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Alpraquil (Alprazolam)

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Alpraquil 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). Alpraquil is mostly used to treat anxiety disorders, panic disorders, and nausea due to chemotherapy. Alpraquil 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:
Aderta, Alpranex, Alpraquil, Alpron, Alprose, Alzep, Balmusa, Depwell, Fluwel, Fultop, Nitril, Notens, Orten, Pacyl, Prolam, Richpram, Somnia, Somnirest, Sowel, Tenil, Tranisol, Viprax, Wycalm, Ziety, Zolin, Zolran, Zomark, Zopain, Zorest

Similar Products:
Ilosone, Clozaril, Nuvigil, Avana, Mestinon, Imdur, Xenical, Rebetol, Aziphar, Atolife, Meprate, Trigabantin, Kloryl, Ultrax, Triamizide,

Also known as: Alprazolam


Alpraquil (alprazolam) is a benzodiazepine (ben-zoe-dye-AZE-eh-peen). It is thought that alprazolam works by enhancing the activity of certain neurotransmitters in the brain.

Alpraquil is used to treat anxiety disorders and anxiety caused by depression.

Alpraquil is also used to treat panic disorders with or without a fear of places and situations that might cause panic, helplessness, or embarrassment (agoraphobia).

It is dangerous to purchase Alpraquil on the Internet or outside the United States. The sale and distribution of medicines outside the U.S. does not comply with safe-use regulations of the Food and Drug Administration (FDA). These medications may contain dangerous ingredients, or may not be distributed by a licensed pharmacy.


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 Alpraquil dosage information


If you have been prescribed Alpraquil for medical reasons, the best way to avoid a Alpraquil overdose is to adhere to prescribed orders—closely monitor your dose and the time at which you take your medication. Track your Alpraquil 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 at room temperature away from light and moisture. Do not store in the bathroom. Keep all medications away from children and pets.Do not flush medications down the toilet or pour them into a drain unless instructed to do so. Properly discard this product when it is expired or no longer needed. Consult your pharmacist or local waste disposal company for more details.

Side effects

The most common side effects associated with Alpraquil 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.


Before taking Alpraquil, tell your doctor or pharmacist if you are allergic to it; or to other benzodiazepines (such as diazepam, lorazepam); or if you have any other allergies. This product may contain inactive ingredients, which can cause allergic reactions or other problems. Talk to your pharmacist for more details.Before using this medication, tell your doctor or pharmacist your medical history, especially of: severe lung/breathing problems (such as COPD, sleep apnea), liver disease, kidney disease, drug or alcohol abuse, glaucoma.This drug may make you dizzy or drowsy. Do not drive, use machinery, or do any activity that requires alertness until you are sure you can perform such activities safely. Avoid alcoholic beverages.Before having surgery, tell your doctor or dentist about all the products you use (including prescription drugs, nonprescription drugs, and herbal products).Older adults may be more sensitive to the side effects of this drug, especially loss of coordination and drowsiness. These side effects can increase the risk of falling Alpraquil is not recommended for use during pregnancy due to the potential for harm to an unborn baby. Consult your doctor for more details.This drug passes into breast milk and may have undesirable effects on a nursing infant. Therefore, breast-feeding while using this drug is not recommended. Consult your doctor before breast-feeding.

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Phase cancellation effects can compromise the integrity of ultrasonic measurements performed with phase sensitive receiving apertures. Experimental results comparing the proposed algorithm with a few state-of-the-art SAEAs on both benchmark problems up to 30 decision variables as well as an airfoil design problem demonstrate that the proposed algorithm is able to achieve better or competitive solutions with a limited budget of hundreds of exact FEs. Lymphocytotoxic activity was found in undiluted sera or diluted from 1/2 to 1/8. Here we report an alternative culturing method, based on growth on solid media which is independent of the ability of a fungus to grow in liquid culture. Nuclear morphologic and morphometric analyses of nodular poorly differentiated lymphocytic lymphoma: assessment of small cleaved nuclei. Biosynthesis of a major lipofuscin fluorophore in mice and humans with ABCR-mediated retinal and macular degeneration.

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In other members of the family, who present with the same bone disorder, involvement of the cranial nerves was limited to the facial nerve, either uni or bilaterally, with a partially or totally regressive evolution. Lipoprotein(a)-activated immunity, insulin resistance and new-onset diabetes. Systematic review on the proteomic profile of Mycobacterium tuberculosis exposed to drugs. Other radiologic studies (arteriography and inferior venacavography) should be used as complementary studies in selective patients. No significant differences were observed in the 5-year disease-free survival rates or in the 5-year survival rates. Liposome chromatography: liposomes immobilized in gel beads as a stationary phase for aqueous column chromatography. In the day and night trials, there were significant correlations between urinary trichlormethiazide and its effects (urine volume, urinary sodium and chloride) in both groups of rats. The most toxic substances (LC50 (based on survival/EC50 (based on total progeny) less than 10 mg/L) were metallic Cu, tertiary dodecyl mercaptan, an antioxidant TIA-RCO T-424, Cu(NO3)2.3H2O, K2Cr2O7, NALCO 7139--a flocculent, DOWFAX 2EP--a surfactant, TB-66--an algicide and ammonia. A comparison of the effects of left stellate ganglion stimulation (SGS) on central and aortic hemodynamics has been made in chloralose-anesthetized mongrel (M), and greyhound (GH) dogs. Moreover, some compounds possessed comparable activities against carmine spider mite (Tetranychus cinnabarinus) and oriental armyworm (Mythimna sepatara) with spirotetramat.

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The reduced number of GH-R positive tumours found with PCR may be explained by the extraction method of RNA from paraffin sections. Experimental animal studies are necessary if the results of minimally invasive oncological surgery are to be improved. Ultrasound is equal to other imaging methods in detecting complications (fistulas, abscess, stenosis). The present review gives an update on the biochemistry, biology and clinical aspects of hepoxilin-based drug development. The occurrence of diabetes mellitus was investigated in additional T2DM patients of various ages. Insular amyloidosis and diabetes mellitus in a crab-eating macaque (Macaca fascicularis). Analysis of the lacZ sequences from two Streptococcus thermophilus strains: comparison with the Escherichia coli and Lactobacillus bulgaricus beta-galactosidase sequences. Effectiveness of various programs of immunocorrective therapy in chronic infectious-inflammatory diseases.

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Postnatal development of the vascular pattern in the rat telencephalic pia-arachnoid. An incident example is used in the article that illustrates how the new medication called flagyl tool is applied during the investigation and how the results of its application look. Although biguanides are widely used in the treatment of non-insulin- dependent diabetic patients, the underlying mechanism for their antidiabetic effects is not fully understood. A review of four prospective randomized trials including 253 patients with borderline tumors. A decreased ability of irradiated vascular segments to generate PGI2 upon PDGF stimulation described here might cause haemostatic imbalance and subsequent radiation-induced lesions. Artificial neural network analysis of data from multiple in vitro assays for prediction of skin sensitization potency of chemicals. This prospective cohort study, a component of Phases I and II of the Ontario Prehospital Advanced Life Support (OPALS) Study, was conducted in 21 Ontario communities with BLS-D level of care, and included all adult arrests of presumed cardiac etiology according to the Utstein Style Guidelines. A case is presented of a five-year-old with an intra-oral wound which, left untreated for eleven days, failed to resolve.

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