NeuroStar® TMS Therapy
FDA-cleared, non-medication depression treatment
(855) 940-4867
Medically reviewed on by
Regional Medical Director Greater St. Louis
SPRAVATO® is self-administered at REMS-certified SPRAVATO® treatment centers under the supervision of a health care provider. REMS stands for Risk Evaluation and Mitigation Strategy.
SPRAVATO® is a brand name for
esketamine nasal spray, a Schedule III controlled substance derived from ketamine. This medication can cause brief sedation and dissociation in people who take it, and it has the potential to be abused. That’s why the esketamine nasal spray is only distributed to providers under the REMS program.
To understand REMS, it’s helpful to know how these providers and health care clinics become certified treatment centers. For either an outpatient or inpatient clinic to gain the status of a REMS-certified treatment center, they must go through many steps before they can begin treating patients with nasal esketamine for depression.
If you’re a patient at a certified inpatient health care setting, you won’t need to enroll in the SPRAVATO® REMS program when your provider prescribes SPRAVATO®. However, if you’re going to an outpatient center, like Greenbrook, you’ll need to enroll.
At this point, you might be wondering ‘is Spravato covered by insurance?’ The answer is “probably yes.” At Greenbrook, our care team can help you figure out the insurance side of things. The easiest way to bring nasal esketamine up with your primary care provider is to ask if they believe you’re a candidate for it.
While you can seek out nasal esketamine without a referral, any doctor, therapist, psychologist, or social worker can refer you to a certified nasal esketamine treatment center. The medication is FDA-approved for treatment-resistant depression (TRD) and major depressive disorder with suicidal ideation or behavior (MDSI).
After you’ve talked through your medical history with your PCP and any other health care providers you want to loop in, schedule an nasal esketamine spray consultation with a certified provider. Your treatment provider will conduct an assessment of your symptoms and study your medical history before giving their approval for nasal esketamine treatment. The next step is to enroll you in the REMS program. Your treatment provider will make sure you understand the risks and benefits of treating depression with nasal esketamine spray. They’ll also make sure you agree to these requirements.
Each time you receive treatment, you’ll need to:-Administer the nasal spray yourself—at Greenbrook, we give you the opportunity to practice with trainer sprayers that look and act just like the real thing but do not dispense medication
-Stay at the healthcare setting for at least two hours after treatment, after which your provider will tell you if you’re cleared to go home
-Arrange a ride home, as you will not be able to drive or operate heavy machinery until the following day after treatment
You and your provider will fill out the form and sign it. Your provider will then send the form to SPRAVATO® REMS. Once you’re enrolled, you and your provider can figure out the best treatment plan to fit your needs. A typical round of nasal esketamine spray treatment consists of 24-26 sessions in four phases.
At Greenbrook, our Care Team will communicate with your other providers — with your permission — to ensure that they stay up-to-date on your treatment and your progress. If you're struggling with treatment resistant depression and nasal esketamine spray isn’t an option, Greenbrook also provides transcranial magnetic stimulation. Learn more about how TMS works.
Take our short quiz to see if TMS therapy or nasal esketamine could be right for you
Subscribe for mental health, self-care, and TMS therapy and nasal esketamine updates for those affected by treatment-resistant depression or OCD.
Thank you for subscribing to our email list!
Oops, there was an error adding your subscription.
Please try again later.
By providing your email address, you are consenting to receive blog updates from Greenbrook TMS Inc. You may unsubscribe from these alerts at any time by following the “unsubscribe” link at the bottom of email alerts. At Greenbrook TMS Inc. we take the privacy and security of your personal information seriously. To learn more about how we protect your personal information, please refer to our Privacy Policy.
Greenbrook supports an accessible internet. If you have any questions about our accessibility features, please contact us at
(855) 940-4867 or info@greenbrooktms.com.
NeuroStar Adult Indications for Use
The NeuroStar Advanced Therapy System is indicated for the treatment of depressive episodes and for decreasing anxiety symptoms for those who may exhibit comorbid anxiety symptoms in adult patients suffering from Major Depressive Disorder (MDD) and who failed to achieve satisfactory improvement from previous antidepressant medication treatment in the current episode.
The NeuroStar Advanced Therapy System is intended to be used as an adjunct for the treatment of adult patients suffering from Obsessive-Compulsive Disorder (OCD).
NeuroStar Adolescent Indications for Use
NeuroStar Advanced Therapy is indicated as an adjunct for the treatment of Major Depressive Disorder (MDD) in adolescent patients (15-21).
Important Safety Information
NeuroStar Advanced Therapy is only available by prescription. A doctor can help decide if NeuroStar Advanced Therapy is right for you. Patients’ results may vary.
The most common side effect is pain or discomfort at or near the treatment site. These events are transient; they occur during the TMS treatment course and do not occur for most patients after the first week of treatment. There is a rare risk of seizure associated with the use of TMS therapy (<0.1% per patient).
Visit neurostar.com for full safety and prescribing information.
Important Safety Information
What is the most important information I should know about SPRAVATO®?
SPRAVATO® can cause serious side effects, including:
Do not take SPRAVATO® if you:
If you are not sure if you have any of the above conditions, talk to your healthcare provider before taking SPRAVATO®.
Before you take SPRAVATO®, tell your healthcare provider about all of your medical conditions, including if you:
Tell your healthcare provider about all the medicines that you take, including prescription and over-the-counter medicines, vitamins and herbal supplements. Taking SPRAVATO® with certain medicine may cause side effects.
Especially tell your healthcare provider if you take central nervous system (CNS) depressants, psychostimulants, or monoamine oxidase inhibitors (MAOIs) medicine. Keep a list of them to show to your healthcare provider and pharmacist when you get a new medicine.
How will I take SPRAVATO®?
What should I avoid while taking SPRAVATO®?
Do not drive, operate machinery, or do anything where you need to be completely alert after taking SPRAVATO®. Do not take part in these activities until the next day following a restful sleep. See “What is the most important information I should know about SPRAVATO®?”
What are the possible side effects of SPRAVATO®?
SPRAVATO® may cause serious side effects including:
See “What is the most important information I should know about SPRAVATO®?”
Increased blood pressure. SPRAVATO® can cause a temporary increase in your blood pressure that may last for about 4 hours after taking a dose. Your healthcare provider will check your blood pressure before taking SPRAVATO® and for at least 2 hours after you take SPRAVATO®. Tell your healthcare provider right away if you get chest pain, shortness of breath, sudden severe headache, change in vision, or seizures after taking SPRAVATO®.
Problems with thinking clearly. Tell your healthcare provider if you have problems thinking or remembering.
Bladder problems. Tell your healthcare provider if you develop trouble urinating, such as a frequent or urgent need to urinate, pain when urinating, or urinating frequently at night.
The most common side effects of SPRAVATO® include:
If these common side effects occur, they usually happen right after taking SPRAVATO® and go away the same day.
These are not all the possible side effects of SPRAVATO®.
Call your doctor for medical advice about side effects. You may report side effects to Johnson & Johnson at 1-800-526-7736, or to the FDA at 1-800-FDA-1088.
What is SPRAVATO® (esketamine) CIII nasal spray?
SPRAVATO® is a prescription medicine used:
SPRAVATO® is not for use as a medicine to prevent or relieve pain (anesthetic). It is not known if SPRAVATO® is safe or effective as an anesthetic medicine.
It is not known if SPRAVATO® is safe and effective for use in preventing suicide or in reducing suicidal thoughts or actions. SPRAVATO® is not for use in place of hospitalization if your healthcare provider determines that hospitalization is needed, even if improvement is experienced after the first dose of SPRAVATO®.
It is not known if SPRAVATO® is safe and effective in children.
Please see full Prescribing Information, including Boxed WARNINGS, and Medication Guide for SPRAVATO® and discuss any questions you may have with your healthcare provider.
All Rights Reserved | Greenbrook TMS NeuroHealth Centers.