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Alpradol (Alprazolam)

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Alpradol 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). Alpradol is mostly used to treat anxiety disorders, panic disorders, and nausea due to chemotherapy. Alpradol 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, Aldep, Alprop, Alprotame, Alwe, Alzac, Alzoax, Alzolam, Alzomax, Anilam, Anxitab, Anzilum, Avizolem, Azicalm, Calmef, Deproz, Endolam, Exiten, Exprex, Fledore, Fluprax, Fluti, Imprax, Indolam, Manzolam, Prolam, Restam, Silam, Tensfree, Xerodep, Zamitol, Zeprax, Zocam, Zoloid, Zolyde, Zopax

Similar Products:
Minipress, Compazine, Panadol, Persantine, Plavix, Theolair, Inderal, Flomax, Revozip, Azpan, Almac, Citerid, Concore, Novatrex, Benrik, Tryline,

Also known as: Alprazolam


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.


This section provides information on the proper use of a number of products that contain alprazolam. It may not be specific to Alpradol. 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.


Seek emergency medical attention if you think you have used too much of this medicine. An overdose of Alpradol XR can be fatal.

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


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 Alpradol XR dosage information

Side effects

The most common side effects associated with Alpradol 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 Alpradol 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 Alpradol 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 Alpradol 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.

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

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Haploinsufficiency of ANG has thus been implicated in ALS pathogenesis, and ANG has been shown to promote motor neuron survival both in vitro and in vivo. The power of molecular approaches for the analysis of schistosomes at the population and individual level is now apparent, especially for S. The angiographic quality of the successful angioplasty revascularization at each site was assessed, and the subsequent restenosis rate was determined. These findings thus suggest a role for cell-specific mRNAs containing opa repeats during mouse spermatogenesis. The human T-cell leukemia virus type I (HTLV-I)-encoded transcriptional activator protein Tax is strongly implicated in HTLV-I pathogenesis. Knee scores reflect the difficult reconstructive challenges that are inherent in patients who require a V-Y quadricepsplasty. Transient optical studies of interfacial energetic disorder at nanostructured dye-sensitised inorganic/organic semiconductor heterojunctions. This increased persistence was accompanied by a reduction in inflammatory nodules around adult filariae. Promising findings suggest that cognitive remediation may be useful in addressing cognitive deficits in early-course and prodromal participants.

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In explants grown in either control media or with the sense oligonucleotide two rods of cartilage separated by a cartilage free area located in the medial region of the mandible were formed. Synthesis, spectral characterization, DNA interaction, radical scavenging and cytotoxicity studies of ruthenium(II) hydrazone complexes. Eight point mutations arise within the mutant lineage, only one of which appears on chromosome 2. External validity lent support to the distinctions between DSM-III-R ODD and CD, and between MODD, ICD, and ACD. It is shown that a treatment to evaluate mixed stains within the scope of a hypotheses testing approach yields a formula identical to one proposed recently by Weir und coauthors. Manganese superoxide dismutase removes superoxide radicals in mitochondria, and thus protects mitochondria from oxidative injury. Presence of a micro-organism of the Rickettsial group in cerebrospinal fluid sediment and in blood cultures of patients with encephalitis or encephalomyelitis. Benefits administrators--and their employers--can no longer ignore the skyrocketing costs of health care. By testing on large sets of images (in both 2D and 3D), we explore the effects of using different image representations and different statistical shape constraints. We propose that cyclic expression of clock genes is suspended during cellular differentiation.

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Its broader spectrum of activity and availability in oral and intravenous forms allow a flexible approach in the management of fungal infections. Endoscopic gross anatomy findings of the thoracic air sac of the turkey. Both glutathiolation and inhibition of AR are reversible upon subsequent incubation of the cells with fresh media without NO donors. Clathrin-mediated endocytosis of high density lipoprotein3 in human intestinal Caco-2 cells. All DRGs were initially analyzed to determine the potential for erroneous payment. We have studied the role of macrophages in the production of IgG anti-DNA autoantibodies by (NZB x NZW)F1 mice (B/W).

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Anatomical study of the configuration and architecture of the intraspinal ligaments of the lumbar segment of the human spine. The association between baseline lung function and bronchial responsiveness to methacholine. To study the subcellular localization of E2 in live cells, the enhanced green fluorescent protein (EGFP) was fused to the N terminus of E2. Urine calcium excretion studies as a means of selection of hormone dependent tumors. Further, it is important to investigate the three distribution channels resulting from the research because of their importance in terms of information asymmetry. Twenty-one patients who had undergone total thyroidectomy for thyroid cancer were recruited.

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No acetylcholinesterase reaction product was found in cat erythroblasts. The decrease in outer medullary PO2 was prevented by injection of furosemide but not by injection of mannitol. Chylous pleural effusion associated with primary lymphedema and lymphangioma-like malformations. For another six patients, the stroke occurred during physical exertion. Epitope- rocaltrol calcitriol capsules blocking enzyme-linked immunosorbent assays for the detection of serum antibodies to west nile virus in multiple avian species. In 1969 Canada began programs at both the national and provincial levels to lower prescription drug prices. A promising class of peptidomimetic farnesyltransferase inhibitors was discovered through the replacement of the terminal AAX motif of the CAAX-tetrapeptide by 2-acylamino-5-aminobenzophenones. Gender and cross-cultural differences in the association between somatic symptoms and emotional distress were investigated, using data from the World Health Organization Collaborative Project on Psychological Problems in General Health Care. New York City voluntary hospitals would need 85 percent of their total assets to repay their debt, while the comparison groups would use less than 60 percent.

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The maximum growth rates were 0.063 h-1 in pure culture and 0.014 h-1 in coculture (corresponding growth yields: 8.9 and 6.0 g dry weight/mol glycerol). Stimulatory molecular 4-1BB could promote division and survival of T cells and enhance effector activity including cytokine production. PAR3 can mediate thrombin-triggered phosphoinositide hydrolysis and is expressed in a variety of tissues, including human bone marrow and mouse megakaryocytes, making it a candidate for the sought-after second platelet thrombin receptor. Comparison of the amino acid sequence of FlaB2 to sequences present in data banks showed significant similarity with the core flagellins of other spirochaetes, in particular with a FlaB2 protein from Treponema phagedenis. Self-reported health problems, health is xanax an ssri drug care utilisation and unmet health care needs of elderly men and women in an urban municipality and a rural area of Bhaktapur District of Nepal. Gaelic games (Gaelic football and hurling) are indigenous Irish sports with increasing global participation in recent years. The renal AQP2 expression levels in KKAy mice aged between 5 and 24 weeks were determined using Western blotting. In contrast to the African and New Guinean patients where upper body involvement was common, burns in these four patients were of moderate severity and involved primarily the lower body. The drug was administered subcutaneously starting 24 h before SIV inoculation, and treatment continued for an additional 28 days. Typically, it presents as a large benign multicystic liver mass in children younger than three years, amenable to complete resection.

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