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Alparazole (Alprazolam)
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Alparazole

Alparazole 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:
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Similar Products:
Calan, Lopid, Evista, Luvox, Exelon, Zyvox, Droxol, Ostriol, Coveram, Albazole, Alcicalm, Normolip, Morazin, Tramed, Ibulite,

Also known as: Alprazolam

Description

Alparazole (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.

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

Alparazole 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 Alparazole 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.

Dosage

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

Overdose

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

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 Alparazole XR dosage information

Side effects

The most common side effects associated with Alparazole 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

Do not drink alcohol while taking Alparazole XR. This medication can increase the effects of alcohol. Alparazole XR can cause side effects that may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be awake and alert.

Grapefruit and grapefruit juice may interact with Alparazole XR and lead to potentially dangerous effects. Discuss the use of grapefruit products with your doctor. Do not increase or decrease the amount of grapefruit products in your diet without first talking to your doctor.

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Effect of age and strain on working memory in mice as measured by win-shift paradigm. On-column synthesis coupled to affinity capillary electrophoresis for the determination of binding constants of peptides to glycopeptide antibiotics. Diagnostic pathways in acute pulmonary embolism: recommendations of the PIOPED II investigators. Functional significance of an ossified mandibular symphysis: a reply. Surface chemistry: a non-negligible parameter in determining optical properties of small colloidal metal nanoparticles. Rapid loss of IgM expression by normal murine B cells undergoing IgG1 and IgE class switching after in vivo immunization. Non alcoholic fatty liver disease (NAFLD) is associated to diabetes mellitus, obesity, disturbances in serum lipid levels, insulin resistance and metabolic syndrome. Lectin-mediated targeting and delivery exploits unique surface carbohydrates on mucosal epithelial cells. The microflora also influence the degradation of mucin, the conversion of urobilin to urobilinogen, of cholesterol to coprostanol, and the production of short chain fatty acids.

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Effects of ioversol were compared with equi-iodine doses of iothalamate when applied to cultured bovine aortic endothelial cells or injected into normal rats and rats preconditioned by uninephrectomy, salt depletion, and indomethacin (USIC) to develop radiocontrast nephropathy. The results thus demonstrate considerable regional heterogeneity of astrocytic maturation. The nature of AGE formation and RAGE signaling bring forward possibilities for therapeutic intervention. Sometimes, a patient seeking a solution for rejuvenation of the upper third of the face may present other problems such as a forehead lesion. Mean times to recovery for each anastomotic site were calculated and found to correlate with recovery times, with an R(2) value of 0.86. Analysis of macrocomponents and fatty acids in the market basket of male adolescents in The Netherlands. In addition, actual data from normal subjects as to the 24-hour urinary values for norepinephrine, normetanephrine, vanillylmandelic acid, and 3-methoxy-4-hydroxyphenylglycol were analyzed using path analysis. wt 81 000 (NHCP1), 39 000 (NHCP2) and 21 000, 35 000, 37 000 (NHCP1), 70 000, 112 000, 141 000, 157 000 (NHCP2), 30 000-33 000 (NHCP3) were associated only with the nuclease-sensitive part of chromatin of hepatoma and normal tissue, respectively. The purpose of this study was to assess the surface free energy of a series of composite resin restorative materials, utilizing the concept of critical surface tension (yc).

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Perpetrators of domestic homicide without suicide were significantly younger, had a poorer educational background and were rather foreigners. Osteopontin expression in normal and hypobaric hypoxia-exposed rats. Clinical characteristics of hepatic sinusoidal obstruction syndrome: analysis of 8 cases. bridging the gap: Australian aboriginals and primary health care. The one- and two-electron oxidation of the MTPPs leads to symmetry-breaking of the metal-porphyrin core, resulting in a large beta value that is perhaps aided in part by contributions from the two-photon resonance enhancement. Stewardship of APhA officers--in advancing the profession and public health.

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Heart regeneration is well documented in amphibia and fish and in developing mammals. This article intends to show possibilities and examples of actual use of ICIDH in rehabilitation. Although having sufficient placements can be challenging for university programmes, ensuring that the experiences provided are of high quality is also important and requires significant attention by university academics and practice education staff, practice educators, managers and practice organisations alike. The purpose of this study is to investigate the fundamental property of the superior head of the lateral pterygoid muscle (LPT) of the human beings. Moreover, they were shown to be an active substrate for surface-enhanced Raman scattering measurements. Unexpectedly, the COX-1 inhibitor SC 58560 also reduced dynorphin A(2-17)-induced, but not NMDA-induced, release of prostaglandin E2.

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Chromosomal location, cloning and nucleotide sequence of the Bacillus subtilis cdd gene encoding cytidine/deoxycytidine deaminase. A vertical sectional survey on 193 children aged 7 - 11 years was performed in 1996. The patient underwent right inguinal orchiectomy and was diagnosed with nonseminomatous germ cell tumor of the right testis, composed of yolk sac tumor, teratoma, and embryonal carcinoma with no evidence of metastatic disease. Trichloroethylene cranial neuropathy: is it really a toxic neuropathy or does it activate latent herpes virus?. A typical feature in this area, different from the overall situation in the Federal Republic of Germany as a whole, is the larger group of homosexuals among the AIDS patients and a higher percentage of intravenous drug-dependents among the HIV-infected subjects. Oxaprotiline significantly resembled amitriptyline in its antidepressant potential. Diverticular disease is a common entity in the USA with an apparent increasing incidence worldwide. Cardiac resynchronisation may reduce all-cause mortality: meta-analysis of preliminary COMPANION data with CONTAK-CD, InSync ICD, MIRACLE and MUSTIC. The results indicate that I-J is a novel dimeric surface molecule, most likely to be a homodimer, expressed on T cells according to the major histocompatibility complex. The remaining subfamilies, V delta 3, V delta 4, V delta 5, and V delta 6, were only represented by one clone each.

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An image of a resolution chart through a solution of latex microspheres with an attenuation of 22 mean free paths is obtained with a resolution of 20 mum. Selective depletion with antibodies showed that killer cells stimulated by combination chemoimmunotherapy treatment bear phenotypic characteristics of asialo-GM1-positive cells. Disconnecting the Golgi ribbon from the centrosome prevents directional cell migration and ciliogenesis. Each stage of CRC progression is characterized by a particular genetic profile, and both carcinomatoses and liver metastases are more genetically complex than local recurrences and primary carcinomas. This device has also been successfully investigated as a self-temperature-compensated in situ uniaxial strain sensor without any angular dependence and with high accuracy in recovery analysis, leading us to expect many industrial applications. It has the potential to enrich current approaches to city planning and replace traditional top-down strategies with realistic city plans that benefit all city dwellers.

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We determined that the mutant protein with deletion of the periluminal region of the transmembrane domain (Thr-32 to Ile-21) was translocated into microsomes and localized on the inner surface of the microsomal membrane in a fashion identical to that of the parental TNF. In combination with morphological and other data, this abundance of genomic information will have a broad range of applications, including not only helping conservation biologists understand ecosystem biodiversity, but also understanding the evolutionary histories of organisms, mending damaged landscapes, and investigating interactions of plants with pollinators and pests. Moreover, the E- or Z-stereochemistry of the double bond in fulvene products can be easily controlled by performing the reaction in different solvents. In the proband and in the mother a G3341A mutation was also detected in exon 17, which causes an R1070Q amino acid change. It is demonstrated that during apoptosis, ROS burst acted as an early event followed by depolarization of MMP, prolonged ROS generation, and significantly declined GSH level. We calculated odds ratios to determine whether control in year 1 or prilosec otc dosage in year 2 predicted control in Years 3-6. Air pollution and respiratory disease in a tropical urban setting in Cotonou, Benin. At various times after injection, serum and gut, nasal and bronchoalveolar lavage samples were collected. Motions in the right and left hemidiaphragms changed with posture. Analysis of factors involved in determining urinary bladder voiding cycle in urethan-anesthetized rats.

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An assay system comprising 5 spots containing starch and potassium iodide on filter paper incorporating or without capsaicin and a coloring reagent was designed. A clone (FDP 14) was selected that produces monoclonal antibodies (MoAbs) of the IgG1 kappa type that react with a neoantigenic determinant exposed in these XDPs, but not in intact fibrinogen or in fibrin monomers. These findings suggest that marching band can help to meet current physical activity recommendations when measured in steps-per-day using a pedometer. The progesterone receptor stimulates cell-free transcription by enhancing the formation of a stable preinitiation complex. The 9 S ligand-free or ligand-bound glucocorticoid receptor was converted to the monomeric 4-5 S form upon exposure to 0.4 M NaCl even in the presence of the stabilizing agent molybdate.

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