LAS VEGAS--(BUSINESS WIRE)--Feb 5, 2026--
Serenity Mental Health Centers, a leader in psychiatric care and one of the fastest growing mental health providers in the nation, is helping redefine access to Transcranial Magnetic Stimulation (TMS) therapy in Las Vegas.
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Serenity’s board-certified psychiatrists and psychiatric mental health nurse practitioners provide full-spectrum mental health services tailored to each patient’s needs. Treatments include psychiatric evaluations, medication management, TMS, and ketamine infusion therapy for conditions such as depression, anxiety, PTSD, OCD, and more. These evidence-based approaches are designed for patients seeking both traditional support and non-medication treatment options.
“When people ask where to get TMS therapy in Las Vegas, they’re often looking for a treatment they can trust,” said Tricia Pease, COO and co-founder of Serenity Mental Health Centers. “We focus on providing TMS in a supportive outpatient setting.”
Serenity’s outpatient model includes flexible scheduling and same-day appointments, breaking down barriers that often prevent patients from receiving timely care. Serenity is committed to providing patient-first psychiatry and to becoming the go-to destination for TMS therapy in Las Vegas.
With an 84% response rate and 78% remission rate for TMS patients, Serenity’s Las Vegas clinic is considered one of the best TMS therapy clinics for those seeking alternatives to medication.
To book an appointment, visit http://serenitymentalhealthcenters.com/nevada-psychitry-clinics/las-vegas/ or call 725-201-1842.
About Serenity Mental Health Centers
Serenity Mental Health Centers is a leading provider of comprehensive mental health services, dedicated to transforming the lives of patients through compassionate, innovative, and evidence-based care. With 35 locations across the country, Serenity offers a wide range of treatments tailored to address various mental health conditions, including depression, anxiety, OCD and PTSD. Our highly skilled team of psychiatrists, nurse practitioners and mental health specialists combine innovative therapies like Transcranial Magnetic Stimulation (TMS) and ketamine infusion with personalized care to help patients achieve lasting wellness. Serenity is committed to expanding access to quality mental health care and fostering hope and recovery for individuals and families in the communities we serve. For more information, go to serenitymentalhealthcenters.com.
Serenity Mental Health Centers provides psychiatric services in Las Vegas.
WILMINGTON, Del.--(BUSINESS WIRE)--Feb 5, 2026--
AOP Health US, LLC announced today that Rapiblyk® (landiolol) is now more widely available across the United States through contract with Vizient®, the nation’s largest provider-driven healthcare performance improvement company. Hospitals and health systems nationwide now have increased access through the Vizient catalog to Rapiblyk®, enhancing flexibility while expanding the availability of this critical care therapy.
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Furthermore, through the Vizient contract, participating hospital clients may have enhanced access to tiered pricing and streamlined ordering.
“This represents an important milestone in ensuring that Rapiblyk availability is secured nationwide, supporting clinicians and healthcare providers in critical care environments,” said John Kimmet,General Manager of AOP Health US. “We’re reinforcing our commitment to making Rapiblyk accessible where it’s needed most.”
AOP Health US previously announced the U.S. commercial availability of Rapiblyk® (landiolol), an ultra-short-acting, selective beta-1 adrenergic receptor blocker approved by the U.S. Food and Drug Administration (FDA) for the short-term reduction of ventricular rate in adults with supraventricular tachycardia (SVT) or irregular rapid heart rate, including atrial fibrillation and atrial flutter, in critical care settings
Prescribing information can be found at www.rapiblyk.com
About Rapiblyk®
Rapiblyk® (landiolol) is an ultra-short-acting, selective beta-1 adrenergic receptor blocker indicated for the short-term reduction of ventricular rate in adults with supraventricular tachycardia (SVT) or irregular rapid heart rate, including atrial fibrillation and atrial flutter, especially in perioperative, postoperative, or critical-care settings. Rapiblyk® provides rapid onset and offset of action, allowing clinicians to achieve precise, controlled rate management with a favorable hemodynamic profile.
The product is supplied as an intravenous infusion designed for use in a monitored hospital setting.
INDICATION
Rapiblyk® is indicated for the short-term reduction of ventricular rate in adults with supraventricular tachycardia, including atrial fibrillation and atrial flutter.
IMPORTANT SAFETY INFORMATION
CONTRAINDICATIONS
Rapiblyk® is contraindicated in patients with:
WARNINGS AND PRECAUTIONS
Includes risk of hypotension, bradycardia, cardiac failure, bronchospasm, masking of hypoglycemia symptoms, infusion site reactions, worsening of Prinzmetal’s angina, complications in pheochromocytoma, peripheral vascular disease, abrupt withdrawal effects, hyperkalemia, metabolic acidosis, and unresponsiveness to epinephrine in hypersensitivity reactions.
ADVERSE REACTIONS
Most important and common adverse reaction is hypotension which in clinical trials occurred in 9.9% of patients receiving RAPIBLYK® vs. 1% in those receiving placebo. Please consult the full Prescribing Information for Rapiblyk®: https://www.accessdata.fda.gov/drugsatfda_docs/label/2024/217202s000lbl.pdf
About AOP Health
AOP Health is a global enterprise with roots in Austria and a mission to address unmet medical needs through innovative, science-driven therapies in cardiovascular and rare disease. Since 1996, the AOP Health Group has been recognized as a pioneer in developing integrated therapy solutions that combine deep scientific expertise with a strong commitment to patient and physician needs.
Building on this foundation, AOP Health US, LLC was established in 2025 to expand the company’s impact in the United States. The team is focused on introducing its 2024 US FDA approved product for use in the critical care setting, while building the infrastructure to support healthcare professionals and the patients they serve.
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