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MAPLE GROVE, Minn., Oct. 25, 2018 /PRNewswire/ -- Upsher-Smith Laboratories, LLC (Upsher-Smith) today announced that it will be attending the American Academy of Neurology (AAN) 2018 Fall Conference in Las Vegas, October 26-28, 2018. Upsher-Smith representatives will be available at booth #415 to discuss Qudexy^® XR (topiramate) extended-release capsules and Platinum Pass™, the latest addition to the Access Pathways^® Program. Once-daily Qudexy^® XR is indicated for use in the prevention of migraine headaches in adults and adolescents 12 years of age and older and is also indicated to treat certain types of seizures in patients 2 years and older.  

Topiramate is the most commonly prescribed migraine preventive, with a sizable body of evidence that supports its use.¹ The AAN and the American Headache Society have given topiramate a "top tier" rating for migraine prevention in adults.²  For patients with frequent migraine attacks (1-2 per week or more), many doctors recommend daily preventative therapy.³

About Platinum Pass™
The Platinum Pass™ makes it easier than ever for physicians to prescribe Qudexy^® XR for migraine prevention or certain types of seizures while offering patients cost savings. The program is designed to eliminate barriers associated with prescribing and provides healthcare professionals with the tools necessary to help their patients Start, Stay and Save on Qudexy^® XR therapy.

Patients can present the Platinum Pass™ to their pharmacist for instant savings that last all year (365 days of therapy). Features include:

• $0 Per Prescription – Regardless of Coverage*
• Good for a Maximum of 365 Days of Therapy Over the Next 12 Months – Renewable Annually
• No Activation Required Prior to Going to a Preferred Pharmacy

The Access Pathways^® Program also includes prior authorization support^†, pharmacy stocking assistance, and a Qudexy^® XR "Pay No More Than" option for patients with no insurance. To learn more, please visit hcp.QudexyXR.com or call 1-855-282-4887 Monday-Friday from 8:00 a.m. – 7:00 p.m. (EST).

WHAT IS QUDEXY XR?

Qudexy^® XR (topiramate) Extended-Release Capsules is a prescription medicine used for:

• Migraine: To prevent migraine headaches in adults and adolescents 12 years and older.
• Monotherapy Epilepsy: Initial monotherapy to treat certain types of seizures (partial-onset seizures and primary generalized tonic-clonic seizures) in adults and children 2 years and older.
• Adjunctive Epilepsy: Adjunctive therapy to treat certain types of seizures (partial-onset seizures, primary generalized tonic-clonic seizures, and seizures associated with Lennox-Gastaut syndrome) in adults and children 2 years and older.

WHAT IMPORTANT SAFETY INFORMATION SHOULD I KNOW ABOUT QUDEXY XR?

Qudexy^® XR should not be taken by patients with metabolic acidosis who are also taking a medicine called metformin.

What should I tell my healthcare provider BEFORE starting Qudexy XR?

Tell your healthcare provider if you take any medicines that impair or decrease thinking, concentration, or muscle coordination; medicines used to prevent seizures; any other carbonic anhydrase inhibitors; or birth control pills. Qudexy XR may make birth control pills less effective.

Qudexy XR can cause serious side effects, including:

• Serious eye problems, including blurred or sudden decrease in vision and increased pressure in the eye, which can lead to permanent vision loss.
• Decreased sweating and fever, especially in hot weather which may result in hospitalization; children are especially susceptible to these effects.
• Increased acid level in the blood (metabolic acidosis), which may lead to brittle or soft bones (osteoporosis, osteomalacia, osteopenia), kidney stones, slowed rate of growth in children and fetal harm. Metabolic acidosis may or may not cause symptoms. Symptoms may include feeling tired, decreased appetite, change in heartbeat, or trouble thinking clearly.
• High ammonia level in the blood, which can affect mental activities, slow alertness and cause tiredness and vomiting. This can also happen when Qudexy XR is taken with a medicine called valproic acid.
• Kidney stone formation, which may be reduced by increasing fluid intake while taking Qudexy XR.
• Low body temperature. Taking Qudexy XR while taking valproic acid may cause a drop in body temperature to less than 95°F with associated symptoms of tiredness, confusion, or coma.
• Effects on thinking and alertness. Qudexy XR may affect thinking, and cause confusion and problems with concentration, attention, memory, or speech. Qudexy XR may cause depression or mood problems, tiredness, and sleepiness.
• Dizziness or loss of muscle coordination.
• Fetal harm. Taking Qudexy XR while pregnant increases the fetus risk of cleft lip and/or cleft palate and of being small for gestational age. Alternative treatment or effective birth control should be used. Discuss with your healthcare provider.
• Suicidal thoughts and actions. Like other antiepileptic drugs, Qudexy XR may cause suicidal thoughts and actions in a very small number of people, about 1 in 500. Tell your healthcare provider right away if you experience these effects, or any symptoms of depression or mood changes.

Tell your healthcare provider right away if you have any of the above symptoms, are planning to become pregnant, or if you become pregnant while taking
Qudexy XR.

The most common side effects of Qudexy XR include: tingling of the arms and legs (paresthesia), not feeling hungry, weight loss, nervousness, nausea, speech problems, tiredness, dizziness, sleepiness/drowsiness, a change in the way foods taste, upper respiratory tract infection, slow reactions, difficulty with memory, fever, abnormal vision, diarrhea, and pain in the abdomen. These are not all the possible side effects of Qudexy XR. For more information, ask your healthcare provider or pharmacist.

Before taking Qudexy XR, tell your healthcare provider about all of your medical conditions, including if you: have had depression, mood problems, or suicidal thoughts or behavior; have kidney problems, kidney stones, or are getting kidney dialysis; have a history of metabolic acidosis (too much acid in the blood); have liver problems; have weak, brittle or soft bones (osteomalacia, osteoporosis, osteopenia, or decreased bone density); have lung or breathing problems; have eye problems, especially glaucoma; have diarrhea; have a growth problem; are on a diet high in fat and low in carbohydrates, which is called a ketogenic diet; are having surgery; are pregnant or plan to become pregnant; or if you are breastfeeding. The medicine in Qudexy XR (topiramate) passes into your breast milk. It is not known if the medicine, topiramate, that passes into breast milk can harm your baby. Talk to your healthcare provider about the best way to feed your baby if you take Qudexy XR.

Qudexy XR should not be taken while drinking alcohol, as this can cause serious side effects such as severe sleepiness, dizziness, and an increase in seizures.

Patients taking Qudexy XR should not drive, swim, climb, or operate heavy machinery until it is known how Qudexy XR affects them. Qudexy XR can slow thinking and motor skills and may affect vision. Some patients with epilepsy taking Qudexy XR will continue to have unpredictable seizures.

Do not stop Qudexy XR without first talking to a healthcare provider. If you have epilepsy and you stop taking Qudexy XR suddenly, you may have seizures that do not stop.

This is the most important information to know about Qudexy XR, but is not comprehensive. For more information, talk to your healthcare provider and read the Medication Guide for Qudexy XR. You can also visit www.upsher-smith.com for the full Prescribing Information 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.

Qudexy, Access Pathways and Platinum Pass are trademarks of Upsher-Smith Laboratories, LLC.

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. As we approach our 100^th year in business, we enter a new ambitious era that has been accelerated by our 2017 acquisition by Sawai Pharmaceutical Co., Ltd. Together, we seek to deliver the best value for our stakeholders, and most importantly, do more good for the patients we serve. For more information, visit www.upsher-smith.com.

References

1. Silberstein SD. Topiramate in Migraine Prevention: A 2016 Perspective. Headache. 2017 Jan;57(1):165-178.
   
   
2. Silberstein SD, Holland S, Freitag F, Dodick DW, Argoff C, Ashman E. Evidence-based guideline update: pharmacologic treatment for episodic migraine prevention in adults: report of the Quality Standards Subcommittee of the American Academy of Neurology and the American Headache Society. Neurology. 2012;78(17):1337-1345.
   
   
3. American Headache Society. Available at https://americanheadachesociety.org/wp-content/uploads/2018/05/Alan_Rapoport_-_Migraine_Prevention_Medications.pdf. Accessed October 15, 2018.

*Restrictions apply. Medicare, Medicaid, and other state and federal health care program patients are not eligible.

†For FDA-approved indications only.

113846.01

SOURCE Upsher-Smith Laboratories, LLC