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Stilnox Zolpidem is used for a brief time to treat an exact sleep drawback (insomnia) in adults. If you have got hassle falling asleep, it helps you go to sleep quicker, therefore you’ll be able to get a much better night’s rest. Zolpidem belongs to a category of medication referred to as sedative-hypnotics. It acts on your brain to provide a relaxing impact.(Buy stilnox online)

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Chemistry of Stilnox

The chemical formula of Stilnox is “N,N-dimethyl-2-[6-methyl-2-(4-methylphenyl)imidazo[1,2-a]pyridin-3-yl]acetamide” as per IUPAC. Buy Stilnox 10mg Online. The molecular weight of this drug has been calculated to be 307.395 g/mol and the purity of this substance in its purest forms has been calculated to be approximately equal to or greater than 98%. The molecular formula of Stilnox is C19H21N3O. The biological half-life of the drug is 2-3 hour.

The recommended storage temperature for the drugs is either room temperature or between 20oC to 25oC while the stability of the molecule of this drug is known to be equal to or greater than two to three years.

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Usage of Stilnox

Used to initiate and maintain sleep to those with insomnia. A short-term drug should not be used for more than four weeks. It works by binding to unique sites in the brain that produce sleep. You must ask the doctor why he/she has prescribed this drug. Buy Stilnox 10mg Online

Precautions for Stilonx

You should not take Stilnox if you have a history of drug/alcohol abuse, sleep apnea, severe kidney/liver problems, myasthenia gravis, or acute lung problems.

No one below 18 years should take Stilnox. Buy Stilnox 10mg Online

Symptoms of an allergic reaction because of Stilnox include short breath, skin rash, itching, and swelling of the face, tongue, or lips, which might cause a difficulty in breathing or swallowing.

Pregnant woman or people who intend to get pregnant should not take Stilnox. The drug might affect the unborn baby if you take it during pregnancy. Consult with your doctor to learn whether the benefits of the drug outweigh the risk. Breastfeeding mothers should also avoid this medication because Stilnox can pass into breast milk and the unborn baby might be affected.

Never take this drug after the expiry date indicated on the instructions label. Doing so might be harmful. Also, do not consume the medication if its package is damaged or shows signs of tampering. Buy Stilnox 10mg Online

Let them specialist know if you have any breathing problems or you often snore while sleeping. In addition, a medical professional should know if you have a history of alcohol or any other drug or if you have suffered mental illness or depression before. If so, there is a risk that Stilnox can be habit-forming.

Tell the doctor if you are planning to get surgery or have any heart problems.

Dosage of Stilnox

Note that you should only take Stilnox when you can get a full night’s sleep. You should just take one dose in one night. The usual dose of the drug is one tablet of 10mg. Those above 65 years should divide the dose by two to 5mg. It applies to patients with a liver problem. In some cases, the doctor will determine the best treatment that is effective for you. Patients should consult with their doctor if they are unsure of the right dose for you. Do not exceed 10mg since it will impair your consciousness.

The tablet should be swallowed whole with enough water. Do not chew or crush the tablet unless the doctor tells you to divide it by half.

In case of a missed dose, just wait for the next scheduled time. Do not take the drug late in the night to make up for the lost treatment because you might have trouble waking up.

Seek medical care the moment you suspect you have overdosed.

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Special Precautions
The cause of insomnia should be identified wherever possible and the underlying factors treated before a hypnotic is prescribed. The failure of insomnia to remit after a 7-14 day course of treatment may indicate the presence of a primary psychiatric or physical disorder, and the patient should be carefully re-evaluated at regular intervals.
Psychotic Illness: Hypnotics such as zolpidem are not recommended for the primary treatment of psychotic illness.
Amnesia: Sedative/hypnotic agents such as zolpidem may induce anterograde amnesia. The condition occurs most often several hours after ingesting the product and therefore to reduce the risk patients should ensure that they will be able to have an uninterrupted sleep of 7-8 hours.
Depression: As with other sedative/hypnotic drugs, zolpidem should be administered with caution in patients exhibiting symptoms of depression. Suicidal tendencies may be present, therefore the least amount of zolpidem that is feasible should be supplied to these patients to avoid the possibility of intentional overdosage by the patient. Pre-existing depression may be unmasked during use of zolpidem. Since insomnia may be a symptom of depression, the patient should be re-evaluated if insomnia persists. General information relating to effects seen following administration of hypnotic agents which should be taken into account by the prescribing physician are described as follows.
Other Psychiatric and “Paradoxical” Reactions: Other psychiatric and paradoxical reactions like restlessness, insomnia exacerbated, agitation, irritability, aggression, delusion, anger, nightmares, hallucinations, abnormal behavior and other adverse behavioral effects are known to occur when using sedative/hypnotic agents like zolpidem. Should this occur, use of zolpidem should be discontinued. These reactions are more likely to occur in the elderly.
Somnambulism and Associated Behaviours: Sleep walking and other associated behaviours such as “sleep driving”, preparing and eating food, making phone calls or having sex, with amnesia for the event, have been reported in patients who had taken zolpidem and were not fully awake. The use of alcohol and other CNS-depressants with zolpidem appears to increase the risk of such behaviours, as does the use of zolpidem at doses exceeding the maximum recommended dose. Discontinuation of zolpidem should be strongly considered for patients who report such behaviours (for example, sleep driving), due to the risk to the patient and others (see Interactions).
Psychomotor Impairment: The risk of psychomotor impairment, including impaired driving ability, is increased if: Zolpidem is taken within less than 7-8 hours before performing activities that require mental alertness, a dose higher than the recommended dose is taken, or zolpidem is co-administered with other CNS depressants, alcohol, or with other drugs that increase the blood levels of zolpidem.
Tolerance: Some loss of efficacy to the hypnotic effects of sedative/hypnotic agents like zolpidem may develop after repeated use for a few weeks.
Dependence: Use of sedative/hypnotic agents like zolpidem may lead to the development of physical and psychological dependence. The risk of dependence increases with dose and duration of treatment; it is also greater in patients with a history of psychiatric disorders and/or alcohol or drug abuse. These patients should be under careful surveillance when receiving hypnotics.
Once physical dependence has developed, abrupt termination of treatment will be accompanied by withdrawal symptoms. These may consist of headaches or muscle pain, extreme anxiety and tension, restlessness, confusion and irritability. In severe cases the following symptoms may occur: Derealization, depersonalization, hyperacusis, numbness and tingling of the extremities, hypersensitivity to light, noise and physical contact, hallucinations or epileptic seizures.
Rebound Insomnia: A transient syndrome whereby the symptoms that led to treatment with sedative/hypnotic agents recur in an enhanced form, may occur on withdrawal of hypnotic treatment. It may be accompanied by other reactions including mood changes, anxiety and restlessness. It is important that the patient should be aware of the possibility of rebound phenomena, thereby minimizing anxiety over such symptoms should they occur when the medicinal product is discontinued.
In the case of sedative/hypnotic agents with a short duration of action, withdrawal phenomena can become manifest within the dosage interval.
Severe Injuries: Due to its pharmacological properties, zolpidem can cause drowsiness and a decreased level of consciousness, which may lead to falls and consequently to severe injuries.
Driving a Vehicle or Performing Other Hazardous Tasks: Vehicle drivers and machine operators should be warned that, as with other hypnotics, there may be a possible risk of adverse reactions including drowsiness, prolonged reaction time, dizziness, sleepiness, blurred/double vision, reduced alertness and impaired driving the morning after therapy. In order to minimise this risk a full night of sleep (7-8h) is recommended.
Furthermore, the co-administration of zolpidem with alcohol and other CNS depressants increases the risk of such effects. Patients should be warned not to use alcohol or other psychoactive substances when taking zolpidem.
Use in Children: Safety and effectiveness of zolpidem have not been established in patients below the age of 18 years. In an 8-week study in paediatric patients (aged 6-17 years) with insomnia associated with attention-deficit/hyperactivity disorder (ADHD), psychiatric and nervous system disorders comprised the most frequent treatment emergent adverse events observed with zolpidem versus placebo and included dizziness (23.5% vs. 1.5%), headache (12.5% vs. 9.2%), and hallucinations (7.4% vs. 0%) (see Special Populations under Dosage & Administration).
Use in Elderly: See Elderly under Dosage & Administration.

 

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