Clinical trials have shown a response rate of over 60% and a 52% remission rate in patients treated with SPRAVATO® with minimal side effects.
SPRAVATO (generic name: esketamine) is a prescription nasal spray primarily used to treat adults with treatment-resistant depression (TRD) and major depressive disorder (MDD) accompanied by acute suicidal ideation or behavior. It is administered in the doctor’s office, where patients are monitored for 2 hours.
Unlike traditional antidepressants that target serotonin or norepinephrine, SPRAVATO works by blocking the NMDA receptor, which affects glutamate, a neurotransmitter involved in mood regulation. This mechanism can help rapidly improve symptoms of depression, often within hours to days, unlike traditional antidepressants, which can take weeks.
SPRAVATO is for use alone or in combination with an oral antidepressant for Adults with treatment-resistant depression (MDD patients who have had an inadequate response to 2 or more oral antidepressants).
SPRAVATO is for use in combination with an oral antidepressant for Depressive symptoms in adults with MDD with acute suicidal ideation or behavior (MDSI).
Your individual insurance plan determines coverage for SPRAVATO. Many major insurance companies cover it, but specific requirements like prior authorization and proof of treatment history may apply.
If you have a commercial insurance plan, there is a copay assistance program that may reduce the cost of the medication to as little as $10 per treatment.
At this time, Nashville Neurocare can see patients with the following insurance providers:
If you have questions about your coverage or eligibility, feel free to contact us—we’re happy to help verify your benefits and guide you through the process. Coverage for SPRAVATO can vary depending on your insurance plan.
Start with 56 mg or 84 mg, alone or in combination with an oral antidepressant, and an individualized dosing schedule. Evidence of therapeutic benefit should be evaluated at the end of the induction phase to determine need for continued treatment.
Start with 56 mg or 84 mg
Evidence of therapeutic benefit should be evaluated at the end of the induction phase to determine need for continued treatment.
*SPRAVATO® [Prescribing Information]. Titusville, NJ: Janssen Pharmaceuticals, Inc.
Stay well hydrated the day before your treatment. It helps with any nausea that may be experienced. Do not have anything to eat two hours before your appointment and nothing to drink an hour before. Take all your current medications as prescribed – unless directed otherwise by the provider. Arrange a ride from the office as you are not permitted to drive yourself after treatment.
Everyone’s experience is a little different, but here are some common sensations people report during or after their first SPRAVATO session:
During the Treatment (First 40 Minutes or So):
After the Treatment:
SPRAVATO is contraindicated in patients with the following conditions:
Copyright © 2025 | All Rights Reserved