Paxil

[Paroxetine]

Side Effects & Drug Interactions
ADVERSE REACTIONS

Adverse Reactions Associated With Discontinuation of Treatment:

Twenty percent (1,199/ 6,145) of patients treated with PAXIL in worldwide clinical trials in major depressive disorder and 16.1% (84/ 522), 11.8% (64/ 542), 9.4% (44/ 469), 10.7% (79/ 735), and 11.7% (79/ 676) of patients treated with PAXIL in worldwide trials in social anxiety disorder, OCD, panic disorder, GAD, and PTSD, respectively, discontinued treatment due to an adverse event. The most common events ( 1%) associated with discontinuation and considered to be drug related (i. e., those events associated with dropout at a rate approximately twice or greater for PAXIL compared to placebo) included the following:

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Commonly Observed Adverse Events

Major Depressive Disorder

The most commonly observed adverse events associated with the use of paroxetine (incidence of 5% or greater and incidence for PAXIL at least twice that for placebo, derived from Table 1) were: Asthenia, sweating, nausea, decreased appetite, somnolence, dizziness, insomnia, tremor, nervousness, ejaculatory disturbance, and other male genital disorders.

Obsessive Compulsive Disorder

The most commonly observed adverse events associated with the use of paroxetine (incidence of 5% or greater and incidence for PAXIL at least twice that of placebo, derived from Table 2) were: Nausea, dry mouth, decreased appetite, constipation, dizziness, somnolence, tremor, sweating, impotence, and abnormal ejaculation.

Panic Disorder

The most commonly observed adverse events associated with the use of paroxetine (incidence of 5% or greater and incidence for PAXIL at least twice that for placebo, derived from Table 2) were: Asthenia, sweating, decreased appetite, libido decreased, tremor, abnormal ejaculation, female genital disorders, and impotence.

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