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Alltop (Alprazolam)

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Alltop 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). Alltop is mostly used to treat anxiety disorders, panic disorders, and nausea due to chemotherapy. Alltop 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:
Actirax, Albiz, Alcalm, Aleez, Almac, Alpanol, Alprazan, Alzac, Alzam, Alzolam, Alzopam, Anxiflu, Anxitab, Aryalam, Azoslip, Cqlam, Dazolam, Deproz, Flumusa, Fluti, Fultop, Jolistar, Nexlpra, Oclam, Omelam, Ozolam, Prozam, Richpram, Sinaday, Sinozol, Sinzolam, Visram, Zolar, Zotin

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Glucophage, Danocrine, Dilantin, Imuran, Maxolon, Alprostadil, Depakote, Abilify, Hytrin, Klonopin, Glimid, Salonimar, Virazole, Endometryl, Ostriol, Lipium, Abbotic, Cinbenon,

Also known as: Alprazolam


Alltop 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.

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

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

Side effects

The most common side effects associated with Alltop 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.


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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Inhibiting effect of phenytoin on nitric oxide production in tissues of gamma-irradiated mice. Previous studies indicate that anesthesia and surgery induce an inflammatory reaction in alveolar macro phages. The progression of a tumor cell from one of benign delimited proliferation to invasive and metastatic growth is the major cause of poor clinical outcome of cancer patients. Idelalisib is a potent selective oral inhibitor of phosphatidylinositol 3-kinase delta and has shown significant clinical activity in B-cell malignancies. Antitumor activities of alkaloids isolated from this plant have been reviewed, while there are only a few studies that examine properties of the whole extract. They code for secreted signaling proteins that are cleaved into an active aminopeptide and a carboxypeptide. Similarly to the results of a previous survey in Okinawa, Noto, and Hokkaido, the main type of lens opacification was cortical in Amami. Understanding how to identify patients who may be most sensitive to treatment is clearly needed to improve the development of these molecules. The 2-5A-dependent nuclease activity of the truncated RNase L could result from the association of these digestion products, as suggested in pull down experiments. Taken together, our findings demonstrate that insulin molecules are susceptible to active estrogenization, and that such modification may alter the action of insulin.

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Reversal of P-gp mediated multidrug resistance in-vitro and in-vivo by FG020318. The recombinantly produced protein is soluble and has a hexa-histidine tag engineered at the N-terminus for ease of purification using metal affinity chromatography. Functional scores such as Constant score and American Shoulder and Elbow Surgeons Standardized Shoulder Assessment Form score were assessed. Excited by illumination at 355 nm, a 4.6-fold increase in the fluorescence signals of PAHs was recorded when MEF substrates were used. On average, students with health insurance are healthier and as a result are more likely to be academically successful. Confocal microscopy revealed that ezrin was associated with free apical membranes of E2-treated cells. Implantable devices to treat atrial fibrillation: real prospects or just new gimmicks?. Univariate and multivariate analyses, as well as receiver operating characteristic curve analysis, were used to evaluate the predictive ability of demographic, clinical, and metabolic PET parameters. Modern notions on the morphology and function of the epithelial barrier of the buccal mucosa are discussed.

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Reproducibility of home blood pressure measurements over a 1-year period. Significance of chaperonin 10-mediated inhibition of ATP hydrolysis by chaperonin 60. These discrepancies are attributed to electrohydrodynamic flow caused by local variations in the electric field at the vicinity of the electrodes, which occur during the reversal voltage. To determine whether estimates of regional cerebral blood flow (rCBF) using xenon computed tomography (XeCT) in children with moyamoya disease can predict stroke risk before and after treatment. Histopathology determined the lesion to be a nerve sheath tumor (neurilemmoma versus neurofibroma). The functional anatomy of inspection time: an event-related fMRI study. Association between Reactive Attachment Disorder/Disinhibited Social Engagement Disorder and Emerging Personality Disorder: A Feasibility Study. We show that yeast centromeres are heavily resistant to removal of UV-induced DNA lesions by two different repair systems, photolyase and nucleotide excision repair.

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When SEC is interfaced to CRIMS, further information (elemental detection) is obtained, enhancing the analytical capability of SEC. In utero first trimester exposure to low-dose methotrexate with increased fetal nuchal translucency and associated malformations. coli strain expressing chlM converted Mg-protoporphyrin IX to Mg-protoporphyrin monomethyl ester, demonstrating that chlM encodes the Mg-protoporphyrin methyltransferase of Synechocystis. This study aimed to observe the therapeutic effect of pentapeptide PLNPK on systemic lupus erythematosus (SLE) in mice, and to study the inhibitory effect of PLNPK on activation of T cells in vivo. The computer databases of the American Board of Pediatrics and the American Board of Internal Medicine were used to identify 1482 individuals who had completed training in combined med/peds residency programs between 1986 and 1995 and who had applied to either board for certification. Common variants of GPC1 gene were genetically involved in BA risk. For some pulmonary conditions surfactant replacement therapy is on the horizon, but for the majority much more needs to be learnt about the pathophysiological role the observed surfactant abnormalities may have. We describe here the first reported case of dermatophytosis occurring in healing herpes zoster lesions. We then apply these evolutionary clues to define putative functions of MAT. Based on a developmental perspective, the data currently available are examined, highlighting the insights gained from this body of work and outlining the conceptual and methodological challenges that still need to be addressed.

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The antibiotic peak salivary levels depended on the type of saliva examined (parotid vs submandibular vs minor salivary gland) and the biochemical method of measurement (high-performance liquid chromatography vs bioassay). Cyclosporin A improves the selection of cells transfected with the puromycin acetyltransferase gene. Development of methods for the determination of vitamins A, E and beta-carotene in processed foods based on supercritical fluid extraction: a collaborative study. Clinical classification, genetic mutation, clinical course, preoperative hearing threshold, high-resolution computed tomography of the temporal bone, and postoperative hearing outcome were assessed. These catastrophic survival rates are to be correlated to systematic relapses that might arise from remaining glioblastoma stem cells (GSCs) left behind after surgery. Super-resolution reconstruction based on incoherent optical aperture synthesis. We found 46 reports of RCTs and CCTs on 14 nonsurgical treatments and 11 literature reviews.

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These results suggest that patients who receive preoperative chemoradiotherapy are potentially immunosuppressed, the preoperative serum transferrin level is a possible predictive marker of postoperative pneumonia, and suppression of factor XIII activity is related to anastomotic insufficiency. The homogeneous discrimination of free components and particle-based assemblies can be extended into the micromolar concentration range. Other systems adaptable to the study of embryogenesis and development in space and to resolve the current reservations are described and their place in future space research is indicated. Internal mammary node lymphoscintigraphy and biopsy in breast cancer. T lymphocyte response to Neisseria gonorrhoeae porin in individuals with mucosal gonococcal infections. To evaluate the agreement between repeat transvaginal sonographic assessments of tubal patency using a combination of air and saline. In this study, we investigated the Vascular endothelial growth factor (VEGF) pathway in the developing lung in an EA-TEF rat model.

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The proto-oncogene c-myc encodes a basic helix-loop-helix leucine zipper transcription factor (c-Myc). Clinical evaluation of the DNA bentonite flocculation test for systemic lupus erythematosus. Photoacoustic imaging is a hybrid imaging modality capable of producing contrast similar to optical imaging techniques but with increased penetration depth and resolution in turbid media by encoding the information as acoustic waves. Extracorporeal Shock Wave Lithotripsy (ESWL) is based on disintegration of the kidney stone by delivering high-energy shock waves that are created outside the body and transmitted through the skin and body tissues. Image reconstruction method in MITAT is always a critical issue. Furthermore, the growth and autotoxin-degrading efficiency of them were analyzed by liquid culturing method and GC-MS to illustrate their autotoxin-degradation characteristics. Cobra venom antigen gave positive absorbance at about 500 pg/ml.

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Children with cancer and central lines, treated at the National Hospital in Norway, were consecutively enrolled in the study. Development of Neutralization Assay Using an eGFP Chikungunya Virus. Three tests (Purdue pegboard test, dynamometer hand-grip strength, upper-extremity test) and a subjective interview were used to evaluate motor performance. Evaluation of 4D dose to a moving target with Monte Carlo dose calculation in stereotactic body radiotherapy for lung cancer. Autophagy induction extends lifespan and reduces lipid content in response to frataxin silencing in C. Of the 13 trials identified, there were five different methods used to report neuropsychiatric adverse events: Grade 1-4 all, Grade 1-4 drug related, Grade 2-4 all, Grade 2-4 drug related, Grade 3-4 all, Grade 3-4 drug related, and adverse events leading to discontinuation. Palliative nursing care for the patient experiencing end-stage renal failure. Assuming there will be a rising level of public awareness, the influence of their use will increase well into the future.

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