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Adnil (Clonazepam)

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Adnil is used to prevent and control seizures. This medication is known as an anticonvulsant or antiepileptic drug. It is also used to treat panic attacks. Adnil works by calming your brain and nerves. It belongs to a class of drugs called benzodiazepines.

Other names for this medication:
Adnil, Almac, Anxrea, Azpax, Calmnir, Cleps, Clodep, Clonapax, Clonapik, Clonasig, Clonaxyl, Clonazepam, Clonix, Clonoasig, Clonopam, Clonotril, Closis, Clotas, Clotweet, Cloze, Clozorix, Dipwell, Eminaz, Epicloz, Epitril, Escimax, Escitacalm, Escitapax, Escitrac, Esitor, Ezinite, Jasoclam, Klopam, Lonipax, Lozep, Meloprax, Nazee, Nozim, Onapil, Ozepam, Prasilife, Rivotril, Sezolep, Somnolex, Xenotril, Xitzen, Zepam, Zicam, Zozep

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Also known as: Clonazepam


Adnil is a benzodiazepine medication that was initially primarily used for the treatment of seizures occurring in epilepsy and for anxiety, specifically anxiety that occurs in panic disorder. Adnil is available in tablet form (0.5 mg, 1 mg, 2 mg) and as disintegrating wafers that are taken orally.

While Adnil is generally prescribed for the treatment of anxiety disorders, such as panic disorder, and seizure control, it is intended as a short-term treatment protocol as opposed to a long-term treatment solution due to issues with tolerance (see below). In addition to treating anxiety and seizures, Adnil has also been used in the treatment of:

chizophrenia, especially when the individual with schizophrenia has a restless or irritable component and is not responding to antipsychotic medications.

The manic phase of bipolar disorder or for restlessness associated with depression in bipolar disorder.

Tic disorders, such as Tourette's syndrome, by acting as a muscle relaxant and producing sedation.

Restless leg syndrome.

Withdrawal from alcohol or treatment for other substance abuse or addiction issues.

Adnil has a relatively slow onset of action (it takes a while for the drug to begin working) and a half-life of between 10 and 50 hours. As it has a relatively slow onset of action and is a longer-acting benzodiazepine, Adnil is more suited for the treatment of anxiety, seizures, and other similar disorders as opposed to being a useful sleep aid, even though it is sometimes prescribed for that purpose. Sleep aids need to work quickly, whereas with Adnil, a person takes the drug early in the day and doesn't have to worry about monitoring for signs of a seizure or panic attack as it stays in the system a relatively long time. Its effects last longer than those of shorter-acting benzodiazepines, such as Xanax.

As it is a Schedule IV controlled substance, Adnil can only be legally acquired with a prescription from a physician.


Your doctor will probably start you on a low dose of Adnil and gradually increase your dose, not more often than once every 3 days.

Adnil can be habit-forming. Do not take a larger dose, take it more often, or take it for a longer period of time or in a different way than prescribed by your doctor. Take Adnil exactly as directed. Do not take more or less of it or take it more often than prescribed by your doctor.

Adnil may help control your condition, but will not cure it. It may take a few weeks or longer before you feel the full benefit of Adnil. Continue to take Adnil even if you feel well. Do not stop taking Adnil without talking to your doctor, even if you experience side effects such as unusual changes in behavior or mood, If you suddenly stop taking Adnil, you may experience withdrawal symptoms such as new or worsening seizures, hallucinating (seeing things or hearing voices that do not exist), changes in behavior, sweating, uncontrollable shaking of a part of your body, stomach or muscle cramps, anxiety, or difficulty falling asleep or staying asleep. Your doctor will probably decrease your dose gradually.


Symptoms of clonazepam overdosage, like those produced by other CNS depressants, include somnolence, confusion, coma and diminished reflexes.

Treatment includes monitoring of respiration, pulse and blood pressure, general supportive measures and immediate gastric lavage. Intravenous fluids should be administered and an adequate airway maintained. Hypotension may be combated by the use of levarterenol or metaraminol. Dialysis is of no known value.

Flumazenil, a specific benzodiazepine-receptor antagonist, is indicated for the complete or partial reversal of the sedative effects of benzodiazepines and may be used in situations when an overdose with a benzodiazepine is known or suspected. Prior to the administration of flumazenil, necessary measures should be instituted to secure airway, ventilation and intravenous access. Flumazenil is intended as an adjunct to, not as a substitute for, proper management of benzodiazepine overdose. Patients treated with flumazenil should be monitored for resedation, respiratory depression and other residual benzodiazepine effects for an appropriate period after treatment. The prescriber should be aware of a risk of seizure in association with flumazenil treatment, particularly in long-term benzodiazepine users and in cyclic antidepressant overdose. The complete flumazenil package insert, including CONTRAINDICATIONS, WARNINGS AND PRECAUTIONS, should be consulted prior to use.

Flumazenil is not indicated in patients with epilepsy who have been treated with benzodiazepines. Antagonism of the benzodiazepine effect in such patients may provoke seizures.

Serious sequelae are rare unless other drugs or alcohol have been taken concomitantly.


Tablets should be kept at room temperature, between 15 C and 30 C (59 F and 86 F).

Side effects

The most common side effects associated with Adnil 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.


For children, the long-term effects on physical and mental/behavioral development are uncertain and may not be seen until after many years. Therefore, discuss the risks and benefits of treatment with Adnil with your doctor.

Older adults may be more sensitive to the effects of this drug, especially drowsiness and confusion. These side effects can increase the risk of falling.

During pregnancy, this medication should be used only when clearly needed. It may harm an unborn baby. However, since untreated seizures are a serious condition that can harm both a pregnant woman and her unborn baby, do not stop taking this medication unless directed by your doctor. If you are planning pregnancy, become pregnant, or think you may be pregnant, immediately talk to your doctor about the benefits and risks of using this medication during pregnancy.

This drug passes into breast milk and may have undesirable effects on a nursing infant. Consult your doctor before breast-feeding.

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These patients of each group were divided into two subgroups according to their age either 40 years and under or over. These conclusions are therefore based on speculations about social psychological processes that have been supported by previous research and theory. The immune system was stimulated to kill the bacteria, even including the persistent latent bacteria that are otherwise refractory to the immune system and antibacterial chemotherapeutic drugs alike. The neurophysiologist informed the surgeon that evoked potential change in latency or amplitude met warning criteria. Proper interpretation and analysis of censored events and studies that contain them. Pharmacotherapy is also often helpful with stimulants considered the drugs of choice. The proteins produced from these expression systems were purified to allow testing for protective efficacy in an H. To assess the relationships between cytoskeletal changes and apical-basal polarity during healing of mechanical scrape injuries in the cat corneal endothelium.

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Effect of neonatal gonadectomy on the postnatal development of LHRH cell subtypes in male and female rats. Effects of chronic DDT intoxication in rats on lipids and other constituents of liver. Individualized HRQL was evaluated at 6 and 24 weeks post-stroke using the Patient Generated Index (PGI). No beneficial effect of intrathecal methylprednisolone acetate in postherpetic neuralgia patients. APS could alleviate insulin resistance and ER stress induced by high glucose in vivo and in vitro, respectively. Presynaptic inhibition preferentially reduces in NMDA receptor-mediated component of transmission in rat midbrain dopamine neurons. These findings may suggest that specificity of host-parasite interactions are mediated by genetic and especially epistatic components whereas maternal effects constitute a more general form of resistance. Because the plasma corticosterone level increases concomitantly with these metabolic and behavioral changes, the involvement of corticosterone has been hypothesized.

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Accordingly, the high-frequency discharges of these neurons may serve to create, under multiple extrahippocampal control and within limited periods, stable engrams for specific spatial sites in the association cortex where the cognitive map probably resides. Colloidal aluminum hydroxide gel and magnesium hydroxide in the management of peptic ulcers. There is no short supply of known ICU causing allergens, but it is equally important to be ever vigilant in precose medication recognizing, and even adding to, items in the constantly expanding list of novel allergenic agents provided to us by the advances of modern chemistry and technology, and by the changing social structure and lifestyle dynamics. Analysis of sporadic tumors derived from the revertant cells reveals an increased dosage of the transforming allele. We recommend early surgical intervention before the onset of gastrointestinal complications if ingested multiple magnets have not moved on the follow-up radiograph. Frameshift mutation (p.Leu317PhefsX12) in POU3F4 leads to the truncation of the C-terminal 44 amino acids spanning the POU domain and NLS. Isomyosin expression patterns in embryonic chicken atria during the first two weeks of development were analyzed immunohistochemically. The aims of this study were to investigate the impact of weather and hydrological conditions on Escherichia coli (E. A study was undertaken to investigate the role of MMP-12 in the development of COPD in human smokers.

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