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Alpraday (Alprazolam)

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Alpraday 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). Alpraday is mostly used to treat anxiety disorders, panic disorders, and nausea due to chemotherapy. Alpraday 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:
Alfresh, Alpkair, Altalin, Altok, Alzac, Alzam, Alzom, Anxiflu, Anxigo, Anxizam, Axnil, Azoslip, Benzax, Depten, Dipra, Elzopam, Exprex, Fledore, Manzolam, Maxorest, Mebrin, Morecalm, Niravam, Orten, Pizolam, Selam, Silam, Zeftra, Zodia, Zolark, Zomark

Similar Products:
Yasmin, Luvox, Singulair, Rhinocort, Levlen, Microzide, Paxil, Bactrim, Zudena, Bpzide, Preterax, Anzitor, Antiplatt, Lozaril, Ondeo,

Also known as: Alprazolam


Alpraday XR (alprazolam) is in a group of drugs called benzodiazepines (ben-zoe-dye-AZE-eh-peens). Alprazolam affects chemicals in the brain that may become unbalanced and cause anxiety.

Alpraday XR is used to treat anxiety disorders, panic disorders, and anxiety caused by depression.

Alpraday XR may also be used for other purposes not listed in this medication guide.


This section provides information on the proper use of a number of products that contain alprazolam. It may not be specific to Alpraday XR. 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 Alpraday for medical reasons, the best way to avoid a Alpraday overdose is to adhere to prescribed orders—closely monitor your dose and the time at which you take your medication. Track your Alpraday 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 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 Alpraday 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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Single Photon Emission Computed Tomography-Computed Tomography (SPECT/CT) gains an important part of diagnostics in patients with osteochondral lesions (OCL). The subsequent hypotensive/hypertensive response was due to the chemicals acting on targets in different parts of various body systems. Cnn dynamics drive centrosome size asymmetry to ensure daughter centriole retention in Drosophila neuroblasts. Alternative renin-angiotensin system pathways in adipose tissue and their role in the pathogenesis of obesity. The studies on spontaneous motor activity in mice and conditioned avoidance responding (CAR) in rats showed a dose-dependent depression of the central nervous system in treated animals. Analysis of variation in the human beta-globin gene cluster using a novel DHPLC technique. Fusion progeny were characterized by random spore analysis because the markers present in the strains were not amenable to the conventional four-on-four selection procedure. Surprisingly, the function of the central nervous system and muscle, as assessed in a locomotion assay, are only marginally affected. Every step in the recording procedure--calibration, collection, processing and presentation of the data--can be automatically controlled by the computer.

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The prostate-specific antigen (PSA) doubling time (PSADT) has been shown to be a surrogate for survival in earlier stages of prostate cancer, but its utility as a predictor in HRPC is unknown. Reflex pupil-dilatation by way of the cervical sympathetic nerve. Hamilton depression scores of the patients correlated positively with activation of the left and right ventral amygdala during expectation of negative stimuli. Genogeography of human populations: computer mapping of population genetics data. Nkx2.2 targeted to the pancreas by UTMD induces pancreatic progenitor cell proliferation and differentiation with subsequent islet regeneration and cure of STZ-induced diabetes for three months. Retroviral CYP2B1 transfer followed by CPA treatment highly sensitized pancreatic tumor cells NP-9, NP-18, and NP-31, and led to stabilization of tumor growth in a pancreatic tumor model. The concentrations of C1 inactivator and C3b inactivator were measured in the peripheral lymph of leg of normal men and udenafil review compared with the concentrations in serum. We used different types of backgrounds: either with isoluminant red and green areas or with black and white areas.

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A sensitive and reliable semi-quantitative real-time PCR assay to detect JAK2 V617F in blood. Recently, a maturation model that incorporates a sigmoidal E(max) type model has been proposed for the estimation of morphine clearance in paediatric patients. This report discusses possible explanations for the disparity between the number of people who are chronically infected and the number of people who receive treatment. Fever represents a normal and adaptative response developed in case of host aggression, notably by infectious agents, and is part of a large defense system, the acute phase response. Moreover, MSCs recruit primary FL cells that, in turn, trigger their differentiation into FRCs, making them able to support malignant B-cell survival. In addition, adrm1 knockout cells also exhibit abnormal initiation of development. Tumor necrosis factor (TNF)-like weak inducer of apoptosis (TWEAK) is a recently identified proinflammatory cytokine of the TNF superfamily. Processes of care and medical complications in patients with stroke. The incidence of head louse infestation increased from 5.2 per 1000 in 1977 to 18.1 per 1000 in 1979, and then declined to 3.6 per 1000 in 1987. We found that myr-PKI and another myristoylated peptide potently and specifically potentiated I(f) via a mechanism that did not involve PKA inhibition and that was independent of the peptide sequence, Protein Kinase C, or phosphatidylinositol-4,5-bisphosphate.

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Responses of the pituitary-adrenal system of mice to an environment of high temperature and humidity. Although low-energy shock wave (SW) is adopted to treat ischemic diseases because of its pro-angiogenic properties, the underlying mechanism remains unclear. Furthermore, Myf5- or Myod-expressing anlagen are identified in craniofacial myogenesis. After discontinuation of mycophenolate mofetil, 5 of the 9 patients relapsed. Overall, short-term Nordic walking training induces positive changes in knee muscle strength and functional performance in women with low bone mass. Similarly, C-reactive protein values remained within the normal range during the study period in all groups. This retrospective study comprised 28 children (31 eyes) who had cataract surgery with primary IOL implantation. Effect of straight chain fatty acids on seizures induced by picrotoxin and pentylenetetrazole in mice. Following a case report, the major clinical findings, pathophysiologic findings, diagnoses, and use of various therapeutic modalities are discussed.

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Hyperhomocysteinemia has been linked with atherosclerosis, including that in the cerebral vasculature. Bardet-Biedl syndrome gene variants are associated with both childhood and adult common obesity in French Caucasians. As a corollary, expression of the genes coding for three fibrogenic cytokines, transforming growth factor-beta, tumour necrosis factor and interleukin-4, was elevated. The parameters in the system are estimated from experimental data, and the model is simulated for a normal human subject following a loss of blood. Toxicity was signalled as inhibition of dextranase activity, assayed fluorimetrically. We previously showed that the calcium-binding protein S100A4 is overexpressed during the progression of prostate cancer (CaP) in humans and in the TRAMP (transgenic adenocarcinoma of the mouse prostate ultram breastfeeding ) mouse model. These discoveries may validate the potential effectiveness of therapeutic work with a wide variety of difficult personality disorders and addictive forms of pathology.

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