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Brand Name :
Cyklokapron
Synonyms :
tranexamic acid injection
Class :
Coagulation modifiers, Miscellaneous
Dosage Forms & Strengths
Solution for injection
100mg/mL
Intravenous (IV)
1 g in 10 mL (100 mg/mL) Intravenous (IV) at 1 ml/minute (i.e., given over 10 minutes)
If bleeding does not stop after 30 minutes or if bleeding starts again within 24 hours of finishing the first dose, another 1 g IV dose will be given
Dosage forms and strengths
Solution
100mg/mL
Refer to the adult dosing regimen
Actions and Spectrum
tranexamic acid is an antifibrinolytic agent which blocks the action of plasmin, a substance which is accountable for the breakdown of blood clots. It is used in both the treatment and prevention of bleeding which is because of various medical conditions or procedures like heavy menstrual bleeding in women as well as surgery, trauma and few types of cancers. The tranexamic acid injection can thus also help with the preventing of bleeding in haemophilia patients especially if they are undergoing a tooth extraction or other surgical procedure.
Frequency not defined
Visual abnormalities
Nausea
Diarrhea
Hypotension
Vomiting
Anaphylaxis
Black Box Warning
Due to the higher risk of thrombosis including conditions of myocardial infraction, stroke, pulmonary embolism, and deep vein thrombosis (DVT). Injections of tranexamic acid that produce the black box warning which indicates using the minimal dose for the minimum period are possible.
Contraindication/Caution:
Contraindication:
Color vision disturbances
Hypersensitivity
Caution
Renal impairment
Hepatic impairment
Pregnancy/Lactation
Pregnancy consideration: US FDA pregnancy category: Not assigned
Lactation: It is not known whether tranexamic acid is excreted in human milk
Pregnancy category:
Pharmacology
tranexamic acid is an antifibrinolytic agent which functions by preventing the fibrinolysation of the clots. It moderates the activation of plasmin and thereby prevents the conversion of its major substrate plasminogen into plasmin that degrade fibrin clots. It can also occupy the lysine-binding sites on plasminogen and plasmin and consequently prevent them from binding to fibrin and thereby breaks the clots.
Pharmacodynamics:
An antifibrinolytic drug named tranexamic acid works by inhibiting the breakdown of blood clots. Fibrin Degradation products achieved that point by competitively averting plasmin activity and plasmin activation, both of which steps high in fibrinolysis. Consequently, bleeding is mitigated and the effectiveness of the clots are improved as well. Tranexamic acid is different from some medicines, which work through direct impact on other coagulation factors or aggregation of platelets.
Pharmacokinetics:
Absorption
It is rapidly cleared from the plasma after intravenous administration with peaks of plasma concentrations between 5 and 15 minutes time.
Distribution
It is widely distributed throughout the body, with a volume of distribution of approximately 10 L. The drug crosses the placenta and is also excreted into breast milk
Metabolism
tranexamic acid is degraded secondarily by the liver and is mostly excreted unchanged via the urine. Unlike the parent drugs crystalloids and colloids, the drug may be partially metabolized to an N-acetylated derivative.
Elimination and excretion
Around 90% of a tranexamic acid dose excreted in urine, practically unchanged within the first 24 hours after administration. The drug is rapidly cleared from the system, with a half-life of around 3 hours in patients with normal kidney function.
Administration
It is administered intravenously
Patient information leaflet
Generic Name: tranexamic acid injection
Pronounced: [ tran-ex-AM-ik-AS-id]
Why do we use tranexamic acid injection?
Tranexamic acid has the ability of reducing the excessive bleeding in women during the menstrual period. It may be suitable for teenage girls yet it is not advisable to use it before the first period.