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

Other names for this medication:
Alpaz, Alpkair, Alprocalm, Alproz, Alrif, Alzep, Anxiflu, Belfa, Benzolam, Calmtec, Cardilax, Depflu, Eurolam, Finezol, Fluprax, Fluwel, Isorest, Mediprex, Nokzok, Plxna, Samitol, Samrox, Setlan, Tenolam, Tryzo, Xycalm

Similar Products:
Cytoxan, Cordarone, Coumadin, Fasigyn, Glucophage

Also known as: Alprazolam


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

You should not use Alzotime if you have narrow-angle glaucoma, if you also take itraconazole or ketoconazole, or if you are allergic to Alzotime 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 Alzotime. 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.


This section provides information on the proper use of a number of products that contain alprazolam. It may not be specific to Xanax. Please read with care.

Take this medicine only as directed by your doctor. Do not take more of it, do not take it more often, and do not take it for a longer time than your doctor ordered. If too much of this medicine is used for a long time, it may become habit-forming (causing mental or physical dependence) or cause an overdose.

This medicine should come with a Medication Guide. Read and follow the instructions carefully. Ask your doctor if you have any questions.

Swallow the extended-release tablet or tablet whole with a full glass of water. Do not break, crush, or chew it.

If you are using the orally disintegrating tablet, make sure your hands are dry before you handle the tablet. Do not remove the tablets from the bottle until you are ready to take it. Place the tablet immediately on the top of your tongue. It should melt quickly and be swallowed with saliva.

If you are using the oral liquid, measure the dose with a marked measuring spoon, oral syringe, or medicine cup.

Do not eat grapefruit or drink grapefruit juice while you are using this medicine.

The dose of this medicine will be different for different patients. Follow your doctor's orders or the directions on the label. The following information includes only the average doses of this medicine. If your dose is different, do not change it unless your doctor tells you to do so.

The amount of medicine that you take depends on the strength of the medicine. Also, the number of doses you take each day, the time allowed between doses, and the length of time you take the medicine depend on the medical problem for which you are using the medicine.

For anxiety: For oral dosage forms (solution, tablets, or orally disintegrating tablets): Adults—At first, 0.25 to 0.5 milligram (mg) 3 times a day. Your doctor may increase your dose as needed. However, the dose is usually not more than 4 mg per day. Older adults—At first, 0.25 mg 2 or 3 times a day. Your doctor may increase your dose as needed. Children—Use and dose must be determined by your doctor. For panic disorder: For oral dosage form (extended-release tablets): Adults—At first, 0.5 to 1 milligram (mg) taken in the morning once a day. Your doctor may increase your dose as needed. However, the dose is usually not more than 10 mg per day. Older adults—At first, 0.5 mg taken in the morning once a day. Your doctor may increase your dose as needed. Children—Use and dose must be determined by your doctor. For oral dosage forms (solution, tablets, or orally disintegrating tablets): Adults—At first, 0.5 milligram (mg) 3 times a day. Your doctor may increase your dose as needed. However, the dose is usually not more than 10 mg per day. Older adults—At first, 0.25 mg 2 or 3 times a day. Your doctor may increase your dose as needed. Children—Use and dose must be determined by your doctor.


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

Side effects

The most common side effects associated with Alzotime 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.


Studies in women breastfeeding have demonstrated harmful infant effects. An alternative to this medication should be prescribed or you should stop breastfeeding while using this medicine.

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Natural killer-like T-cell lymphoma appearing in the duodenum with recurrence in a variety of extranodal organs. However, neutropenia was generally transient and had a benign clinical outcome, after vaccination with either multiple novel candidates or well-known licensed vaccines. When an RNFL defect on fundus photographs was identified in the quadrant, clock-hour, temporal-superior-nasal-inferior-temporal (TSNIT), deviation, and thickness maps, it was considered a true detection. Acute renal failure associated with autologous bone marrow transplantation. Reciprocal creatinine values tested at 6-month intervals showed no statistical differences between treatment groups at any time point. Three minutes after rocuronium administration, Org 25969 or placebo was given in random order. Adherence and systemic reaction rates to allergy immunotherapy among veterans.

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Feasibility, safety, and efficacy of totally endoscopic coronary artery bypass grafting: multicenter European experience. Among straight chain aliphatic alcohol acetates, hydrolysis rates increased with carbon number up to pentyl alcohol and then decreased. Discriminatory effects of protein kinase inhibitors and calcium ionophore on endothelial ICAM-1 induction. The NMBDs are routinely used in critically ill or injured patients of all ages. Factors Affecting Breathing Capacity and Early Tracheal Extubation After Liver Transplantation: Analysis of 506 Cases.

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Enrollment criteria included pancreatectomy, gastrectomy, operative small bowel obstruction or perforation, ostomy, discharge with a drain, in-hospital complication, and clinician discretion. We used quantitative PCR, Western blotting, electron microscopy, immunohistochemistry and measurements of plasma and tumour catecholamines to assess differences in expression of the transporters in noradrenaline-producing vs adrenaline-producing hereditary tumours. Capsaicin pretreatment also reduced, but did not eliminate, the accumulation of CCK binding sites proximal and distal to ligatures on either cervical trunk. Early TATT allowed a significant reduction in the brace wear duration and resulted in the same outcomes as using the Ponseti method. Here we discuss recent advances in the development of GGDPS inhibitors, including insights gained by structure-function relationships, and review the preclinical data that support the continued development of this novel class of drugs. Therefore our data suggest that the higher TO signal of young platelets is derived, to a significant extent, from their larger volume and granule content. Virus-specific capping of tobacco mosaic virus RNA: methylation of GTP prior to formation of covalent complex p126-m7GMP. Technical improvements in the computational target search for antisense oligonucleotides. Specific tumor selectivity of the treatment can be sustained by the intra- and/or peri-tumoral confinement of the agent.

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Understanding brassinosteroid-regulated mechanisms to improve stress tolerance in plants: a critical review. Radial Head Arthroplasty in the Active Duty Military Service Member With Minimum 2-Year Follow-Up. These data indicate that small changes in the amount or density of compact bone tissue exert a more pronounced influence on its stiffness than would similar changes in trabecular bone. The computer-assisted microscope demands rigid specifications for specimen preparation. Low prevalence of HTLV-I/II infection among HIV-1-infected injecting drug users in Russia. We have extended preclinical work to demonstrate that P4 peptide significantly increases phagocytosis and bacterial killing in samples from a target patient population with severe sepsis.

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Here the adsorption energies and dissociation pathways of CO on clean and defective Fe 110 surface are explored by means of density functional theory. Doppler echocardiographic appearance of cusp tears in tissue valve prostheses. Host-extract induced changes in the secretome of the plant pathogenic bacterium Pectobacterium atrosepticum. We reported that IQGAP1, an actin binding scaffold protein, mediates VEGF-induced activation of gp91phox (Nox2)-dependent NAD(P)H oxidase and EC migration. The in situ localization study of proapoptosis (TRADD, caspase 3) and anti-apoptosis gene products (TRAF2) indicated that these were expressed in the basophilic cytoplasm (infected muscle cell origin) of the nurse cells. Immunohistochemical studies for GLP-1R expression have been hampered previously by the use of unspecific polyclonal antibodies. Therapy for binge eating should result in improvement in self-concept and eating self-efficacy, as well as reductions in binge eating.

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Ventriculoperitoneal shunt infection after bladder augmentation. Although prior studies have observed high resource use among patients with CKD, there is limited exploration of emergency department use in this population and the proportion of encounters related to CKD care specifically. Electrogenerated Chemiluminescence Reporting on Closed Bipolar Microelectrodes and the Influence of Electrode Size. Bacterial populations diversify during infection into distinct subpopulations that coexist within the human body. These results seem to indicate that arginine vasopressin may be related to obsessive-compulsive disorder symptom severity, while 5-hydroxyindoleacetic acid might be associated with drug response. Chaperonins belong to a class of molecular chaperones that have been extensively studied. A single injection of thymostimulin into mice in a dose of 45 micrograms/kg b.w. In addition, protein is seen in somites and proximal regions of the limb buds, tissues in which Hox 2.1 RNA expression was not clearly detected previously by in situ hybridization. Dittmar et al proposed that mixing alone can explain our observed decrease in marine dissolved organic sulfur with age.

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Study on substrate metabolism process of saline waste sludge and its biological hydrogen production potential. Measurements were made of the anteroposterior and mediolateral viewing fields at all distances and holding angles on maximum and minimum zoom. Fastigial nucleus injections labelled terminals in a band along the border between the oculomotor nucleus and the supraoculomotor area that included the Edinger-Westphal nucleus. The enhanced fullerene phase separation was found with a decrease of SRR, while the crystallinity and molecular packing of SM remained unchanged. We constructed a conditionally replication-competent adenoviral vector Ad.Lp-CD-IRES-E1A(control) in which the expression of both the prodrug-activating cytosine deaminase gene and the viral replication E1A gene were driven by the L-plastin tumor-specific promoter. Effective prevention of lethal acute graft-versus-host disease by combined immunosuppressive therapy with prodigiosin and cyclosporine A. Remarks on the assessment of anesthesia relative complexity index without taking notice of the code of the surgical procedure.

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The needs and concerns pepcid dosage cat of patients with advanced breast cancer are changing at every phase of the care intervention. Each patient had ocular surgery more than 6 months before developing scleritis. Parotid gland is the most common location of malignant mixed tumors. The authors blended simulation-based learning (SBL) with an interpretative pedagogical frame in a senior nursing leadership course at a primarily undergraduate university. Vitreomacular traction (VMT) caused visual symptoms in two healthy young adults but spontaneously resolved within four weeks without any sequelae. In the present study, we have shown by single afferent unit recording in the organs of Lorenzini that L-serine-O-phosphate (L-SOP) decreases the resting discharge frequency as well as electrically evoked responses. This review highlights recent discoveries in the cellular and molecular basis of liver regeneration.

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In an in-vitro study, the presence of cryptococcal polysaccharide significantly increased (p less than 0.05) production of p24 antigen after infection of H9 cells with HIV-1-infected H9 cells. Sera from 30 patients with JRA were assayed for RF by latex fixation test (LFT), sensitized sheep cell agglutination test (SCAT), nephelometry, and by ELISA. After controlling for levaquin antibiotic group each other, only the seropositivity for anti-wall enolase antibodies was an independent predictor of a lower risk of fatality, supporting that these mediated the protective effect. The significance of these bacteria may be overlooked due to their fastidious growth, and they are often confused with other strains of streptococci or staphylococci. Three patients treated with the intermediate purity concentrate and one treated with the high-purity concentrate developed symptoms of HIV infection. Interactions between homocysteine concentrations and type 2 diabetes mellitus are observed such that associations between homocysteine and cognitive performance are stronger in the presence of diabetes.

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