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Alrif (Alprazolam)
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Alrif

Alrif 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). Alrif is mostly used to treat anxiety disorders, panic disorders, and nausea due to chemotherapy. Alrif 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:
Aldip, Alfresh, Alpam, Alpkair, Alprazan, Alzocum, Anxyl, Coolam, Cqlam, Depoxit, Depsolam, Depten, Fluprax, Indolam, Jolistar, Mebaspa, Plaxid, Poize, Propnix, Rescalm, Samrox, Somaspas, Suzilam, Welnorm, Wycalm, Zodia, Zoldac, Zolent, Zomark

Similar Products:
Eldepryl, Casodex, Arcoxia, Anafranil, Amethopterin, Azulfidine, Neurontin, Estrace, Addyi, Retin, Kitnil, Attentrol, Mebrin, Baycip, Valpresan, Citraclor,

Also known as: Alprazolam

Description

Alrif 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.

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

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

Dosage

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

Alrif may be habit-forming. Never share Alrif 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 Alrif 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 Alrif suddenly, or you could have unpleasant withdrawal symptoms. Ask your doctor how to safely stop using this medicine.

Overdose

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.

Storage

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 Alrif dosage information

Side effects

The most common side effects associated with Alrif 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.

Contraindications

Tell your doctor if you have ever had any unusual or allergic reaction to this medicine or any other medicines. Also tell your health care professional if you have any other types of allergies, such as to foods, dyes, preservatives, or animals. For non-prescription products, read the label or package ingredients carefully.

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Improving the outcome of patients with castration-resistant prostate cancer through rational drug development. Indicator adjustment to seasonal variation and other significant covariates reduces bias and improves precision. A series of 4-aryl substituted 7-hydroxy-flavones were prepared using the three-step Baker-Venkataraman synthesis in good overall yields. Low oxygen tension stimulates collagen synthesis and COL1A1 transcription through the action of TGF-beta1. For this reason, CRGO was employed for the electrochemical detection of quinine in commercial tonic drink samples, showing high sensitivity and selectivity, and therefore representing a valid low-cost alternative to more complicated and time consuming traditional analytical methods. Whereas stress onset is accompanied by rapid growth inhibition leading to smaller organs, growth will recover and adapt once the stress conditions become stable and do no threaten plant survival. Renal parenchymal oxygenation and hypoxia adaptation in acute kidney injury. Pathological CNS autoimmune disease triggered by traumatic spinal cord injury: implications for autoimmune vaccine therapy. Treatment with DNMT inhibitors increased TGF-beta pathway activity. We undertook a meta-analysis of randomized controlled trials to investigate whether probiotic use during pregnancy and early life decreases the incidence of atopic dermatitis and immunoglobulin E (IgE)-associated atopic dermatitis in infants and young children.

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Research has, therefore, been directed towards finding smaller peptide mimetics that produce similar results to apoA-I, but that are easier to manufacture and administer. Hypoxic-ischemic encephalopathy (HIE) is one of the leading causes of morbidity and mortality in neonates. Preoperative and postoperative data are recorded in a standardized form in order to facilitate their analysis. Our findings suggest that thioneins, either as apoproteins or when complexed as Cd,Zn-MT, Zn-MT, or Cd-MT, are capable of inducing lymphocyte proliferation. It was shown that mosquitoes do not discriminate between sugar solutions with or without these bacteria indicating that sugar-feeding is a possible means to introduce bacteria into mosquitoes. Although MR imaging is in general somewhat more sensitive to the detection of cranial tuberculosis, CT is the diagnostic imaging mainstay in many clinical settings to demonstrate the various aspects of cranial tuberculosis on initial presentation and to monitor the evolution of the disease and response to therapy. Advantages and limitations of diuretic therapy in essential hypertension. To present an updated discussion of those aspects of controlled positive pressure breathing and retained spontaneous regulation of breathing that impact the management of patients whose tissue oxygenation is compromised by acute lung injury.

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Pressurized liquid extraction as a sample preparation method for the analysis of isoflavones in pulses. ODNs containing O(6)-pobG and O (6)-CMG were found to be good substrates for the S. Patients who required SVC intervention were divided into two subgroups-balloon dilation (Group A) and stent implantation (Group B). Potent, orally active heterocycle-based combretastatin A-4 analogues: synthesis, structure-activity relationship, pharmacokinetics, and in vivo antitumor activity evaluation. Secondary outcomes were correlation of pre-LT AFP with vascular invasion and grade of tumour differentiation. High prevalence of muscular ventricular septal defect in neonates. Using an established in vivo model of vascular injury, we investigated the effect of the HMG-CoA reductase inhibitor rosuvastatin on MMP-9 expression and neointima formation. Patients who have undergone gastrectomy had their medical records reviewed for demographic data, type of gastrectomy, short term morbidity, and length of hospital stay.

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I: Strain differences and empirical association with relative chromosome size. Decreased content of reduced and oxidized nicotinamide-adenine dinucleotide phosphate in rat hepatomas. Distribution quantification on dermoscopy images for computer-assisted diagnosis of cutaneous melanomas. Based on the results, the quantities of stain required to detect each marker were determined. The spectroscopic investigations were carried out principally with the octaacetyl derivative of landomycin A, which is more soluble in organic solvents than landomycin A itself. Using the first method, the release rate of the drug was significantly reduced compared with other delivery systems. Mice and lambs were infected with the LI/I, LI/31 or MA54 strain of louping ill virus (LIV) to provide information relevant to testing the efficacy and biosafety of a new generation of flavivirus vaccines based on a Semliki Forest virus (SFV) vector. Ubiquitin C-terminal hydrolase 1 (UCHL1) and the phosphorylated axonal forms of neurofilament H (pNF-H) are markers of brain injury in foals with NHIE.

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