An Wei De

Uses

An Wei De is used for the short-term treatment of insomnia. An Wei De has been shown to decrease the time to sleep onset for up to 30 days in controlled clinical trials.

An Wei De is also used to associated treatment for these conditions: Insomnia

How An Wei De works

An Wei De exerts its action through subunit modulation of the GABA_BZ receptor chloride channel macromolecular complex. An Wei De also binds selectively to the brain omega-1 receptor located on the alpha subunit of the GABA-A/chloride ion channel receptor complex and potentiates t-butyl-bicyclophosphorothionate (TBPS) binding.

Dosage

An Wei De dosage

The dose of An Wei De should be individualized. The recommended dose of An Wei De for most non elderly adults is 10 mg. For certain low weight individuals, 5 mg may be a sufficient dose. Although the risk of certain adverse events associated with the use of An Wei De appears to be dose dependent, the 20 mg dose has been shown to be adequately tolerated and may be considered for occasional patient who does not benefit from a trial of lower dose. Dosage above 20 mg has not been adequately evaluated and is not recommended.An Wei De should be taken immediately before bedtime. Taking An Wei De with or immediately after a heavy, high fat meal results in slower absorption and would be expected to reduce the effect of An Wei De on sleep latency. Elderly patients and debilitated patients appear to be more sensitive to the effects of hypnotic, and respond to 5 mg of An Wei De. The recommended dose for these patients is therefore 5 mg, doses over 10 mg are not recommended. For patients with mild to moderate renal impairment no dose adjustment is necessary.An initial dose of 5 mg should be given to patients concomitantly taking Cimetidine because ZalAn Wei De clearance is reduced in this population.

Side Effects

Side effects of An Wei De appear to be dose related. So, it is important to use the lowest possible effective dose, specially in the elderly. The side effects are usually mild and transient, the most common are diarrhoea, nausea, vomiting, vertigo, headache, asthenia, nightmare etc.

Toxicity

Side effects include abdominal pain, amnesia, dizziness, drowsiness, eye pain, headache, memory loss, menstrual pain, nausea, sleepiness, tingling, weakness

Precaution

Timing of drug administration: An Wei De should be taken immediately before bedtime or after the patient has gone to bed.Use in the elderly and/or debilitated patients: Impaired motor and/or cognitive performance after repeated exposure or unusual sensitivity to sedative/hypnotic drugs is a concern in the treatment of elderly and/or debilitated patients. A dose of 5 mg is recommended for elderly patients to decrease the possibility of side effects. Elderly and/or debilitated patients should be monitored closely.Use in patients with concomitant illness: An Wei De should be used with caution in patients with diseases or conditions that could affect metabolism or haemodynamic responses. Although preliminary studies did not reveal respiratory depressant effects at hypnotic doses of An Wei De in normal subjects, caution should be observed if An Wei De is prescribed to patients with compromised respiratory function, because sedative/hypnotic have the capacity to depress respiratory drive. However, patients with compromised respiration due to preexisting illness should be monitored carefully. The dose of An Wei De should be reduced to 5 mg in patients with mild to moderate hepatic impairment. It is not recommended for use in patients with severe hepatic impairment.Renal impairment patients: No dose adjustment is necessary in patients with mild to moderate renal impairment. An Wei De has not been adequately studied in patients with severe renal impairment.Use in patients with depression: As with other sedative or hypnotic drugs, An Wei De should be administered with caution to patients exhibiting signs or symptoms of depression

Interaction

An Wei De has been shown to have minimal effects on the kinetic of Warfarin, Imipramine, Ethanol, Ibuprofen, Diphenhydramine, Thioridazine, and Digoxin.

Food Interaction

• Avoid alcohol. Ingesting alcohol may increase the CNS depressant effects of zaleplon.
• Do not take with or immediately after a high-fat meal. The effects of zaleplon are reduced when taken with a high-fat meal.

[Moderate] GENERALLY AVOID: Alcohol may potentiate some of the pharmacologic effects of zaleplon.

Use in combination may result in additive central nervous system depression and
ADJUST DOSING INTERVAL: Administration of zaleplon with a high-fat or heavy meal may delay the onset of hypnotic effects.

In healthy adult subjects, administration of zaleplon with a high-fat meal resulted in a 2-hour delay in the time to reach peak plasma drug concentration (Tmax) and a 35% reduction in the peak plasma drug concentration (Cmax) compared to fasting.

An Wei De systemic exposure (AUC) and elimination half-life were not significantly affected.

MANAGEMENT: Patients receiving zaleplon should be advised to avoid the consumption of alcohol.

For faster sleep onset, zaleplon should not be administered with or immediately after a high-fat or heavy meal.

An Wei De Drug Interaction

Moderate: aripiprazole, duloxetine, escitalopram, eszopiclone, pregabalin, alprazolam, cetirizineUnknown: amphetamine / dextroamphetamine, zolpidem, ubiquinone, omega-3 polyunsaturated fatty acids, metoprolol, esomeprazole, albuterol, montelukast, cyanocobalamin, ascorbic acid, ergocalciferol, cholecalciferol, lisdexamfetamine

An Wei De Disease Interaction

Major: alcohol intox, depression, drug dependence, liver diseaseModerate: glaucoma, liver disease, resp depression, renal dysfunction

Volume of Distribution

• 1.4 L/kg

Elimination Route

Absorption An Wei De is rapidly and almost completely absorbed following oral administration.

Half Life

Approximately 1 hour

Clearance

• 1 L/h/kg

Elimination Route

An Wei De is metabolized primarily by the liver and undergoes significant presystemic metabolism. After oral administration, zaleplon is extensively metabolized, with less than 1% of the dose excreted unchanged in urine. Renal excretion of unchanged zaleplon accounts for less than 1% of the administered dose.

Pregnancy & Breastfeeding use

Pregnancy: There are no studies of An Wei De in pregnant women; therefore, it is not recommended for use in women during pregnancy. An Wei De has no established use in labour and delivery.Lactation: A study in lactating mothers indicated that the clearance and half-life of An Wei De is similar to that in young normal subjects. A small amount of An Wei De is excreted in breast milk, with the highest excreted amount occurring during a feeding at approximately 1 hour after An Wei De administration. Since the small amount of the drug from breast milk may result in potentially important concentrations in infants, and because the effects of An Wei De on a nursing infant are not known, it is not recommended in nursing mothers.

Contraindication

An Wei De is contraindicated in patients with known hypersensitivity to any of its components.

Special Warning

Special Patient Group: Patients on cimetidine should receive initial dose of 5 mg at bedtime.Hepatic Impairment:

• Mild to moderate: 5 mg at bedtime.
• Severe: Contraindicated.

Paediatric use

: The safety and effectiveness of An Wei De in paediatric patients have not been established.

Innovators Monograph

You find simplified version here An Wei De