The more commonly observed untoward events associated with the use of buspirone HCl not seen at an equivalent incidence among placebo-treated patients include:
One guide to the relative clinical importance of adverse events associated with buspirone HCl is provided by the frequency with which they caused drug discontinuation during clinical testing. Approximately 10% of the 2200 anxious patients who participated in the buspirone HCl premarketing clinical efficacy trials in anxiety disorders lasting 3 to 4 weeks discontinued treatment due to an adverse event.
The more common events causing discontinuation included:
In addition, 3.4% of patients had multiple complaints, none of which could be characterized as primary.
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