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Region: CA
City: San Francisco
Postal Code: 94107
Latitude: 37.76969909668
Longitude: -122.39330291748
Area Code: 415
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KEVEYIS® (dichlorphenamide) | Primary Periodic Paralysis

KEVEYIS can help you gain greater control over the disease by decreasing the number, severity, and duration of attacks. 1,2 KEVEYIS is the only FDA-approved treatment for Primary Periodic Paralysis (PPP), a condition that can cause prolonged attacks of muscle weakness and even temporary paralysis. 1-3 Learn more about KEVEYIS

KEVEYIS® (dichlorphenamide): Treatment for Primary

Please visit to view our Important Safety Information and Full Prescribing Information KEVEYIS, granted orphan drug designation in the United States, is the first and only FDA-approved treatment for hyperkalemic, hypokalemic, and related variants of Primary Periodic Paralysis — an ultra-rare neuromuscular disorder.1 KEVEYIS Has Been Proven to Reduce Attacks in 2 Clinical

Strongbridge Biopharma plc Presents KEVEYIS

For additional KEVEYIS important safety information and the full prescribing information visit Contacts: Corporate and Media Relations Elixir Health Public Relations Lindsay Rocco +1 862-596-1304 [email protected] Investor Relations U.S.: Solebury Trout Marcy Nanus +1 646-378-2927 [email protected] Europe: First House Geir Arne

Strongbridge Biopharma plc Presents KEVEYIS

Strongbridge Biopharma plc Presents KEVEYIS® (dichlorphenamide) Primary Periodic Paralysis (PPP) Data at the 2019 American Academy of Neurology Annual Meeting

Strongbridge Biopharma plc Presents KEVEYIS

~ Results Demonstrate Long-term Treatment with KEVEYIS is Efficacious and Provides Durable Reduction in Attack Frequency and Severity in Patients with PPP ~ DUBLIN, Ireland and. - WHOIS & Domain Info - DomainBigData is hosted in Lansing, Michigan, United States and is owned by Taro Domain Manager (Taro Pharmaceuticals U.s.a. Inc). was created on 2015-07-28. Website IP is

Taro to Make Keveyis™ Available to Distributors Free of

For additional safety information, please see Full Prescribing Information at The release will be accessible on Taro’s website at About Taro™-Distributors-Free-Cost

FDA Approves Drug for Primary Hyperkalemic and Hypokalemic

Statement from MDA Executive Vice President and Chief Medical and Scientific Officer Valerie A. Cwik, M.D.: “We couldn’t be more pleased for our families affected by hyperkalemic and hypokalemic periodic paralysis, as the first treatment for these diseases has been approved by the U.S. Food and Drug Administration (FDA) and is expected to be available in the coming months.”

FDA Approves Taro’s Keveyis™ (dichlorphenamide) 50 mg

HAWTHORNE, N.Y.--(BUSINESS WIRE)--Taro Pharmaceutical Industries Ltd. (NYSE:TARO) announced today that the U.S. Food and Drug Administration (FDA) has approved Keveyis™ (dichlorphenamide) 50 mg’s-Keveyis™-dichlorphenamide-50-mg

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