starting PRISTIQ. Caution should be exercised in treating patients with
pre-existing hypertension or other underlying conditions that might be
compromised by increases in blood pressure. Cases of elevated blood
pressure requiring immediate treatment have been reported. For patients
who experience a sustained increase in blood pressure, either dose
reduction or discontinuation should be considered.
* SSRIs and SNRIs, including PRISTIQ, may increase the risk of bleeding
events. Concomitant use of aspirin, NSAIDs, warfarin, and other
anticoagulants may add to this risk.
* Mydriasis has been reported in association with PRISTIQ; therefore,
patients with raised intraocular pressure or those at risk of acute
narrow-angle glaucoma (angle-closure glaucoma) should be monitored.
* PRISTIQ is not approved for use in bipolar depression. Prior to
initiating treatment with an antidepressant, patients should be
adequately screened to determine the risk of bipolar disorder.
* As with all antidepressants, PRISTIQ should be used cautiously in
patients with a history or family history of mania or hypomania, or with
a history of seizure disorder.
* Caution is advised in administering PRISTIQ to patients with
cardiovascular, cerebrovascular, or lipid metabolism disorders.
Increases in blood pressure and small increases in heart rate were
observed in clinical studies with PRISTIQ. PRISTIQ has not been
evaluated systematically in patients with a recent history of myocardial
infarction, unstable heart disease, uncontrolled hypertension, or
cerebrovascular disease.
* Dose-related elevations in fasting serum total cholesterol, LDL (low
density lipoprotein) cholesterol, and triglycerides were observed in
clinical stud
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