This article provides a comprehensive overview of biosimilar medications, highlighting their differences from biologics, approved uses for psoriasis, safety considerations, and potential side effects. It emphasizes the importance of professional supervision when using these therapies for effective and safe treatment.
Psoriasis remains a prevalent health condition in the U.S., with types such as plaque, inverse, guttate, and erythrodermic psoriasis. The disease can affect various body areas, including nails. The National Psoriasis Foundation endorses certain biosimilar therapies as part of comprehensive treatment plans.
Differences Between Biologics and Biosimilars
Biologics target specific immune system elements, reducing widespread effects. Biosimilars are highly similar to biologics but feature distinct safety and regulatory considerations.
Additionally, biosimilars generally share mechanisms of action and dosing protocols with their biologic counterparts.
Who Benefits from Biosimilars?
Biosimilars are primarily prescribed for severe psoriasis but are increasingly utilized for patients battling infections or with weakened immune systems. Safety for use in infants, pregnant women, and fetuses is still under research, reserved for critical cases.
Role of Biosimilars in Psoriasis Management
Several biosimilar drugs have gained FDA approval for psoriasis treatment, including:
Reflikimab and Inflectra, similar to Remicade
Erelzi, akin to Etanercept
Adalimumab-adbm and Adalimumab-atto, comparable to Adalimumab
Possible Side Effects
Like all medications, biosimilars may cause adverse reactions such as:
Headaches
Skin redness, warmth, swelling, soreness
Upper respiratory infections
Fever, chills
Excessive sweating
Chest and nasal congestion
Breathing difficulties
Abdominal pain
Injection site irritation
Ongoing research aims to expand biosimilars' uses beyond psoriasis. These drugs should always be used under the supervision of healthcare professionals at trusted centers like Mayo Clinic or UCSF Medical Center.