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Alltop (Alprazolam)
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Alltop

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:
Alcalm, Aldip, Alpram, Alpraquil, Alproz, Altok, Alzex, Alzokam, Alzorix, Ambusyn, Anilam, Anquil, Anxigo, Anxigon, Anxilam, Anxorel, Avizolem, Axizox, Axnil, Besquil, Cardilax, Depoxit, Emlol, Flunix, Maxorest, Mcalm, Mentolift, Nitril, Onapract, Optizole, Ozolam, Pralam, Prosanti, Pyrex, Resto, Tenschem, Texidep, Zedep, Zoldac, Zolorel, Zopam

Similar Products:
Lanoxin, Plavix, Luvox, Cordarone, Thorazine, Flonase, Hipres, Vascodil, Zyvox, Raciper, Mozartan, Nidazea, Mediphylline, Glycinova, Sildenafilo,

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

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.

Overdose

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.

Storage

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.

Contraindications

Do not use Alltop XR if you have:

narrow-angle glaucoma; if you are also taking itraconazole (Sporanox) or ketoconazole (Nizoral); or if you are allergic to alprazolam or to other benzodiazepines, such as chlordiazepoxide (Librium), clorazepate (Tranxene), diazepam (Valium), lorazepam (Ativan), or oxazepam (Serax).

Before taking Alltop XR, tell your doctor if you are allergic to any drugs, or if you have:

asthma, emphysema, bronchitis, chronic obstructive pulmonary disorder (COPD), or other breathing problems; glaucoma; kidney or liver disease (especially alcoholic liver disease); a history of depression or suicidal thoughts or behavior; or a history of drug or alcohol addiction.

If you have any of these conditions, you may need a dose adjustment or special tests to safely take this medication.

It is dangerous to try and purchase Alltop XR on the Internet or from vendors outside of the United States. Medications distributed from Internet sales may contain dangerous ingredients, or may not be distributed by a licensed pharmacy. Samples of alprazolam purchased on the Internet have been found to contain haloperidol (Haldol), a potent antipsychotic drug with dangerous side effects. For more information, contact the U.S. Food and Drug Administration (FDA) or visit www.fda.gov/buyonlineguide

FDA pregnancy category D. Alltop XR can cause birth defects in an unborn baby. Do not use Alltop XR without your doctor's consent if you are pregnant. Tell your doctor if you become pregnant during treatment. Use an effective form of birth control while you are using this medication. Alprazolam can pass into breast milk and may harm a nursing baby. Do not use Alltop XR without telling your doctor if you are breast-feeding a baby.

The sedative effects of Alltop XR may last longer in older adults. Accidental falls are common in elderly patients who take benzodiazepines. Use caution to avoid falling or accidental injury while you are taking Alltop XR. Do not give this medication to anyone under 18 years old.

Alltop XR pregnancy and breastfeeding warnings (more detail)

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ECM-bound VEGF189 and VEGF206 have molecular masses consistent with the intact polypeptides. The C57Bl, NRMI and H strains were more sensitive, and the RAP, Swiss and Albino-Rosso more resistent to the lethal effect of the intraperitoneal inoculations. In our progesterone experiments the inhibition of liver function increased with dosage and exposition time. The cause-specific hospitalizations of different employment industries have varied, but the differences in all-cause hospitalizations have remained fairly stable, with the ranking among industries remaining almost the same over the past 35 years. Because of the potential risk of interaction with, and underuse of, conventional medications, it is important to document the prevalence of the use of complementary and alternative medicines (CAMs) in asthmatic children.

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Hygienic problems of planning, building and operating water supply systems. Case report and review of the medical literature from September 1966 to June 1997, using a MEDLINE search. Sub-nephrotoxic cisplatin sensitizes rats to acute renal failure and increases urinary excretion of fumarylacetoacetase. Effects of severe experimental intracranial hypertension on the rabbit brain. We consider the rates of noise-induced switching between the stable states of dissipative dynamical systems with delay and also the rates of noise-induced extinction, where such systems model population dynamics. We aimed to assess quality management of type 2 diabetes care in care groups and outpatient clinics. Nine of the 10 subjects received 250 mg 3 times weekly for periods ranging from 5 to 19 weeks, at which time follow-up examinations were performed on 8 of the 9 treated subjects: 1 subject was lost to follow-up. In this work, a finite-element methodology has been applied to simulate two-phase heterostructures containing a polarizable dielectric inclusion. Techniques to reduce seroma and infection in acellular dermis-assisted prosthetic breast reconstruction.

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Application on gold nanoparticles-dotted 4-nitrophenylazo graphene in a label-free impedimetric deoxynivalenol immunosensor. Changes in tissue glutathione antioxidant system in streptozotocin-induced diabetic rats for a period of 15 weeks were examined. An unusual reaction featuring the cascade annulation of internal alkynes to afford spiro heterocycles as the products has been realized for the first time with a hypervalent iodine reagent as the only oxidant. It is concluded that contraction of vascular smooth muscle is accompanied by a changing pool of reducing equivalents. Dose dependance of insulin-stimulated gastrin release in the dog.

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The study explored the efficiency of the Neurobehavioral Cognitive Status Examination (NCSE) in predicting organic pathology in psychiatric patients. Abstracts from the XIII Scientific Meeting of the Argentine Society of Hypertension. Alkaptonuria is a human hereditary metabolic disease characterized by a very high urinary excretion of homogentisic acid, an intermediary product in the metabolism of tyrosine, in association with ochronosis and arthritis. It appeared to be related to context and the interaction of the methods with context and each other rather than linearly to any given method. For each carrier who agreed to participate a medical history was taken, and muscle-strength assessment by hand-held dynamometry and manual muscle testing and cardiological assessment were done. Effects of steroidal and non-steroidal antiandrogens on wild-type and mutant androgen receptors. Dual energy mammography has been proposed as a technique for accurate measurement of breast density. To assess the effects of abruptly intensified physical training on cardiovascular control. Liver transaminases (ALAT, ALP), malondialdehyde, glucose, triglycerides, total cholesterol, HDL-cholesterol, and glycogen were determined.

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The level of aortic bifurcation, iliac vein confluence, course of the ascending lumbar vein, central sacral vessels, and any vascular variation were mapped. Hamsters with intergeniculate leaflet lesions showed a significantly greater suppression of their wheel running in response to light than the sham-lesioned animals. One section of the survey focused on questions regarding the reproductive and sexual health services provided on the health center site. Ultraviolet irradiation increases the incorporation of radioactivity from caffeine to DNA. Motor nerve hyperexcitability in ALS: its pathophysiology and treatment. The epileptologist was able to correctly assess the diagnosis and treatment of 16/20 patients without knowledge of the VEEG results.

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Magnetotactic bacteria that produce magnetic nanocrystals of uniform size and well-defined morphologies have inspired the use of biomineralization protein Mms6 to promote formation of uniform magnetic nanocrystals in vitro. Calcific band keratopathy associated with the use of topical steroid-phosphate preparations. Early intracranial electrical stimulation studies in animals demonstrated cerebellar connectivity to brain structures involved in cognitive and emotive functions. Computed tomography (CT) volumetry can provide anatomic information on the remnant liver volume but not on functional volume. The benefit of using coils concurrently with a limited number of PEDs is not well documented. Genetics of epilepsy: The testimony of twins in the molecular era. Finally, matchmaking is effected at runtime by choosing the appropriate service provider. Like many other major allergens, it contains an immunodominant T cell-activating region (Bet v 1142-156).

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Isolation and characterization of naturally occurring subclasses of human peripheral blood T cells with regulatory functions. A reformed health care system will not reduce the need for antitrust enforcement. A randomized, double-blind, placebo-controlled trial of deprenyl and thiotic acid in HIV-associated cognitive impairment. CD4dullCD8bright T-lymphocytes have been found only in temporal association with some viral infections. Such genetic attenuation may account for a general decrease seen in titres of rabbit hyperimmune antibodies over time. Escherichia coli mutants that synthesize dephosphorylated lipid A molecules. Do nerve terminals and cell bodies of nigrostriatal dopaminergic neurons of the rat contain similar receptors?. Additionally, we also observed an increase in c-fos mRNA expression in both PVN and SON 6 h after water deprivation, which progressively decreased 24, 48, and 72 h after the onset of water deprivation. CT angiography is of low value for preoperative planning for anterior access to the lumbar spine and should be avoided to prevent radiation-induced damage.

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Spontaneous rupture of the urinary bladder is not a rare complication of radiotherapy for cervical cancer: report of six cases. Hyperactivation of MEK-ERK1/2 signaling and resistance to apoptosis induced by the oncogenic B-RAF inhibitor, PLX4720, in mutant N-RAS melanoma cells. An evaluation of the usefulness of some laboratory tests for the monitoring of therapy in cancer. However, the biochemical effects have not yet been validated in humans with various genetic backgrounds and environmental factors. Aspirates from 24 cases of biopsy-confirmed tubular carcinoma were studied. Survey of insect visitation of ornamental flowers in Southover Grange garden, Lewes, UK. Increased incorporation of arachidonic acid into phospholipids in zymosan-stimulated mouse peritoneal macrophages. Damage of the anterior nervus interosseous (Kiloh-Nevin syndrome). Therefore, to determine the maximal dose tolerable and to verify the results from step 1, we administered the higher daily dosage of 450 mg/m2 in step 2 for four successive cycles with 3-week intervals.

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Assignment of floral fate to lateral meristems is primarily due to the cooperative activity of the flower meristem identity genes LEAFY (LFY), APETALA1 (AP1), and CAULIFLOWER. The continuing loss of hard tissue and, in turn, the low retention of the restorative materials in situ valium pill identifier motivates an in-depth exploration of the failure mechanism of the biomaterials involved. Comparison on newer bubble- and membrane oxygenators in the in-vitro recirculation experiment. Alterations in brain membrane fatty acids can lead to cognitive impairment in older persons. Details of where the food was prepared or obtained were also recorded. In the three-layered epidermis and thereafter (66-160 d estimated gestational age), loricrin became positive in the periderm cells, transglutaminases extended to the entire epidermis, and lamellar granule-associated protein was detected in intermediate cells as well as periderm cells.

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Of 1704 cases, 383 (321 employed and 62 unemployed) underwent vocational rehabilitation. This is the first study to find a significant relationship between the PSADT and the rLR through MRI. Myristoylated alanine-rich C kinase substrates (MARCKS) is a prominent protein kinase C (PKC) substrate that is targeted to the plasma membrane by an aminoterminal myristoyl group. Surfaces have been first modified with aldehyde groups to react with the amino end of the synthesized PNAs. High dose fosfestrol in phase I-II trial for the treatment of hormone-resistant prostatic adenocarcinoma. No trend towards the deterioration of glucose tolerance with increasing amplitude of weight cycles.

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Chromosome segregation ensures the equal partitioning of chromosomes at mitosis. This inhibitor has a very high molecular weight, so that we cannot find it in a higher concentration in the middle-ear-secretory. First, she has steadfastly maintained her vision for dentistry as a major health discipline that continues to mature toward acceptance of responsibility for every aspect of the impact that oral disease could have on the health and welfare of its patients. Lactoferrin (Lf) is a member of the transferrin family of iron-binding anti-bacterial celexa 20 mg image proteins, present in most exocrine secretions, such as saliva, and plays an important role in mucosal defense. C-reactive protein (CRP) is used routinely in many hospitals to evaluate patients with an acute abdomen. This paper presents clinical evaluation of the KAIST-Ewha Colonoscopy Simulator II that is extended from the previous version jointly developed by KAIST and Ewha Womans University. The exposure level of CrA in the mouse using a typical preclinical regimen was measured so as to compare it to reported clinical exposure levels. The expression profile and extracellular release of ESAG9 proteins represents a novel and unexpected aspect of the transmission biology of trypanosomes in their mammalian host. Triclosan concentrations in surface water, sediment, and biota tissue are predicted using a fugacity model parameterized to run probabilistically, to supplement the limited available measurements of triclosan in sediment and tissue.

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Potato (Solanum tuberosum) greenhouse tuber production as an assay for asexual reproduction effects from herbicides. It was concluded that TF-LP may be an efficient targeted drug-delivery system for lung cancer therapy. In recent years, work has been carried out on clustering gene expression microarray data. Detailed assessment of cancer cell metabolism can provide biological information for use in both drug discovery and development of personalized cancer therapy. We suggest that this procedure should be considered as a treatment for recurrent GSI and perhaps for primary GSI. A phenomenon of radioadaptive response was revealed in mice in vivo by tests of chromosome aberrations in bone marrow cells and reciprocal translocations in germ cells. The present review identifies important perioperative concerns in patients with sleep apnea and suggests management strategies. The AdoMetDC decarboxylation reaction depends upon a pyruvoyl cofactor generated via an intramolecular proenzyme self-cleavage reaction. Two of the compounds, 8 and 9, showed K(i) values of 9.4 and 6.3microM against PTP1B, 4- and 7-fold lower values compared to those against TC-PTP. The aim of this study was to re-examine this question by systematically exploring this region with extracellular microelectrodes, in bactrim dosing in renal failure anesthetized and artificially ventilated rats.

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