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Tag: Haegarda

Explore our medication guides and pharmacology articles within this category.

What is the brand name for C1 inhibitor concentrate?

3 min read
Over 200,000 Americans are estimated to have a rare disease known as Hereditary Angioedema (HAE), a condition caused by a deficiency or dysfunction of the C1 esterase inhibitor protein. The standard of care often involves replacing this missing protein, which is available under several different brand names for C1 inhibitor concentrate, including Berinert, Cinryze, and Haegarda.

Are HAEGARDA and Berinert the same? A Detailed Comparison for Hereditary Angioedema

4 min read
Hereditary Angioedema (HAE) is a rare genetic condition causing episodes of severe swelling due to low or malfunctioning C1 esterase inhibitor (C1-INH). While both HAEGARDA and Berinert are C1-INH replacement therapies, a crucial distinction exists regarding their use: HAEGARDA is a routine prophylactic to prevent attacks, while Berinert is an on-demand treatment for acute attacks. Understanding their separate functions is vital for managing HAE effectively.

What is the generic name for C1 esterase inhibitor?

4 min read
Hereditary angioedema (HAE) affects an estimated 1 in 50,000 people globally and is caused by a deficiency or dysfunction of the C1 esterase inhibitor protein. For patients managing this rare condition, understanding **what is the generic name for C1 esterase inhibitor?** is a crucial part of treatment, as the name can vary based on the drug's origin.

Understanding How does HAEGARDA work to Prevent HAE Attacks?

3 min read
Hereditary Angioedema (HAE) is a rare genetic condition, affecting an estimated 1 in 10,000 to 1 in 50,000 people, which causes unpredictable and debilitating swelling attacks. To combat this, HAEGARDA is a subcutaneous injectable medication that works to prevent these painful episodes by addressing the underlying protein deficiency.

How often do you take HAEGARDA? Understanding Your Dosing Schedule

4 min read
Clinical studies have shown that HAEGARDA can significantly reduce the frequency of hereditary angioedema (HAE) attacks. The standard regimen dictates how often do you take HAEGARDA, typically involving a twice-weekly subcutaneous injection schedule, with doses administered approximately every three to four days.