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PRODUCT INFORMATION

FIRDAPSE is the first and only FDA-approved, evidence-based therapy indicated for the treatment of Lambert-Eaton myasthenic syndrome (LEMS) in adults.1,2

INDICATION AND IMPORTANT SAFETY INFORMATION

INDICATIONS AND USAGE: 
FIRDAPSE is a potassium channel blocker indicated for the treatment of Lambert-Eaton myasthenic syndrome (LEMS) in adults.

CONTRAINDICATIONS
FIRDAPSE is contraindicated in patients with:

    • A history of seizures
    • Hypersensitivity to amifampridine phosphate or another aminopyridine


WARNINGS AND PRECAUTIONS

Seizures: FIRDAPSE can cause seizures. Consider discontinuation or dose-reduction of FIRDAPSE in patients who have a seizure while on treatment. FIRDAPSE is contraindicated in patients with a history of seizures.

Hypersensitivity: If a hypersensitivity reaction such as anaphylaxis occurs, FIRDAPSE should be discontinued and appropriate therapy initiated.


ADVERSE REACTIONS
The most common (> 10%) adverse reactions are: paresthesia, upper respiratory tract infection, abdominal pain, nausea, diarrhea, headache, elevated liver enzymes, back pain, hypertension, and muscle spasms.


Please see full Prescribing Information for additional Important Safety Information.


To report SUSPECTED ADVERSE REACTIONS, contact Catalyst Pharmaceuticals at 1-844-347-3277 (1-844-FIRDAPSE) or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.


  1. Orange Book: Approved drug products with therapeutic equivalence evaluations. US Food and Drug Administration website. https://www.accessdata.fda.gov/Scripts/cder/ob/search_product.cfm. Accessed April 24, 2019.
  2. Full Prescribing Information for FIRDAPSE (amifampridine). Catalyst Pharma.; 2018.


FIRDAPSEĀ® is a registered trademark of Catalyst Pharmaceuticals, Inc .
Ā© 2020 Catalyst Pharmaceuticals, Inc. All Rights Reserved. 20LEM0449 July 2020

LEARN MORE

Contact Information

Amanda Habel
Regional Account Manager
ahabel@catalystpharma.com
847-323-2483



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