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Anxofit (Alprazolam)

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Anxofit 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). Anxofit is mostly used to treat anxiety disorders, panic disorders, and nausea due to chemotherapy. Anxofit 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:
Alpram, Alprax, Alprine, Alprosym, Alprozam, Alwe, Alzoact, Alzot, Anzocalm, Dazolam, Depten, Dipra, Emlol, Flumusa, Fluprax, Mebasap, Morecalm, Oclam, Riolam, Rivcam, Sanprazole, Sinozol, Sinzolam, Synozolam, Tancalm, Tenfree, Xerodep, Zenax, Zolin, Zolorest, Zopax

Similar Products:
Biaxin, Nolvadex, Pamelor, Chloromycetin, Zovirax

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.


Take Anxofit exactly as prescribed by your doctor. Follow all directions on your prescription label. Never use Anxofit in larger amounts, or for longer than prescribed. Tell your doctor if the medicine seems to stop working as well in treating your symptoms.

Anxofit may be habit-forming. Never share Anxofit with another person, especially someone with a history of drug abuse or addiction. Keep the medication in a place where others cannot get to it.

Misuse of habit-forming medicine can cause addiction, overdose, or death. Selling or giving away this medicine is against the law.

Do not crush, chew, or break a Anxofit extended-release tablet. Swallow the tablet whole. Call your doctor if this medicine seems to stop working as well in treating your panic or anxiety symptoms. Do not stop using Anxofit suddenly, or you could have unpleasant withdrawal symptoms. Ask your doctor how to safely stop using this medicine.


Seek emergency medical attention if you think you have used too much of this medicine. An overdose of Anxofit 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 Anxofit dosage information

Side effects

The most common side effects associated with Anxofit 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.


Appropriate studies performed to date have not demonstrated geriatric-specific problems that would limit the usefulness of alprazolam in the elderly. However, elderly patients are more likely to have unwanted effects (eg, severe drowsiness, dizziness, confusion, clumsiness, or unsteadiness) and kidney, liver, or lung problems, which may require caution and an adjustment in the dose for patients receiving this medicine.

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Comparison of the monoamine oxidase inhibiting properties of two reversible and selective monoamine oxidase-A inhibitors moclobemide and toloxatone, and assessment of their effect on psychometric performance in healthy subjects. These combined results indicate that inhibition of ABL activity is reversible and suggest that a cellular component interacts noncovalently with ABL to inhibit its autophosphorylation. However, the comorbidity and the histopathologic correlation of psoriasis and mycosis fungoides (MF) have been less studied. Chemical ionization mass spectra of L-methionine and L-methionine analogs. Vigabatrin versus ACTH as first-line treatment for infantile spasms: a randomized, prospective study. VirtuaLinac, a cloud based web application utilizing Geant4 Monte Carlo code, was used to model the Linac treatment head components.

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Modification of the fluorescent allergosorbent test as an inhibition assay for determination of cross-reactivity among aeroallergens. Several of the physicochemical and conformational factors influencing duplex stabilization are analyzed with respect to their relative importance for the antisense field. A series of silica materials with ordered cagelike (SBA-16 mesostructure) and disordered (SiO2-gel) porosities and varying pore sizes were employed as catalyst supports. No differences in variables were noted for women who viewed God as more or less angry. Lessons learned specific to this platform are outlined, as well as the more general issues of delivering Emergency Medicine in the maritime environment. Here, we evaluated the role of TFPI-2, a Kunitz-type serine protease inhibitor, which has been previously described as a tumor suppressor gene in several types of cancer, including glioma. Implant growth was monitored and at 3 months postimplantation grafts were recovered.

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Fetal and maternal lipoprotein metabolism in human pregnancy complicated by type I diabetes mellitus. Pressors for cardiopulmonary resuscitation: is there a new kid on the block?. Emerging HFRs including hexabromobenzene, Dechlorane 604 Component B, and Dechlorane plus (DP) isomers also were sampled by the PUF-based PAS. The ultimate reactive metabolite is evidently the same as that formed with liver microsomes and NADPH since the glutathione conjugates were apparently identical. Larger well-designed trials are needed to enable safe conclusions. Immunoglobulins of bursectomized chickens in immunoelectrophoresis (IE). All of the enzymes degraded protein II, but this susceptibility appeared to be influenced in part by the species of protein I present.

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300 bp) were found to share a higher degree of homology than those of the tet(O) and tet(M) ORFs themselves. Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants. Formation of a filterable form of the causative agent of tuberculosis in the chemotherapy process (an experimental study). The stress-producing device and its associated protocol are shown to be suitable for investigating the behaviour of cells, cultured on biomaterials subjected to mechanical strain. Chronic exposure to ethanol does result in both brain and behavior dysfunction in male and female rats. When all control mice developed externally palpable tumors, the experiment was terminated, and pancreatic weights compared between control and treated groups. This study provides a mechanistic interpretation for utilization of copper chelators in cancer treatment. All other surgical procedures and postoperative medication were standardized. There is strong evidence from preclinical models for the importance of cytokine-driven pathways in late radiation damage and growing evidence in humans for their relevance to radiation-induced disease.

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The molecular pathways mediating the pathophysiological events in GBS infection are not fully delineated. The sequential changes in community composition during different developmental stages were examined by denaturing gradient gel electrophoresis (DGGE) of polymerase chain reaction (PCR)-amplified 16S rRNA gene fragments in conjugation with sequencing and phylogenetic analysis. Enhancement of fracture healing with parathyroid hormone: preclinical studies and potential clinical applications. This approach enabled the identification of new bioactive components in BR fruits and demonstrates the utility of the method for assessing chemopreventive compounds in foods and food products. A new SHV-derived extended-spectrum beta-lactamase (SHV-24) conferring high-level resistance to ceftazidime but not cefotaxime and cefazolin was identified in Japan. This method allows a check of the whole dosimetry chain for this type of brachytherapy afterloading system and can easily be performed by mail to any institution in the European area and elsewhere. Furthermore, shikonin suppressed VEGF-induced tube formation of HUVECs and CD34 expression in the skin of IL-17 stimulated mice. Maternal IL-1beta pretreatment upregulated ERK and upstream MEK expression at both 61 and 68D gestation, albeit being much more pronounced at 61D gestation. The treatment of periodontal disease based on recent advances in research.

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