This information is for educational purposes only. It is not intended as medical advice. Always consult a qualified healthcare professional.
Adzynma — Description, Dosage, Side Effects | PillsCard
Rx
Adzynma
500 IU, Proszek i rozpuszczalnik do sporządzania roztworu do wstrzykiwań
INN: rADAMTS13
Data updated: 2026-04-13
Available in:
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Form
Proszek i rozpuszczalnik do sporządzania roztworu do wstrzykiwań
Dosage
500 IU
Route
dożylna
Storage
—
About This Product
User Reviews
Reviews reflect personal experiences and are not medical advice. Always consult your doctor.
Manufacturer
Takeda Manufacturing Austria AG (Austria)
Composition
rADAMTS13 100 IU/ml
ATC Code
B01AD13
Source
URPL
Apadamtase alfa (ADAMTS13) is an enzyme belonging to the group of plasma zinc metalloproteinases. This enzyme is responsible for cleaving large multimeric complexes of von Willebrand factor involved in the coagulation process. The breakdown of large von Willebrand factor multimer clusters reduces the ability of this factor to bind to platelets and form microthrombi. The role of recombinant ADAMTS13 is to replace the deficient endogenous enzyme and reduce platelet consumption in the patient, ultimately protecting against the development of thrombocytopenia.
The medicinal product is administered intravenously; however, peak ADAMTS13 enzymatic activity was observed one hour after administration of the active substance.
The medicinal product has a protein structure and is therefore degraded into smaller peptides and amino acids, which are subsequently recycled by the body.
The approximate half-life of the active substance is approximately 48 hours.
⚠️ Warnings
Hypersensitivity reactions of an allergic nature, including anaphylactic reactions, may occur during treatment. Patients should be informed of possible early symptoms, such as tachycardia, chest tightness, wheezing and/or sudden dyspnoea, hypotension, generalised urticaria, pruritus, rhinitis and conjunctivitis, angioedema, somnolence, nausea, vomiting, paraesthesia, or anxiety. In some cases, these symptoms may progress to anaphylactic shock. In the event of severe allergic reactions, administration of the medicinal product must be discontinued immediately and appropriate supportive treatment initiated. As with other therapeutic proteins, the use of apadamtase alfa carries a potential risk of immunogenicity. Patients may develop antibodies directed against rADAMTS13, which may lead to a diminished clinical response to treatment. If the presence of antibodies is suspected and therapy is ineffective, alternative treatments should be considered.