Upsher-Smith Laboratories Adds Zembrace® SymTouch® (sumatriptan) Injection To Its Access Pathways® Platinum Pass® Savings Program
Program Provides Access and Affordability for Patients Seeking Treatment for Acute Migraine
Program Provides Access and Affordability for Patients Seeking Treatment for Acute Migraine
MAPLE GROVE, Minn., Nov. 18, 2019 /PRNewswire/ -- Upsher-Smith Laboratories, LLC (Upsher-Smith) today announced that it has added Zembrace® SymTouch® (sumatriptan) Injection 3 mg to its Access Pathways® Platinum Pass® Program – a savings and support program where eligible patients pay $0 per prescription. Zembrace SymTouch is indicated for the acute treatment of migraine with or without aura in adults.1 It provides migraine pain relief in as little as 10 minutes for some patients.1 Zembrace SymTouch joins Qudexy® XR (topiramate) Extended-Release Capsules and Tosymra™ (sumatriptan) Nasal Spray as part of Upsher-Smith's portfolio of medications supported by the program.
The Access Pathways Program is a best-in-class co-pay program designed to reduce out-of-pocket costs for patients and improve prescribing confidence for healthcare professionals. The benefits of the Platinum Pass savings card for Zembrace SymTouch include:
"Minutes matter to migraine patients who are seeking fast pain relief," said Rusty Field, President and CEO, Upsher-Smith. "By adding fast-acting Zembrace SymTouch to the Access Pathways Program, we are able to assist patients by reducing some of the barriers associated with access and affordability, along with challenges that healthcare professionals face when prescribing."
About Zembrace SymTouch
Zembrace SymTouch is a fast-acting acute migraine treatment option that offers a simple, two-step injection process. Zembrace SymTouch contains sumatriptan 3 mg which has been shown to provide patients with migraine pain relief in as little as 10 minutes after administration (17% of patients vs. 5% for placebo), and more than half of the patients experienced migraine pain relief two hours after administration (60% of patients vs. 21% for placebo).1
More than 36 million patients suffer from migraines and surveys have shown that a majority are willing to try other acute treatment options.2,3 Patients currently using oral acute migraine options may face challenges including nausea and gastroparesis or vomiting which may delay or limit oral medication absorption.
Important Patient Safety Information for Zembrace® SymTouch®
What important information should I know about ZEMBRACE SymTouch? ZEMBRACE SymTouch can cause serious side effects, including: heart attack and other heart problems, which may lead to death. Stop using ZEMBRACE SymTouch and get emergency medical help right away if you have any of the following symptoms of a heart attack:
ZEMBRACE SymTouch is not for people with risk factors for heart disease (high blood pressure, high cholesterol levels, smoking, overweight, diabetes, family history of heart disease) unless a heart exam is done and shows no problem.
Who should not use ZEMBRACE SymTouch?
Do not use ZEMBRACE SymTouch if you have:
What should I tell my healthcare provider before taking ZEMBRACE SymTouch?
Tell your healthcare provider about all of your medical conditions and about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements.
What should I avoid while using ZEMBRACE SymTouch?
ZEMBRACE SymTouch can cause dizziness, weakness, or drowsiness. If you have these symptoms, do not drive a car, use machinery, or do anything where you need to be alert.
What are possible side effects of ZEMBRACE SymTouch?
ZEMBRACE SymTouch may cause serious side effects including:
The most common side effects of ZEMBRACE SymTouch include pain and redness at your injection site; tingling or numbness in your fingers or toes; dizziness; warm, hot, burning feeling to your face (flushing); discomfort or stiffness in your neck; feeling weak, drowsy, or tired.
This is the most important information to know about ZEMBRACE SymTouch but is not comprehensive. For more information, talk to your healthcare provider and read the Patient Information and Instructions for Use for ZEMBRACE SymTouch. You can also visit www.upsher-smith.com or call 1-888-650-3789.
You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch, or call 1-800-FDA-1088.
INDICATION AND USAGE
What is ZEMBRACE SymTouch used for?
ZEMBRACE SymTouch is a prescription medicine used to treat acute migraine headaches with or without aura in adults who have been diagnosed with migraine.
ZEMBRACE SymTouch is not used to prevent or decrease the number of migraines you have. It is not known if ZEMBRACE SymTouch is safe and effective in children under 18 years of age.
Please see Patient Information, Instructions For Use and Full Prescribing Information for ZEMBRACE SymTouch or visit www.zembrace.com.
About Upsher-Smith
Upsher-Smith Laboratories, LLC is a trusted U.S. pharmaceutical company that strives to improve the health and lives of patients through an unwavering commitment to high-quality products and sustainable growth. Since 1919, it has brought generics and brands to a wide array of customers backed by an attentive level of service, strong industry relationships, and dedication to uninterrupted supply.
As Upsher-Smith celebrates its 100-year anniversary, the company enters a new ambitious era that has been accelerated by its 2017 acquisition by Sawai Pharmaceutical Co., Ltd. Upsher-Smith and Sawai plan to leverage each other for growth worldwide and embark on an exciting new chapter as they seek to deliver the best value for their stakeholders, and most importantly, Do More Good™ for the patients they serve. For more information, visit www.upsher-smith.com.
Qudexy, Zembrace, SymTouch, Tosymra, Access Pathways, Platinum Pass and Do More Good are trademarks of Upsher-Smith Laboratories, LLC.
*Restrictions apply. Maximum of eight single-dose injections per month. Medicare, Medicaid, and other federal and state health care program patients are not eligible.
References
SOURCE Upsher-Smith Laboratories, LLC
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