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Xanax (Alprazolam)

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Xanax is a potent, short-acting benzodiazepine anxiolytic—a minor tranquilizer. It is commonly used for the treatment of anxiety disorders, especially of panic disorder. It's also used in the treatment of generalized anxiety disorder (GAD) or social anxiety disorder. It was the 12th most prescribed medicine in the United States in 2010. Xanax, like other benzodiazepines, binds to specific sites on the GABAA receptor. It possesses anxiolytic, sedative, hypnotic, skeletal muscle relaxant, anticonvulsant, amnestic, and antidepressant properties. Xanax is available for oral administration as compressed tablets (CT) and extended-release capsules (XR).

Other names for this medication:
Acalm, Albiz, Alfix, Alpron, Alrif, Alzolite, Alzoset, Anxigo, Apsolam, Azoslip, Balzam, Cardilax, Faxtin, Hiprazole, Jolistar, Luzarn, Morecalm, Omelam, Prozolam, Sowel, Synozolam, Texidep, Trustin, Tryzo, Zepro, Zoldac, Zopain

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Floxin, Colospa, Detrol, Fosamax, Moduretic, Flonase, Sinequan, Prevacid, Adalat, Provera, Ifitrim, Albol, Aviband, Permiskin, Lapros, Milfadin, Amodipin,

Also known as: Alprazolam


Xanax 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.

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

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


Usual Adult Dose for Anxiety:

Immediate-release tablets: 0.25 to 0.5 mg orally administered 3 times a day -Maximum dose: 4 mg/day

Usual Adult Dose for Panic Disorder:

Immediate-release tablets: 0.5 mg orally administered 3 times a day -Maximum dose: 10 mg/day Extended-release tablets: -Initial dose: 0.5 to 1 mg orally once a day -Maintenance dose: 3 to 6 mg orally per day, preferably in the morning -Maximum dose: 10 mg/day Comments: -The lowest possible effective dose should be administered and the need for continued treatment reassessed frequently. -Dosage should be reduced gradually when discontinuing therapy or when decreasing the daily dosage. -The daily dosage may be decreased by no more than 0.5 mg every 3 days; however, some patients may require an even slower dosage reduction. -The dose of extended-release tablets may be increased at intervals of 3 to 4 days in increments of no more than 1 mg per day. -The times of administration should be distributed as evenly as possible throughout the waking hours.

Usual Geriatric Dose for Anxiety:

Elderly or debilitated patients: Immediate-release tablets: 0.25 mg orally administered 2 or 3 times a day.

Usual Geriatric Dose for Panic Disorder:

Elderly or debilitated patients: Immediate-release tablets: -Initial dose: 0.25 mg orally administered 2 or 3 times a day Extended-release tablets: -Initial dose: 0.5 mg orally once a day Comments: -If side effects develop, the dose may be lowered. -The lowest possible effective dose should be administered and the need for continued treatment reassessed frequently. -Dosage should be reduced gradually when discontinuing therapy or when decreasing the daily dosage.

Detailed Xanax dosage information


Seek emergency medical attention or call the Poison Help line at 1-800-222-1222. An overdose of alprazolam can be fatal.

Overdose symptoms may include extreme drowsiness, confusion, muscle weakness, loss of balance or coordination, feeling light-headed, and fainting.


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 Xanax XR dosage information

Side effects

The most common side effects associated with Xanax 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.


You should not take Xanax if:

you also take itraconazole or ketoconazole (antifungal medicines); or you have a history of allergic reaction to any benzodiazepine (alprazolam, diazepam, lorazepam, Ativan, Klonopin, Restoril, Tranxene, Valium, Versed, and others).

To make sure Xanax is safe for you, tell your doctor if you have ever had:

breathing problems such as COPD (chronic obstructive pulmonary disease) or sleep apnea (breathing that stops during sleep); drug or alcohol addiction; depression, mood problems, or suicidal thoughts or behavior; or kidney or liver disease (especially alcoholic liver disease).

Tell your doctor if you are pregnant or plan to become pregnant. Alprazolam may harm an unborn baby. Avoid taking this medicine during the first trimester of pregnancy.

If you use Xanax while you are pregnant, your baby could become dependent on the drug. This can cause life-threatening withdrawal symptoms in the baby after it is born. Babies born dependent on habit-forming medicine may need medical treatment for several weeks.

You should not breastfeed while using alprazolam.

Xanax is not approved for use by anyone younger than 18 years old.

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The possible mechanism(s) of H-2 effects on chemically induced tumorigenesis are discussed. High-density lipoproteins (HDLs) counteract several adverse biological effects triggered by oxLDLs. Leachate/final pH determined the metal leaching behavior, which changed the speciation of heavy metals in the extraction system. The introduction of even a small gap between the two halves of the plate results in spectral broadening of the transmitted radiation due to a reduction of the cut-off effect. We investigated the following: 1) biocompatibility of the catheter, 2) patency of the system, 3) flow through the system, 4) histology of the inner surface of the catheter, 5) biochemical analysis of blood components adhering to the inner surface of the catheter, and 6) histology of perfused brain. The goal of this study was to develop a method for identification and downstream processing of potentially valuable bioproducts produced by archaea. Thus activation of muscarinic cholinoreceptors within the CNS were a necessary condition for this form of neuronal plasticity.

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Results demonstrated that prefrontal interhemispheric connectivity between the left and right dorsolateral prefrontal cortex correlates with Agreeableness in healthy subjects. Physical interaction between bovine viral diarrhea virus nonstructural protein 4A and adenosine deaminase acting on RNA (ADAR). Some CC neurons contained both CB and PV, suggesting cooperation between these CaBPs in the CC. Animals were instrumented and loaded in compression for 1.5 h at 1 MPa and 1 Hz. Patients were investigated clinically and by colour flow duplex scanning before operation. Adhesion to the French guidelines appears to be moderate for the management of missed early miscarriage and low for the management of incomplete early miscarriage.

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Effects of the neuropeptide Y on estradiol and progesterone secretion by human granulosa cells in culture. The Prospective Association Between Internalizing Symptoms and Adolescent Alcohol Involvement and the Moderating Role of Age and Externalizing Symptoms. Successful treatment of a patient with acute myeloid leukemia with 1 alpha(OH)D3. The target respondents were menopausal or PMW aged 45 to 60 years, with no previous diagnosis of osteoporosis or breast cancer, who attended private clinics across Hong Kong for annual physical examination. We comment on the efficacy, safety and ethics of AIDS vaccine, and the urgent need for a new strategy for AIDS vaccine development. These results suggest that in dual infection, the level of HIV-2 replication depends on the immune status of the patients, with HIV-1 out-replicating HIV-2 as disease progress. This increased HCV RNA expression was associated with the elevated expression of HCV NS3 protein in the hepatocytes. The morphological analysis of the ground and unground enamel was treated with three different self-etching adhesive systems. If that was not possible, a structural piece of bone graft either from the local resection or a local rib was slotted in the posterior column defect to re-establish continual structural posterior bone across the lateral margins of the resection.

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Design of a difference-frequency infrared laser spectrometer for absorption line-shape studies. EMOTLAB: software for studying emotional signaling in economic bargaining games. Using single-strand conformational polymorphism analysis, we have screened a set of sporadic colon cancers for somatic mutations in PTEN and LKB1. Drug nanosuspension is one of the established methods to improve the bioavailability of poorly soluble drugs. The snail Biomphalaria glabrata kills the blood fluke Schistosoma mansoni by a mechanism involving production of hydrogen peroxide, the enzymatic product of cytosolic Cu/Zn superoxide dismutase (SOD1). HRP-encapsulated liposomes were prepared by an extrusion method, and a CL reagent and H(2)O(2) were added into the liposomes suspensions. Significant progress was achieved in recent years in cardiac output determination by bioimpedance. Simulations and experimental results prove the validity of the new method. We therefore propose an extended Samilson-Prieto classification with type A (spherical) and type B (aspherical) and grade I-IV osteophytes.

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Anesthesia for a patient with mitochondrial respiratory chain complex III deficiency. Measurements of active and passive force of horizontal muscles in strabismus. In patients with CS-EAS who attended a comprehensive cancer center, tumors originating in the chest cavity were the leading tumors associated with this syndrome. Ion channels involved in the release of calcitonin gene-related peptide by low pH, prostacyclin and capsaicin in the isolated guinea-pig heart. Transgenic expression of SpmS was found in all of the tissues examined, but the relative SpmS activities varied widely according to the founder animal and the tissue studied. White laboratory rats, weighted 100-160 g, with acute pneumonia, inhale (from 4-th to 8-th days of developing the disease) liposomes.

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