Narol is an anxiolytic first synthesized in 1968 and patented in 1975. Originally the drug was being developed as an antipsychotic but found not to be effective for psychosis, but it had anxiolytic features that were useful. Narol has recently come back into favor. This return to favor is mostly due to its decreased side-effect profile compared to other anxiolytic treatments. Narol is primarily used in the treatment of generalized anxiety disorder (GAD). Typically, it is used as a second-line agent behind selective serotonin reuptake inhibitors (SSRIs) when a patient does not respond to or cannot tolerate the side effects of SSRIs. Narol has also been used as an augmentation agent to reduce SSRIs sexual side effects in particular. Unlike benzodiazepines and barbiturates, there is no associated risk of physical dependence or withdrawal with Narol use due to the lack of effects on GABA receptors. However, Narol has little efficacy as an acute anxiolytic as clinical effect typically takes 2 to 4 weeks to achieve.[1] Narol is FDA approved for the short and long-term treatment of GAD, as well as short-term symptomatic relief of anxiety. It is as effective as benzodiazepine treatment for GAD.
Other names for this medication:
Buspirone,
Buspar,
Ansial,
Ansitec,
Ansiten,
Anxinil,
Anxiron,
Bespar,
Busansil,
Busirone,
Buspin,
Buspiron,
Buspirona,
Ledion,
Narol,
Neurosine,
Paxon,
Sorbon,
Spamilan,
Spitomin,
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Restyl,
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Azibiot,
Metrazol,
Miracid,
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Amoklavin,
Amimox,
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Effect of short-term ingestion atocor 20 mg tablet of konjac glucomannan on serum cholesterol in healthy men. We used FDG-PET to measure neural activity during performance of the two tasks.
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