Spravato®
First FDA-approved nasal spray proven to relieve symptoms of treatment-resistant depression (TRD).
Find out if Spravato® is Right for you Call UsSpravato®
Depression is treatable, but standard therapies and medications don't help everyone. Dedicated to providing comprehensive, cutting-edge care, experienced psychiatrist Dinar Sajan, MD, and her team at Health & Psychiatry offer SPRAVATO® which is the first FDA approved nasal spray for treatment-resistant depression in adults.
If you've tried two or more antidepressants* without sufficient relief, contact one of our offices across Florida by phone, or you can request an appointment online today to see if you may have treatment-resistant depression.
What is Spravato®?
SPRAVATO®, the first FDA-approved esketamine nasal spray medication specifically developed for adults with treatment-resistant depression or the depression that has not improved after trying at least two different antidepressants.
SPRAVATO® works by targeting the N-methyl-D-aspartate (NMDA) receptor in the brain, which is part of the glutamate system. This mechanism is different from traditional antidepressants that primarily affect serotonin, norepinephrine, or dopamine. By acting on the NMDA receptor, SPRAVATO help reset brain pathways involved in mood regulation, often leading to faster symptom improvement. Spravato is the only medication on the market that works through this pathway making it a truly unique experience.
Book an Appointment Call UsWho Can Benefit from Spravato®
SPRAVATO® is prescribed alongside an oral antidepressant for adults who:
- Have treatment-resistant depression (TRD): depression that hasn't improved after trying two or more antidepressants
- OR
- Experience depressive symptoms with suicidal ideation as part of major depressive disorder (MDD)
Before You Begin
Before beginning SPRAVATO®, patients should understand:
- It is not a pain medication or anesthetic
- It does not replace hospitalization if your provider determines inpatient care is necessary
What to Expect During Your SPRAVATO® Treatment?
Spravato® is always administered under the direct supervision of a healthcare provider in a controlled clinical environment.
Click on these steps to review details.
- Your blood pressure is checked before each dose.
- If your blood pressure is elevated (for example, above 140/90 mmHg), your provider will evaluate whether treatment is safe that day.
- Spravato® will not be administered if increased blood pressure or intracranial pressure poses a significant risk.
- You will self-administer the nasal spray under provider guidance.
- Your blood pressure will be reassessed approximately 40 minutes after dosing and monitored as needed.
- You will remain in the office for at least two hours for observation, in accordance with national safety guidelines.
Patients spend this time in a quiet, low-stimulus environment. You may:
- Sit in a comfortable recliner
- Listen to music
- Watch a movie or use a device with headphones
- Rest, meditate, or simply relax
Many individuals find this time restorative and supportive to the overall treatment experience.
- Patients may drive to the appointment, but are not permitted to drive afterwards.
- A responsible adult, ride share, or arranged transportation must be used.
- Spravato® recommends avoiding driving until you have had a full night of sleep, even if you feel alert.
Side Effects and Safety
Information for SPRAVATO®
SPRAVATO® can cause serious side effects. It's important to understand what to expect and when to seek help.
Common Side Effects During Treatment
Sedation and Dissociation
Some patients experience sedation or dissociation during treatment, which may include:
- Feeling sleepy, dizzy, or faint
- Experiencing a spinning sensation
- Feeling disconnected from yourself, your thoughts, or your surroundings
If you feel unable to stay awake or feel like you might pass out, inform your healthcare provider immediately.
Important Safety Considerations
Suicidal Thoughts and Behaviors
Like other antidepressants, SPRAVATO® may increase the risk of suicidal thoughts or actions, particularly in individuals under 24 years old during the first few months of treatment or when doses are adjusted. SPRAVATO® is not approved for use in children.
Blood Pressure and Cardiovascular Considerations
SPRAVATO® may temporarily increase blood pressure, which is why careful monitoring is required before, during, and after each treatment session.
Pregnancy
SPRAVATO® is not indicated for use during pregnancy and must be stopped immediately if pregnancy occurs.
Telepsychiatry:
Expert Care From Anywhere
Access expert personality disorder therapy from the comfort and privacy of your own home through secure, HIPAA-compliant video appointments.
You can meet with one of our licensed providers, including our experienced psychiatrist, using your smartphone, tablet, or computer.
- Receive care from the comfort of your home
- Eliminate travel time and transportation barriers
- Flexible scheduling around work and family commitments
- Maintain continuity of care even when traveling
- Access to the same expert providers and personalized treatment
What to Bring
1. Driver's License
2. Insurance ID Card
3. Prescription Bottles
Your Insurance Likely Covers Your Care
We accept most major insurance plans. Let's verify your coverage before your first visit.
Frequenctly Asked Questions
Have questions about tech tools, insurance, or session flow? You’re not alone. Explore our FAQs or contact support for any help before or during your virtual visit.
Confidence and Expertise
Built on a strong foundation of accredited compliance
HIPAA Compliance
We maintain full HIPAA compliance, ensuring all healthcare data is protected with the highest level of confidentiality.
Type II SOC 2 Compliance
Being SOC 2 Type II certified highlights our commitment to rigorous security practices and safeguarding data integrity.
American Psychiatric Association
Works in coordination with the American Psychiatric Association