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Aaram (Alprazolam)

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Aaram 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). Aaram is mostly used to treat anxiety disorders, panic disorders, and nausea due to chemotherapy. Aaram 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, Alparazole, Alprazan, Alprazolam, Alpronit, Alproz, Alzep, Alzoft, Anzocalm, Axizox, Berest, Cozac, Dexolam, Dipra, Endep, Finezol, Fluzolam, Imprax, Mentolift, Oclam, Omelam, Pronext, Propnix, Restam, Rivcam, Samitol, Selamb, Sinzolam, Somnirest, Synozolam, Tenil, Tenlax, Tenrid, Tenschem, Tensyn, Tenzorid, Tranax, Tranisol, Visram, Zallpam, Zedep, Zeecam, Zeprax, Ziety, Zolark, Zolipax, Zorest

Similar Products:
Differin, Avodart, Cordarone, Medrol, Allegra, Klariger, Tevacycline, Jalyn, Wormex, Zolox, Alfacip, Acichek, Trichostatic, Alzopam, Protonix,

Also known as: Alprazolam


Aaram 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.

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

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


Take this medication by mouth as directed by your doctor. Dosage is based on your medical condition, age, and response to treatment. Your dose may be gradually increased until the drug starts working well. Follow your doctor's instructions closely to reduce the risk of side effects.This medication may cause withdrawal reactions, especially if it has been used regularly for a long time or in high doses. In such cases, withdrawal symptoms (such as seizures) may occur if you suddenly stop using this medication. To prevent withdrawal reactions, your doctor may reduce your dose gradually. Report any withdrawal reactions immediately.Along with its benefits, this medication may rarely cause abnormal drug-seeking behavior (addiction). This risk may be increased if you have abused alcohol or drugs in the past. Take this medication exactly as prescribed to lessen the risk of addiction.When this medication is used for a long time, it may not work as well. Talk with your doctor if this medication stops working well.Tell your doctor if your condition persists or worsens.


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

Side effects

The most common side effects associated with Aaram 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.


Do not use Aaram 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 Aaram 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 Aaram 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

FDA pregnancy category D. Aaram XR can cause birth defects in an unborn baby. Do not use Aaram 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 Aaram XR without telling your doctor if you are breast-feeding a baby.

The sedative effects of Aaram 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 Aaram XR. Do not give this medication to anyone under 18 years old.

Aaram XR pregnancy and breastfeeding warnings (more detail)

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Interpersonal problems, personality pathology, and social adjustment after cognitive therapy for depression. Tumour necrosis factor-alpha soluble receptors type I are related to symptoms and left ventricular function in hypertrophic cardiomyopathy. Arum- and Paris-type infection were found in the same plant species. Single molecule nanocontainers made porous using a bacterial toxin. Later, he again required intensive medical therapy including topically applied echothiophate iodide, epinephrine, and acetazolamide to control his glaucoma. The other 13 patients received intravitreal bevacizumab of 1.25 mg in 0.05 ml.

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Quantitative NMR studies of high molecular weight proteins: application to domain orientation and ligand binding in the 723 residue enzyme malate synthase G. Chondrocyte involvement in the process could be studied by identifying the sequence of alterations in matrix macromolecules as the lesion developed. Taken together, our data show for the first time that JNK, but not ERK, p38MAPK or Akt signaling, plays an important role in CTX III-mediated G2/M arrest and apoptosis in K562 cancer cells. MDMA: fact and fallacy, and the need to increase knowledge in both the scientific and popular press. During June 1999-March 2002, a total of 16 tuberculosis (TB) cases were reported from Chickasaw County, Mississippi (2000 population: 19,440), corresponding to annual TB incidences of 20.5-27.6 cases per 100,000 population. Molecular cloning of an alanine aminotransferase from NAD-malic enzyme type C4 plant Panicum miliaceum. Growth hormone excess with onset in adolescence: clinical appearance and long-term treatment outcome. To evaluate risk-adjusted mortality in remote regions of Oregon before and after implementation of a statewide trauma system.

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A human homologue, JRK/JH8, has been cloned, which maps to 8q24, a chromosomal region associated with several forms of IGE. A rabbit ear model has been developed in which arterial pressure, auricular blood flow conductance, and microvascular perfusion can be followed continuously in conscious animals. The results demonstrate that spatial resolution of a transmission imaging system can be improved by use of a high-resolution source collimator at the price of a moderate decrease in detection efficiency, in comparison to the uncollimated case. The A8344G mutation of the tRNA-lysine gene of the mitochondrial DNA was detected in all tissues at high levels (more than 80 p cent). This database provides a unique opportunity to monitor and review practice at national level. The first eight N-terminal amino acid residues were found to be an important structural determinant and were replaceable by alanine residues, thus enhancing the alpha-helical propensity. Its ocular manifestations have only recently been reported with increasing frequency. A hybrid peptide comprising 7 T-cell determinants has the potential for inducing T-cell proliferative responses that is superior to the potential of a mixture of the T-cell determinants and comparable with that of Cry j 1 and Cry j 2.

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A free radial forearm flap was used to create a penis of normal length and diameter. This case highlights the complexity in the management of HP and that even in the absence of confirmed invasive disease, patients may elect to undergo prophylactic colonic resection. Platelet function screening can identify donors with diet-related platelet dysfunction or with poor recollection of aspirin use. Perinatal spinal cord injury is a relatively uncommon, but a frequently misdiagnosed disorder. Nitric oxide (NO) is an essential messenger molecule in brain, where it is produced in neurons mostly by the activity of the neuronal isoform of nitric oxide synthase (nNOS). As with previously identified GOF mutants, RGS4(S30C/S30F/S30K) demonstrate increased steady state protein levels, however these mutants also demonstrate enhanced GAP activity through an additional mechanism distinct from the increased protein content. We found that EPCs with low ALDH activity (Alde-Low) possess a greater myambutol 400 mg tab ability to proliferate and migrate compared to those with high ALDH activity (Alde-High). More research will be needed to follow the developmental trajectory of executive dysfunction in ADHD over the life cycle and tie this to the developmental neuropsychology of EF. Death was consecutive to perforation of the gastric lesion leading to haemorrhagic vomitis and multiorgan failure.

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Asymmetric cycloisomerization of 1,6- and 1,7-enynes by transition-metal catalysts. Electrographic data on the problem of concomitant work of the cerebral hemispheres. Pathogenicity of Fusarium semitectum against crop pests and its biosafety to non-target organisms. Study of the enamel surface of human teeth with interference and phase contrast microscopy and with light and electron stereomicroscopy. The study aimed to compare the outcome of pregnancy in women with valvular heart diseases. Rapid lipitor generic name dosages deposition of glomerular IgA in BALB/c mice by nivalenol and its modifying effect on high IgA strain (HIGA) mice.

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Improved weight attainment of extremely low-gestational-age infants with bronchopulmonary dysplasia. A first orderlike phase transition is confirmed from the wet to dry state bridged by a narrow region with liquid-vapor oscillations in the intersolute region as the strength of the solute-water attractive dispersion interaction decreases. Association between glycaemic control and serum lipids profile in type 2 diabetic patients: HbA1c predicts dyslipidaemia. With this strategy it should be possible to shorten the diagnosis time. Using such a diverse cohort of virtual patients improves the robustness of the in silico analysis and allows critical hypothesis testing to explore key knowledge gaps. Here, we have investigated variations accumulating in Tomato yellow leaf curl China virus (TYLCCNV), a geminivirus in the genus Begomovirus of the family Geminiviridae. A modular approach to Delta(2)-isoxazolines, latent aldol adducts and polyketide building blocks, is reported. Because of its neuroectodermal origin, SCLC has a number of specific antigens that could be capitalized on as immune targets. Without continuous observation by trained anaesthetists, infusion of remifentanil should not be used casually particularly in non-ventilated patients. Ischemic preconditioning of the kidney consisting of three preliminary episodes of vascular clamping (5 min with 5 min reperfusion periods) also increased the percentage of functionally active mitochondria and prevented activation of NO synthesis without appreciably modifying ROS production.

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