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Aaram (Alprazolam)
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Aaram

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

Description

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.

Dosage

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.

Overdose

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.

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 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.

Contraindications

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 www.fda.gov/buyonlineguide

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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This finding indicates that the interaction between ClfA and free fibrinogen is not required for ClfA-mediated functions contributing to S. The importance of AP-1 as a mediator of proliferation and radiation responses is demonstrated by the findings that the expression of JunD, Fra-1 and Fra-2 siRNAs in prostate cancer cells suppress these cellular responses. Apart from being responsive to physiological stimuli such as angiotensin II, glomerular mesangial cells are predominantly activated by agents related to inflammation. The spectral phase interferometry for direct electric field reconstruction is used to characterize the pulse temporally. Loss-of-function CYP2C9 variants improve therapeutic response to sulfonylureas in type 2 diabetes: a Go-DARTS study. Staining for laminin was more confined to the endothelial side of the sheath. In this issue of the British Journal of Pharmacology, Gao et al. government-sponsored cooperative study, in which this laboratory participated, and to samples in a parallel in-house study. Growth of well-aligned gamma-MnO2 monocrystalline nanowires through a coordination-polymer-precursor route. The characterization and the flocculation mechanism of microbial flocculant TJ-F1 with high flocculating activity, produced by Proteus mirabilis from a mixed activated sludge, was investigated.

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