Overview of Cyklonova
| Property | Description |
|---|---|
| Active ingredient | Tranexamic Acid (TXA) |
| Form | Oral tablet and intravenous solution |
| Pharmacological class | Antifibrinolytic agent / Antihemorrhagic |
| Common use | Reducing excessive blood loss |
| Origin | Synthetic derivative (of the amino acid lysine) |
What is Cyklonova and its Pharmacological Class?
Cyklonova is a brand-name pharmaceutical preparation containing the active ingredient Tranexamic Acid (TXA). It is primarily classified as an antifibrinolytic agent, which places it within the broader group of antihemorrhagic medications used to control bleeding. The medication's classification is rooted in its highly selective pharmacological action.
Chemically, Tranexamic Acid is a pure synthetic derivative of the essential amino acid lysine. Its classification as an antifibrinolytic is recognized globally. The medication is commonly supplied by various manufacturers as both a prescription-only medicine (POM) and, in some markets, as a lower-dose Pharmacy Medicine (P).
What is the General Purpose of Tranexamic Acid?
The general purpose of the medication is to prevent the premature dissolution of blood clots, thereby helping to control or prevent instances of excessive blood loss or hemorrhage. Its core function is to stabilize fibrin clots that the body has already formed.
This antihemorrhagic effect is achieved through its selective action to inhibit fibrinolysis, which is the natural biological process where the body breaks down a clot. Tranexamic Acid is a highly potent reversible inhibitor of plasminogen activation, effectively supporting the body's natural clotting mechanisms when they are overwhelmed. This makes it clinically recognized for scenarios requiring efficient blood loss reduction.
In What Forms is Cyklonova Available?
Cyklonova is a single-ingredient product commonly available in two distinct dosage forms to accommodate various patient needs. The medication can be obtained as an oral dosage form, specifically a tablet, intended for ingestion and systemic delivery via the digestive tract. Additionally, it is available as a sterile intravenous solution for injection, which facilitates direct delivery into the bloodstream for situations requiring rapid systemic action.
Regulatory References


