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Anilam (Alprazolam)
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Anilam

Anilam 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:
Alfresh, Alltop, Alprazolam, Alprine, Alprowon, Alproz, Alzokam, Alzonex, Apsolam, Benzax, Depwell, Exiten, Notence, Notens, Omelam, Poize, Prozolam, Resta, Resto, Samitol, Tagat, Tensyn, Zolam, Zolark, Zolorel

Similar Products:
Hytrin, Tofranil, Aceon, Combivent, Risperdal, Aldara, Soma, Furadantin, Sporanox, Ovral, Postpon, Sertamax, Pantakure, Ibumol, Obilix,

Also known as: Alprazolam

Description

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

You should not use Anilam if you have narrow-angle glaucoma, if you also take itraconazole or ketoconazole, or if you are allergic to Anilam 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 Anilam. 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.

Dosage

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 Anilam dosage information

Overdose

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

Side effects

The most common side effects associated with Anilam 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

You should not take Anilam if:

you also take itraconazole or ketoconazole (antifungal medicines); or you have a history of allergic reaction to any benzodiazepine (alprazolam, diazepam, lorazepam, Ativan, Klonopin, Restoril, Tranxene, Valium, Versed, and others).

To make sure Anilam is safe for you, tell your doctor if you have ever had:

breathing problems such as COPD (chronic obstructive pulmonary disease) or sleep apnea (breathing that stops during sleep); drug or alcohol addiction; depression, mood problems, or suicidal thoughts or behavior; or kidney or liver disease (especially alcoholic liver disease).

Tell your doctor if you are pregnant or plan to become pregnant. Alprazolam may harm an unborn baby. Avoid taking this medicine during the first trimester of pregnancy.

If you use Anilam while you are pregnant, your baby could become dependent on the drug. This can cause life-threatening withdrawal symptoms in the baby after it is born. Babies born dependent on habit-forming medicine may need medical treatment for several weeks.

You should not breastfeed while using alprazolam.

Anilam is not approved for use by anyone younger than 18 years old.

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Experimental schistosomiasis in the mouse: histogenesis of the schistomiasic granuloma. Unfortunately, rear end crashes are also the most common type of crash at urban signalized intersections, where the majority of crashes occur in British Columbia, Canada. Such differences have implications for design and evaluation of hand tools for the Nigerian female population. Noncontact laser microdissection and catapulting for pure sample capture. Involvement of renin-angiotensin system in the reduced pressure natriuresis response of hyperthyroid rats. EGF and Bcl-x(L) activate the mitogen-activated protein kinase/ERK pathway resulting in upregulation of vascular endothelial growth factor (VEGF), a known inducer of Bcl-2 in endothelial cells. The pH optimum of the enzymes from both sources was 8.4 in either Tris-HCl or barbital buffer. According to a lexical-access hypothesis, priming on verbal-completion tests requires previous access to higher-order nodes such as morphemes or words. Noninvasive physiological assessment of vascular wall sclerosis using carotid pulse tracing and cine magnetic resonance. The role of reactive oxygen species (ROS) in AFB1-induced cell injury was investigated using cultured rat hepatocytes.

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Requirements in preterm infants are increased due to accelerated growth and limited body stores. A novel orphan G-protein-coupled receptor named GPRv53 was obtained through a search of the human genomic DNA data base and analyzed by rapid amplification of cDNA ends (RACE). NUTRITION DISORDERS, DYSPEPSIA AND DISEASES OF THE UPPER RESPIRATORY TRACT IN INFANTS AND SMALL CHILDREN. Regulatory effects of ninjurin-1 on adhesion of myeloid cells in the retina at the early stage of diabetic rats. Treatment possibilities for clinically localised prostate cancer include radical prostatectomy (RP), external beam radiotherapy, brachytherapy, focal therapy and active surveillance. Increased expression of the alpha1 subunit inversely correlated with cell cycle progression and paralleled the expression of p27Kip1 and alpha-smooth muscle actin, as well as the cell size in MCs. Our analysis showed a significant association between appropriate and inappropriate ICD shocks and mortality, with a stronger association for appropriate shocks. Observations based on fluorescence recovery after photobleaching showed that SLBs on the prepared grating supports had some fluidity, while SLBs on the planar support had no fluidity. However, certain differences were observed which also suggest unique pathways associated with the end-stage of aseptic loosening in THA and TKA.

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Sleep arousal response to experimental thermal stimulation during sleep in human subjects free of pain and sleep problems. In the presence of thiols, e.g., glutathione (GSH), formation of 4-(dimethylamino)-2-(glutathion-S-yl)phenol (2-GS-DMAP), 4-(dimethylamino)-2,6-bis(glutathion-S-yl)phenol (2,6-bis-GS-DMAP), and 4-(dimethylamino)-2,3,6-tris(glutathion-S-yl)phenol (2,3,6-tris-GS-DMAP) was observed. Evaluation of less invasive method for saphenous vein harvest in patients with type II diabetes. Peripheral primitive neuroectodermal tumor of the parotid gland region: report of a case with fine-needle aspiration findings. Comparison of the redox bioassay with other assays for luteinizing hormone.

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