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We are finalizing approval for device pass-through payment status for VasQ TM under the alternative pathway for devices that have an FDA Breakthrough Device designation and FDA marketing authorization for the indication for which the device has Breakthrough Device designation

Hypertension 61 , 513 (2013)

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Conversely, patients with minimal adverse effects and inadequate therapeutic response may undergo more rapid titration under careful medical supervision

You may experience amplified side effects (headache, restlessness, GI discomfort) without additional synaptogenic signaling