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  2. Buspirone - Wikipedia

    en.wikipedia.org/wiki/Buspirone

    Buspirone, sold under the brand name Buspar among others, is an anxiolytic, a medication primarily used to treat anxiety disorders, particularly generalized anxiety disorder (GAD). [ 10 ] [ 11 ] It is a serotonin 5-HT 1A receptor partial agonist , increasing action at serotonin receptors in the brain. [ 3 ]

  3. Anxiolytic - Wikipedia

    en.wikipedia.org/wiki/Anxiolytic

    Benzodiazepines are effective in emergent and short-term treatment of anxiety disorders due to their fast onset but carry the risk of dependence. [4] Buspirone is indicated for GAD, which has much slower onset but with the advantage of less sedating and withdrawal effects. [5]

  4. Onset of action - Wikipedia

    en.wikipedia.org/wiki/Onset_of_action

    A few drugs such as alcohol are absorbed by the lining of the stomach, and therefore tend to take effect much more quickly than the vast majority of oral medications which are absorbed in the small intestine. Gastric emptying time can vary from 0 to 3 hours, [2] and therefore plays a major role in onset of action for orally administered drugs ...

  5. List of side effects of buspirone - Wikipedia

    en.wikipedia.org/wiki/List_of_side_effects_of...

    Nervousness; Insomnia; Sleep disorder; Disturbance in attention; Depression; Confusional state; Anger; Tachycardia (fast heart rate); Chest pain; Sinusitis (nasal ...

  6. Serotonin syndrome - Wikipedia

    en.wikipedia.org/wiki/Serotonin_syndrome

    Onset of symptoms is typically within a day of the extra serotonin. [2] Diagnosis is based on a person's symptoms and history of medication use. [2] Other conditions that can produce similar symptoms such as neuroleptic malignant syndrome, malignant hyperthermia, anticholinergic toxicity, heat stroke, and meningitis should be ruled out. [2]

  7. meta-Chlorophenylpiperazine - Wikipedia

    en.wikipedia.org/wiki/Meta-Chlorophenylpiperazine

    meta-Chlorophenylpiperazine (mCPP) is a psychoactive drug of the phenylpiperazine class. It was initially developed in the late-1970s and used in scientific research before being sold as a designer drug in the mid-2000s.

  8. Etifoxine - Wikipedia

    en.wikipedia.org/wiki/Etifoxine

    [2] [3] The time to peak levels of etifoxine is 2 to 3 hours. [5] The plasma protein binding of etifoxine is 88 to 95%. [4] It does not bind to blood cells. [2] The drug is known to cross the placental barrier. [2] Etifoxine is metabolized in the liver into several metabolites. [5] One of these metabolites, diethyletifoxine, is ...

  9. Azapirone - Wikipedia

    en.wikipedia.org/wiki/Azapirone

    Buspirone was originally classified as an azaspirodecanedione, shortened to azapirone or azaspirone due to the fact that its chemical structure contained this moiety, and other drugs with similar structures were labeled as such as well. However, despite all being called azapirones, not all of them actually contain the azapirodecanedione ...

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