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Monoamine oxidase inhibitors buspirone

Buspirone generally is well tolerated and does not cause sedation. Most common side effects include dizziness, nausea, and headaches. Drugs that inhibit CYP3A4 (e.g., verapamil, diltiazem, itraconazole, fluvoxamine, nefa-zodone, and erythromycin) can increase buspirone levels. Likewise, enzyme inducers such as rifampin can reduce buspirone levels significantly. Bupirone may increase blood pressure when coadministered with an monoamine oxidase inhibitor (MAOI). [Pg.613]

Buspirone may increase haloperidol levels and elevate blood pressure in patients taking a monoamine oxidase inhibitor (MAOI). [Pg.759]

Like the benzodiazepines, buspirone appears to be safe even when given in very high doses. The most common side effects are dizziness, light-headedness, and headache. Abuse, dependence, and withdrawal have not been reported, and buspirone administration does not produce any cross-tolerance to the benzodiazepines. Buspirone has been reported to increase blood pressure in patients taking monoamine oxidase inhibitors, and it may increase plasma levels of haloperidol if coadministered with that agent. [Pg.356]


See other pages where Monoamine oxidase inhibitors buspirone is mentioned: [Pg.228]    [Pg.372]    [Pg.1024]    [Pg.274]    [Pg.575]    [Pg.226]    [Pg.341]   
See also in sourсe #XX -- [ Pg.83 , Pg.435 ]

See also in sourсe #XX -- [ Pg.1133 ]




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