Ryplazim, with the generic name plasminogen, human-tvmh, is an injectable medication used to treat plasminogen deficiency type 1 (hypoplasminogenemia). Ryplazim was approved by the U.S. Food and Drug Administration (FDA) on June 4, 2021. This approval marked a significant milestone as Ryplazim is the first therapy approved for treating plasminogen deficiency type 1, providing an essential treatment option for patients suffering from this rare disorder.
Ryplazim is specifically indicated to increase the blood levels of plasminogen in individuals with plasminogen deficiency type 1. The medication is administered directly into the bloodstream, either in a healthcare facility or at home under appropriate supervision.
The administration of Ryplazim involves:
Allergic Reactions: Patients should not use Ryplazim if they have had severe reactions to it or any other plasminogen-containing products. Allergic reactions can include trouble breathing, chest tightness, swelling, itching, and rash.
Pregnancy and Breastfeeding: It is not known if Ryplazim affects pregnancy or passes into breast milk. Patients should inform their healthcare provider if they are pregnant, planning to become pregnant, or breastfeeding.
Bleeding Risks: Ryplazim may worsen or prolong bleeding. It is crucial to seek emergency care if experiencing significant or persistent bleeding.
Antibody Formation: The body may produce antibodies against Ryplazim, which could reduce its effectiveness. Regular monitoring by healthcare providers is necessary.
Common side effects of Ryplazim include:
Patients should immediately stop treatment and contact their healthcare provider if they experience symptoms of a severe allergic reaction or significant side effects.
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