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Alpram (Alprazolam)

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Alpram 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). Alpram is mostly used to treat anxiety disorders, panic disorders, and nausea due to chemotherapy. Alpram 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:
Acalm, Aldep, Alflux, Alprasan, Alprax, Alprine, Alpron, Alproz, Alwe, Alzac, Alzam, Alzoax, Alzoft, Alzopam, Anxizam, Apsolam, Calmef, Dazolam, Depoxit, Depser, Dipra, Elflu, Esteem, Finezol, Fledore, Hiprazole, Imprax, Mebasap, Meloprax, Niravam, Nokzok, Nucalm, Poize, Pranol, Prozam, Rivcam, Rozin, Somnarest, Suzilam, Tagat, Tenil, Tensyl, Zedel, Zeecam, Zolam, Zolar, Zolorest, Zopax, Zopic, Zotin

Similar Products:
Sustiva, Cardura, Prograf, Lopid, Seroquel, Noroxin, Valsar, Novozithron, Clonix, Bonetuf, Domperal, Cobanerve, Salbomin, Taremis,

Also known as: Alprazolam


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

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


Take Alpram XR exactly as it was prescribed for you. Do not take the medication in larger amounts, or take it for longer than recommended by your doctor. Follow the directions on your prescription label.

Your doctor may occasionally change your dose to make sure you get the best results from this medication.

Alpram XR may be habit-forming and should be used only by the person it was prescribed for. Alpram XR should never be shared with another person, especially someone who has a history of drug abuse or addiction. Keep the medication in a secure place where others cannot get to it. Do not crush, chew, or break a Alpram extended-release tablet. Swallow the tablet whole. It is specially made to release alprazolam slowly in the body. Breaking the tablet would cause too much alprazolam to be released at one time.

Contact your doctor if this medicine seems to stop working as well in treating your panic or anxiety symptoms.

Your symptoms may return when you stop using Alpram XR after using it over a long period of time. You may also have seizures or withdrawal symptoms when you stop using Alpram XR.

Withdrawal symptoms may include blurred vision, trouble concentrating, loss of appetite, diarrhea, muscle twitching, numbness or tingling, or increased sensations.

Do not stop using Alpram XR suddenly without first talking to your doctor. You may need to use less and less before you stop the medication completely.

To be sure this medication is helping your condition, your doctor will need to check your progress on a regular basis. Do not miss any scheduled visits to your doctor.

Store Alpram XR at room temperature away from moisture, heat, and light. Remove any cotton from the bottle of disintegrating tablets, and keep the bottle tightly closed.

Keep track of how many pills have been used from each new bottle of this medicine. Benzodiazepines are drugs of abuse and you should be aware if any person in the household is using this medicine improperly or without a prescription.

Detailed Alpram XR dosage information


Seek emergency medical attention if you think you have used too much of this medicine. An overdose of Alpram 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 at room temperature away from light and moisture. Do not store in the bathroom. Keep all medications away from children and pets.Do not flush medications down the toilet or pour them into a drain unless instructed to do so. Properly discard this product when it is expired or no longer needed. Consult your pharmacist or local waste disposal company for more details.

Side effects

The most common side effects associated with Alpram 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.


You should not take Alpram 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 Alpram 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 Alpram 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.

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

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SelM transcripts were silenced by intramuscular injection with double-stranded RNAs (dsRNAs). Vascular inflammation is an important event in the development of vascular diseases such as tumor progression and atherosclerosis. To identify regulators of intracellular signaling, we targeted 541 kinases and kinase-related molecules with small interfering RNAs (siRNAs), and determined their effects on signaling with a functional proteomics reverse-phase protein array (RPPA) platform assessing 42 phospho and total proteins. This is concerning, given that the adverse effects of many of these conditions can be ameliorated if discovered in a timely fashion. The development of a protocol for biomolecule immobilisation onto a surface plasmon resonance (SPR) sensor surface using inexpensive polythiol compounds is presented here. As a model to test the feasibility of using synthetic genes for gene therapy, we PCR-amplified a fragment containing the CMV promoter, the luciferase gene and a polyadenylation signal.

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Pseudohypertension--a rare or common problem in the treatment of hypertension. Treatment plans of 24 bladder cancer patients referred to radical 4-field conformal radiotherapy were analyzed. Nerve fiber layer thickness in exudative age-related macular degeneration in Japanese patients. New morphological and biochemical information on the cartilaginous tissues in squid, horseshoe crab and amphioxus reveals the presence of CNBr-insoluble, non-collagenous matrix proteins, potentially extending the jawless craniate family of cartilaginous proteins into the invertebrates. Twenty-eight per cent were found to have otitis media and 37 per cent to have malaria. The agonist was administered by subcutaneous injection at an initial dose of 0.05 mg per kilogram of body weight every 4 weeks. Because understanding the modes of actions of these inhibitors and improving their properties will rely on a better understanding of JNK structure, JNK catalytic mechanisms and substrates, recent advances in these areas of JNK biochemistry are also considered. The promise of improved QOL for the HNC patient is attainable through additional research in conjunction with advances in clinical treatments and patient management protocols. Aspirin down-regulates tryptophan degradation in stimulated human peripheral blood mononuclear cells in vitro. Using in vitro actin depolymerization assays, we found that caspase-11 and Aip1 work cooperatively to promote cofilin-mediated actin depolymerization.

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