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Xenotril (Clonazepam)
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Xenotril

Xenotril is a medication used to prevent and treat seizures, panic disorder, and for the movement disorder known as akathisia. It is a tranquilizer of the benzodiazepine class. It is taken by mouth. It begins having an effect within an hour and lasts between six and 12 hours. Xenotril was initially patented in 1964 and went on sale in the United States in 1975. It is available as a generic medication.

Other names for this medication:
Almac, Calmnir, Cleps, Cloam, Clodep, Clonasig, Clotas, Cloze, Clozipam, Deptune, Easyfeel, Ection, Epicloz, Epizam, Escimax, Escitacalm, Escitapax, Escitrac, Estalonix, Jbcloz, Lonazep, Lozep, Meloprax, Melzap, Nexclo, Norep, Nozim, Onapil, Petril, Sezolep, Somnolex, Somnotril, Xitzen, Zeficar, Zepam, Zepamax, Zeptril, Zicam

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Remeron, Phenergan, Vermox, Ilosone, Protonix, Panadol, Priligy, Altace, Lipitor, Anitrim, Doxazosin, Fenadin, Resporito, Artaz, Betanol, Cefadil,

Also known as: Clonazepam

Description

Xenotril is an anti-anxiety medication in the benzodiazepine family, the same family that includes diazepam (Valium), alprazolam (Xanax), lorazepam (Ativan), flurazepam (Dalmane), and others. Xenotril and other benzodiazepines act by enhancing the effects of gamma-aminobutyric acid (GABA) in the brain. GABA is a neurotransmitter (a chemical that nerve cells use to communicate with each other) that inhibits brain activity. It is believed that excessive activity in the brain may lead to anxiety or other psychiatric disorders. Xenotril is primarily used for treating panic disorder and preventing certain types of seizures.

Xenotril is useful alone or as an adjunct in the treatment of the Lennox-Gastaut syndrome (petit mal variant), akinetic and myoclonic seizures. In patients with absence seizures (petit mal) who have failed to respond to succinimides, Xenotril may be useful.

Dosage

Xenotril is also used to treat symptoms of akathisia (restlessness and a need for constant movement) that may occur as a side effect of treatment with antipsychotic medications (medications for mental illness) and to treat acute catatonic reactions (state in which a person does not move or speak at all or moves or speaks abnormally). Talk to your doctor about the possible risks of using this medication for your condition.

This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.

Keep all appointments with your doctor and the laboratory. Your doctor will order certain lab tests to check your response to Xenotril.

Do not let anyone else take your medication. Xenotril is a controlled substance. Prescriptions may be refilled only a limited number of times; ask your pharmacist if you have any questions.

It is important for you to keep a written list of all of the prescription and nonprescription (over-the-counter) medicines you are taking, as well as any products such as vitamins, minerals, or other dietary supplements. You should bring this list with you each time you visit a doctor or if you are admitted to a hospital. It is also important information to carry with you in case of emergencies.

Overdose

Treatment after Overdose. If a person accidentally overdoses on Xanax, Valium, or Xenotril due to interactions with prescription medications, this is unlikely a sign of addiction or abuse. However, if the overdose was the result of benzodiazepine abuse of any kind, help is needed.

Storage

Store at 25 degrees C (77 degrees F); excursions permitted to 15 to 30 degrees C (59 to 86 degrees F).

Side effects

The most common side effects associated with Xenotril 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

There are no adequate studies in women for determining infant risk when using this medication during breastfeeding. Weigh the potential benefits against the potential risks before taking this medication while breastfeeding.

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The role of AHI1 and CDKN1C in cutaneous T-cell lymphoma progression. Clinical utility and cost saving of a 7 day per week ET for management of patients with suspected and/or known coronary artery disease utilizing ECGT was assessed after adequate training. We hypothesized that RYGB reverses NASH and fibrosis, and indocyanine green (ICG) clearance provides a sensitive measure for detecting asymptomatic fatty liver disease. The aim of this study was to investigate sleep and the sleep modulating effect of 1-desamino-8-D-arginine vasopressin (DDAVP) in patients with primary monosymptomatic nocturnal enuresis and controls by means of both conventional polysomnography and computerized electroencephalographic (EEG) power analysis. The influence of these shape differences was also observed for unfamiliar shapes, demonstrating that the influence of categorization experience was not modulated by the retrieval of shape features from known categories but rather related to a different perception of shape by age. Over time, we observed more visits in our pediatric emergency department with length-of-stay (LOS) of more than 10 hours, whereas our mean LOS was approximately 3 hours. The results indicate that selected halotolerant and halophilic species synthesize specific bioactive metabolites under conditions that represent stress for non-adapted species. Based on these adjuvant mechanisms, we developed iNKT cell-targeted adjuvant therapy and carried out a phase I/IIa trial on advanced lung cancer patients. Klebsiella pneumoniae is a member of the family Enterobacteriaceae, opportunistic pathogens that are among the eight most prevalent infectious agents in hospitals.

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