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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:
Aderta, Albiz, Aleez, Alflux, Alpraquil, Alprawin, Alprogard, Alproz, Alsert, Alzokam, Anxicalm, Anxigon, Anxofit, Cooltime, Cqlam, Dazolam, Depser, Ezoprax, Fledore, Flunix, Fluxin, Himzolam, Hipose, Hiprazole, Indolam, Kaprolam, Oclam, Parazolam, Pecalm, Prazolam, Proprazolam, Prozam, Resto, Restyl, Somnirest, Zolin, Zopam

Similar Products:
Keflex, Sovaldi, Trandate, Avodart, Silagra, Minocin, Bystolic, Roglin, Orchidol, Lekoklar, Luvle, Heligo,

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

Take this medication by mouth as directed by your doctor. Dosage is based on your medical condition, age, and response to treatment. Your dose may be gradually increased until the drug starts working well. Follow your doctor's instructions closely to reduce the risk of side effects.This medication may cause withdrawal reactions, especially if it has been used regularly for a long time or in high doses. In such cases, withdrawal symptoms (such as seizures) may occur if you suddenly stop using this medication. To prevent withdrawal reactions, your doctor may reduce your dose gradually. Report any withdrawal reactions immediately.Along with its benefits, this medication may rarely cause abnormal drug-seeking behavior (addiction). This risk may be increased if you have abused alcohol or drugs in the past. Take this medication exactly as prescribed to lessen the risk of addiction.When this medication is used for a long time, it may not work as well. Talk with your doctor if this medication stops working well.Tell your doctor if your condition persists or worsens.

Overdose

Seek emergency medical attention if you think you have used too much of this medicine. An overdose of Anilam XR can be fatal.

Overdose symptoms may include extreme drowsiness, confusion, muscle weakness, loss of balance or coordination, feeling light-headed, fainting, and coma.

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 XR 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

In deciding to use a medicine, the risks of taking the medicine must be weighed against the good it will do. This is a decision you and your doctor will make. For this medicine, the following should be considered:

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All patients referred because of exudative AMD in one eye during an 18-month period were included in the study group. Because Bim(-/-) mice develop spontaneous systemic autoimmunity, we investigated whether Bim(-/-) DCs contributed to lymphoproliferation and autoimmunity in these mice. Next, comedones were sampled again from the same patients and classified into five groups: microcomedo (MC), noninflammatory open comedo (NIOC), noninflammatory closed comedo (NICC), inflammatory open comedo (IOC), and inflammatory closed comedo (ICC). Attempts to detect either sterol in hexane extracts of marine bay water have not been successful because of the interference of other lipid-like material. Furthermore, blockade of the V(1b) receptor or the CRF1 receptor may be useful in treating subjects suffering from chronic stressful conditions. JNK1 physically interacted with E2F1 and inactivated it via direct phosphorylation. This is because spine MRI lesion often retrieved in SpA are sumycin 500 mg price in uae not very specific, and can be found in many other diseases such as malignancy and osteoarthritis. One member of a gro-ESL-like chaperonin multigene family in Bradyrhizobium japonicum is co-regulated with symbiotic nitrogen fixation genes. By screening through all cortically expressed miRNAs in HeLa cells, we show that several members of the miR-34/449 family control mitotic duration and spindle rotation. As the cases where sensorineural deafness disappeared within six months after head injury were rare, final evaluation of the hearing loss can be made one year after the head injury.

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Electroconvulsive therapy for psychosis in a patient with epilepsy related to hypothalamic hamartoma. Metabolic differences were observed in total CYP oxidative metabolism (7-ethoxycoumarin O-deethylation, total testosterone hydroxylation), as well as in CYP3A4, CYP2C9 or CYP2C19 activities (testosterone oxidations at 6beta-, 16beta- and 17-positions, respectively). Structure and antiviral activity of adamantane-containing polymer preparation. Canfosfamide HCl (CAN) is a glutathione analogue prodrug that is activated by glutathione S-transferase P1-1 and induces apoptosis. pasteurii for strengthening brick masonry civil engineering structures. Taken together, these results suggest that both T3 and TRE binding are important determinants of the formation of specific TR complexes in solution and on DNA.

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The evolving role of telomerase inhibitors in the treatment of cancer. Toll-like receptor (TLR)4 has recently been shown to reside in the Golgi apparatus of intestinal crypt epithelial m-ICcl2 cells, colocalizing with internalized lipopolysaccharide (LPS). If resection cannot be carried out, a unilateral intrahepatic cholangioenteric anastomosis with preference for the round ligament technique is an excellent procedure when properly applied. Steroid hormones and hypertension: the cortisol-cortisone shuttle. In both strains, CYP6Z1 expression is higher in males than females. Secondary outcomes were risk of candidiasis/aspergillosis, risk of IFI mortality and risk of all-cause mortality. Here, we demonstrate CSD in the solitary Cotesia vestalis, using microsatellite markers. Specifically, we test if the species expresses a geographically unstructured, or generalist, phenotype throughout its range or if it shows geographically localized morphological differentiation across disparate environments. This review will give a brief overview of our current knowledge of TLR biology, and will focus on TLRs as key components in complex networks that activate, integrate and select the appropriate innate and adaptive immune responses in the face of immunological danger.

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