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Alprose (Alprazolam)

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Alprose is commonly used to treat anxiety and panic disorders. It falls into a category of medications called benzodiazepines. They are known to affect the central nervous system components and produce a calming effect, thus decreasing brain activity.

Other names for this medication:
Acalm, Alpam, Altrex, Alzolite, Alzomax, Alzorix, Ambusyn, Betapax, Dazolam, Depser, Finezol, Fledore, Fluprax, Himzolam, Isorest, Manzolam, Mentolift, Nexlpra, Propnix, Prozam, Selamb, Serex, Setex, Tenfree, Trika, Zeftra, Zoloid, Zopain, Zopic

Similar Products:
Hydrea, Temovate, Coumadin, Propecia, Clarinex, Jorifex, Presovasc, Melwin, Deriva, Nebicard, Cratisone,

Also known as: Alprazolam


Alprose is a benzodiazepine (ben-zoe-dye-AZE-eh-peen). Alprazolam affects chemicals in the brain that may be unbalanced in people with anxiety. Alprose is used to treat anxiety disorders, panic disorders, and anxiety caused by depression.

You should not use Alprose if you have narrow-angle glaucoma, if you also take itraconazole or ketoconazole, or if you are allergic to Alprose or similar medicines (Valium, Ativan, Tranxene, and others).

Alprazolam may be habit-forming. Misuse of habit-forming medicine can cause addiction, overdose, or death.

Do not drink alcohol while taking Alprose. This medication can increase the effects of alcohol. Alprazolam may be habit-forming and should be used only by the person for whom it was prescribed. Keep the medication in a secure place where others cannot get to it.


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


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

Side effects

The most common side effects associated with Alprose 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.


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Solitary versus multiple carcinoid tumors of the ileum: a clinical and pathologic review of 68 cases. We have recently found that isogenic deletion of mgtE leads to increased cytotoxicity through effects on the type III secretion system. The ethiology of acute infectious diarrhea and also biochemical, epidemiological and clinical characteristics of children dying with infectious diarrhea are investigated in this study. Chronic abdominal pain in children: a clinical report of the American Academy of Pediatrics and the North American Society for Pediatric Gastroenterology, Hepatology and Nutrition. We report new epidemiological data on known Type 2 diabetes in the Basque Country. The surgical technique was individualized according to the location of the perforation and the severity of the local inflammatory and necrotic findings. There is a gradual onset of pain with no clear history of injury. p32 interacts with PKC mu in a compartment-specific manner, as it can be coimmunoprecipitated mainly from the particulate and not from the soluble fraction, despite the presence of p32 in both fractions. The protective effects of yi-xin-kang capsule on the structure and function of rat myocardial mitochondria. Evaluation of prognosis and myocardial ischemia using thallium in myocardial tomoscintigraphy.

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Simultaneous occurrence of three squamous cell carcinomas in a recessive dystrophic epidermolysis bullosa patient. Although nuclear transcription factor-kappaB (NF-kappaB) is also activated by ER stress, whether this response depends on IRE1 is unknown. The frequency of post-incisional hernia at one year is similar to that reported with the latter approach. The receding dimension was drawn with parallel or converging lines. A new conception of end-stage lung disease in usual interstitial pneumonia, based on the dying back of the pulmonary acinus, is proposed, which may improve the sensitivity and specificity of the diagnosis and provide an understanding of its pathogenesis. An influence of long-term cyclosporine-A (CyA) therapy on glucose metabolism was analyzed in a group of 122 heart transplant recipients who developed hyperglycemia after heart transplantation. It was found that painless ischemia revealed early in myocardial infarction affects negatively left ventricular systolic and diastolic functions thus strongly suggesting an unfavorable short-term prognosis. THE ACTIVITIES OF SOME ENZYMES OF TRYPTOPHAN METABOLISM IN FETAL, NEONATAL AND ADULT RAT LIVER AND KIDNEY. In addition, the cells in the hypoxia-preconditioning group were found to be in early stages of apoptosis, whereas cells from the hypoxia group were in the later stages of apoptosis. Preventive effect of procainamide in digitalis-induced ventricular ectopic beats.

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Diarylheptanoids 1-3 were found to inhibit lipid peroxidation in a more potent manner than alpha-tocopherol. Membrane signaling by complement C5b-9, the membrane attack complex. Effect of two candidate genes on the Salmonella carrier state in fowl. The TAF-containing form corresponds to the TFIID complex, whereas the form lacking TAFs corresponds to TBP itself or to some other TBP complex. Thus, this study provides both the clues at the protein level for the increase of the two bioactive components upon UV irradiation and the profile of UV-responsive proteins in L. We concluded that the results of limiting dilution studies published thus far must be evaluated with caution. By measuring rates of remodeling at seven different sites on a mononucleosome and at six different sites on the central nucleosome of a trinucleosome, we have found that BRG1 opens centrally located sites more than an order of magnitude better than SNF2h. L-NMMA treatment after completion of resuscitation did not deteriorate gastrointestinal blood flow. Somatic-cell nuclear transfer (SCNT) experiments have paved the way to the field of cellular reprogramming. Antihypertensive efficacy and safety of olmesartan medoxomil compared with amlodipine for mild-to-moderate hypertension.

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Furthermore, we excluded a role for Ofd1 in the pathogenesis of the spontaneous mouse mutant Xpl, which had been proposed as a mouse model for this condition. In this study, systematic experiments were conducted to investigate the influences of PFP vaporization on the morphology and floating ability of hydrogels. Our results suggest that carbonic anhydrase isozymes in type I cells play an important role in chemoreception for hypercapnia. While the pituitary galanin gene is highly responsive to oestrogen stimulation in vivo, in vitro effects of oestrogens on pituitary galanin gene expression have been less studied. Patients received Dx 20 mg m(-2), bleomycin 15 U m(-2) and vincristine 2 mg as a 30-min intravenous infusion each. Etiological factors of bone metabolism disorders in inflammatory bowel diseases have been the subject of interest of many researchers. Gap junctions between murine neurons (also known as electrical synapses) can be composed of connexin 36, connexin 45 or connexin 57 proteins, depending on the type of neuron. Langmuir-Blodgett depositions during lipid film compressions and decompressions were also analyzed by AFM. These results demonstrate a new mechanism of UV radiation immunosuppression whereby UV radiation activates B cells in the skin-DLN that can suppress DC activation of T cell-mediated immunity.

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These considerations could provide better alternatives in the assays chosen as correlates of immunity and may more accurately predict efficacy and assure batch-to-batch consistency. TLR2-TLR4/CD14 polymorphisms and predisposition to severe invasive infections by Neisseria meningitidis and Streptococcus pneumoniae. Maintenance of low histone ubiquitylation by Ubp10 correlates with telomere-proximal Sir2 association and gene silencing. The patient was diabetic, hypertensive and with impaired heart function, aggravated by anemia. The structure is similar to that of Sso10b1 (also called Alba) from the same organism. After an extensive search of the literature, 164 patients treated for fungal hip or knee prosthetic joint infection (PJI) were reviewed.

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Comparison of the clinical characteristics of renal transplant recipients who underwent early versus late graft nephrectomy. Resistance of Mycobacterium tuberculosis to antituberculotic drugs in Czech Republic in 2003. In a murine lung epithelial cell line (MLE-12), the addition of chlorophenylthio-cAMP (cpt-cAMP) causes a 4-fold increase in AQP5 mRNA and protein levels and induces translocation of AQP5 to the apical plasma membrane. Ultimately, functionalized ELPs demonstrate the ability to function as an in vivo hemostatic material over bleeding wounds. Far tails of the density of states in amorphous organic semiconductors. The participants were assessed at baseline before random assignment and 6 and 12 months after surgery. Livers from all the animals subjected to hepatic ischemia showed decreased expression of endothelial nitric oxide synthase, and all but one animal from this group showed expression of the inducible isoform both in inflammatory cells and in hepatocytes. These results reaffirm biaxin dose pediatric TDA-producing Roseobacter bacteria as a promising group to be used as probiotics in aquaculture, whereas Actinobacteria, Pseudoalteromonas, Photobacteriaceae, and Vibrionaceae should be used with caution. In 16 patients with multiple lesions, underwent surgery at bone shaft (29 patients) and bone epiphysis (26).

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The proportion of normal individuals scoring below Z score thresholds drawn from research criteria for HAND, or false-positive frequencies, was estimated in a normal Kenyan population and a simulated normal population using varied interpretations of research criteria for HAND. The ability of the prostacyclin analogue 7-oxo-PGI2 to inhibit infarct size in in vivo rat heart was assessed. iGRASP achieved higher acceleration capability than either parallel imaging or coil-by-coil compressed sensing alone. xFKBP encodes a 63-kDa protein that shares high sequence homology with mouse FKBP65. Thus, ACE inhibitors and ARBs may act by attenuating the deleterious effect of angiotensin II on vasoconstriction side effects of ventolin tablets in pregnancy , fibrosis, inflammation, apoptosis and beta-cell death in the pancreas, thereby protecting a critical beta-cell mass essential for insulin production. The binding epitopes of four mAbs targeting the FVIII C2 domain were mapped with HDX-MS. We used mean weight diameter, normalized enzyme activity (NEA) and carbon gain from straw amendment for addressing soil aggregation, microbial biochemical activity and potential C sequestration, respectively.

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Clinical and laboratory evaluation of streptokinase-streptodornase in oral surgery. The purpose is to viramune storage evaluate the potential of using OSL from components in personal electronic devices such as smart phones as a means of emergency dosimetry in the event of a large-scale radiological incident. Such transient rise and fall expressions of TGase 2 were also found with the sequential amount of RT-PCR products during the same period. The use of physical activity in addition to insulin and/or oral antidiabetic agents and diet is strongly recommended in the treatment of diabetes mellitus. Gestational changes in endothelium-dependent vasorelaxation in human umbilical artery.

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