a functional-docking algorithm for protein-protein complexes. Changes of autonomic regulatory processes in the course of therapy in health resorts.

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It is suggested that improving the management of pediatrics surgical conditions would significantly reduce morbidity. The aim was to evaluate the possible impact of the dystrophin loss on the gastrointestinal propulsion in mdx mice (animal model for DMD). The recently characterised p53 homologue, p73, has been mapped to chromosome 1p36, a region often found deleted in neuroblastoma. Nephritis is usually detected by the presence of proteinuria, especially elevated albumin excretion. The OAR were applied to consecutive patients 18 years and over presenting with acute ankle and foot injuries to the ED of an urban teaching hospital. To evaluate Fcgamma receptor (FcgammaR) expression on synovial macrophages from rheumatoid arthritis (RA) patients and to determine whether this expression correlates with the production of the proinflammatory cytokines tumor necrosis factor alpha (TNFalpha), interleukin-1beta (IL-1beta), IL-12, and matrix metalloproteinase 1 (MMP-1). Regulation of Caenorhabditis elegans body size and male tail development by the novel gene lon-8. Superposition of the nonphysiological substrate alpha-D-fructofuranose onto the atomic positions of dideoxyimino-D-glucitol is not possible due to the steric restrictions of the active site. T2 was lengthened in both infarcted and remote myocardium and was influenced by the occurrence of no-reflow.

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Sub-shot-noise microscopy: imaging of faint phase objects with squeezed light. Ultrastructurally, dense core granules were identified in the cytoplasm. Nonsteroidal anti-inflammatory drugs have become increasingly popular, with more than 90 million prescriptions being written annually. We hypothesised that the upregulation of procollagen gene expression in cardiac fibroblasts, in response to cyclic mechanical load, is mediated by one or more members of the MAP kinase family. Activation of protease-activated receptors in astrocytes evokes a novel neuroprotective pathway through release of chemokines of the growth-regulated oncogene/cytokine-induced neutrophil chemoattractant family. Endogenous release of tissue factor pathway inhibitor by topical application of an ointment containing mucopolysaccharide polysulfate to nonhuman primates.

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