Cyklokapron is a brand of tranexamic acid, an antifibrinolytic medicine used to prevent or reduce excessive bleeding. By blocking the breakdown of fibrin clots, it helps stabilize hemostasis in settings such as heavy menstrual bleeding, dental procedures in people with hemophilia, and many surgical situations. Depending on the indication, Cyklokapron may be given as tablets or an injection. Because it influences blood clotting, it must be used under medical guidance with careful attention to dose, timing, and personal risk factors for thrombosis. Below, you’ll find evidence-based information on common uses, dosing, precautions, side effects, interactions, and practical tips for safe use.
Cyklokapron helps control bleeding by inhibiting plasminogen activation, which slows the breakdown of fibrin clots. Clinicians use it to reduce heavy menstrual bleeding, limit blood loss around surgeries (cardiac, orthopedic, ENT, gynecologic), and manage mucosal bleeding such as epistaxis. It is also used around dental procedures in individuals with hemophilia to minimize post-procedural bleeding. Depending on the clinical scenario, it may be administered orally, intravenously, or topically.
Beyond labeled uses, tranexamic acid is incorporated into protocols for trauma resuscitation and postpartum hemorrhage in many health systems and is sometimes used as adjunctive therapy in specific bleeding disorders. Its benefits are maximized when given early (for acute bleeding) and when patients are carefully assessed for thromboembolic risk. The decision to use Cyklokapron balances potential bleeding reduction with individualized safety considerations.
Dosing varies by indication, formulation, kidney function, and body weight. For heavy menstrual bleeding (HMB), a common oral regimen is 1,300 mg three times daily for up to 5 days during menses. Patients with reduced kidney function usually require lower doses or extended intervals. For perioperative bleeding reduction, typical intravenous doses range from 10–15 mg/kg at or before incision, with repeat doses or short infusions guided by procedure type and bleeding risk. In trauma protocols, a common regimen is 1 g IV as soon as possible (ideally within 3 hours of injury), followed by 1 g IV over 8 hours.
For dental extraction in hemophilia, clinicians may give 10 mg/kg IV before the procedure and continue with oral tranexamic acid (for example, 25 mg/kg or 1,000 mg three times daily) for several days. Topical approaches (e.g., soaked pledgets for nosebleeds or intraoperative irrigation) are sometimes used to focus the effect where bleeding occurs. Always follow the exact instructions from your prescriber and the product label. Take tablets with a glass of water, with or without food, and do not exceed the recommended treatment duration for your indication.
Because Cyklokapron supports clot stability, it requires careful use in people with a history of blood clots (deep vein thrombosis, pulmonary embolism, stroke), known thrombophilia, or significant cardiovascular risk. Concurrent use with combined hormonal contraceptives may further increase thrombotic risk, particularly in patients with additional risk factors; alternative strategies may be preferred. Dose adjustment is essential in renal impairment since tranexamic acid is renally cleared. Visual disturbances, including changes in color vision and blurred vision, have been reported; long-term users may be advised to undergo ophthalmic monitoring and stop treatment if visual changes occur. Rapid IV injection can cause hypotension—infuse at recommended rates. Avoid use in upper urinary tract bleeding when possible due to the risk of clot retention and obstruction. In disseminated intravascular coagulation (DIC), use only with experienced specialist oversight and appropriate anticoagulation when indicated.
Cyklokapron is contraindicated in patients with hypersensitivity to tranexamic acid, active intravascular clotting (such as ongoing DVT or PE), and a history of subarachnoid hemorrhage due to risk of cerebral ischemia. Many labels also list acquired defective color vision as a contraindication given the difficulty monitoring for ophthalmic adverse effects. Use is generally avoided in gross hematuria originating from the upper urinary tract because of the possibility of ureteral obstruction by clots. If you have ever had a blood clot, visual disturbances, or a brain bleed, inform your clinician before taking Cyklokapron.
Common side effects include gastrointestinal upset (nausea, vomiting, diarrhea, abdominal pain), headache, back pain, fatigue, and nasal or sinus symptoms. Some patients report muscle or joint aches. When given too rapidly by IV, transient hypotension and dizziness may occur; adhering to correct infusion rates reduces this risk. In long-term or high-dose settings (such as certain cardiac surgery protocols), seizures have been reported; patients with seizure history require extra caution and tailored dosing.
Serious but uncommon adverse effects include visual changes (blurred vision, impaired color vision), hypersensitivity reactions (rash, itching, swelling), and thromboembolic events (DVT, PE, stroke), especially in predisposed individuals. Any sudden chest pain, shortness of breath, unilateral leg swelling, severe headache, or visual disturbance warrants urgent medical attention. If side effects are mild, your clinician may adjust the dose or timing; persistent or severe symptoms require reassessment of the risk–benefit balance.
The most clinically important interaction involves agents that elevate thrombotic risk. Combined hormonal contraceptives, selective estrogen receptor modulators (e.g., tamoxifen, raloxifene), and other prohemostatic therapies can compound risk in susceptible patients. Using Cyklokapron with thrombolytics (such as alteplase) is pharmacologically antagonistic; tranexamic acid may reduce thrombolytic efficacy. Caution is also advised when Cyklokapron is used alongside clotting factor concentrates or activated procoagulant products. While anticoagulants and antiplatelets don’t have a direct pharmacokinetic interaction with tranexamic acid, clinicians carefully evaluate overall hemostatic balance when these agents coexist. Always provide a complete medication and supplement list to your healthcare team before starting Cyklokapron.
If you miss an oral dose, take it as soon as you remember unless it is almost time for your next scheduled dose. If it’s close to the next dose, skip the missed dose and resume your regular schedule. Do not double up to “catch up.” For indications like heavy menstrual bleeding, stick to the prescribed days of use per cycle. If you frequently forget doses, talk with your clinician about reminders or whether a different regimen might suit you better.
Symptoms of overdose may include pronounced nausea, vomiting, dizziness, low blood pressure (especially if IV), and, rarely, seizures. If you suspect an overdose or experience severe symptoms, call emergency services promptly. In the United States, you can contact Poison Control at 1-800-222-1222 for immediate guidance. Supportive care is the mainstay; because tranexamic acid is renally cleared, adequate hydration and monitoring of kidney function are important. Bring the medication container and your dosing details to the emergency department to assist rapid evaluation.
Store tablets at controlled room temperature (generally 20–25°C or 68–77°F), protected from moisture and excessive heat. Keep the medication in its original container, tightly closed, and out of reach of children and pets. For injectable Cyklokapron, follow the specific storage instructions on the label; avoid freezing and protect from light when indicated. Do not use expired products, and discard any solution that appears discolored or contains particles. Your pharmacist can advise on safe disposal.
In the U.S., Cyklokapron (tranexamic acid) is a prescription-only medicine. Although online searches may suggest ways to “buy Cyklokapron without prescription,” obtaining prescription medicines without a valid clinician order is unsafe and may be illegal, with risks of counterfeit or substandard products. A safe, legal path involves evaluation by a licensed healthcare professional who determines whether tranexamic acid is appropriate and issues a prescription with individualized dosing. HealthSouth Rehabilitation Hospital of Tallahassee offers structured, compliant access by connecting you with qualified clinicians for assessment and, when indicated, facilitating pharmacy dispensing or coordination. This approach prioritizes your safety, ensures correct indication and dose, and aligns with federal and state regulations—without cutting corners or bypassing required medical oversight.
Cyklokapron is a brand name for tranexamic acid, an antifibrinolytic medicine that helps prevent the breakdown of blood clots and reduces excessive bleeding.
It blocks the binding of plasminogen and plasmin to fibrin, stabilizing the clot and slowing fibrinolysis so bleeding is reduced without thinning the blood.
It is used for heavy menstrual bleeding, to reduce bleeding during or after surgery and dental procedures (including in people with bleeding disorders), for traumatic bleeding, nosebleeds, and in hospitals for postpartum hemorrhage. Other specialist uses exist under medical supervision.
It is available as oral tablets and as an intravenous (IV) injection. For heavy menstrual bleeding, it is taken by mouth only during days of heavy flow. In trauma and surgery, clinicians give IV doses according to protocol. Follow the exact regimen prescribed for your condition.
IV tranexamic acid starts working within minutes. For heavy menstrual bleeding, oral doses begin reducing flow the same day and can significantly lessen blood loss over that cycle.
Avoid use with active or a history of blood clots (DVT, PE), active intravascular clotting, subarachnoid hemorrhage, or known hypersensitivity. Do not use for upper urinary tract bleeding due to risk of ureteral obstruction. Use cautiously and with dose adjustment in kidney impairment. Long-term use is generally avoided in people with acquired defective color vision.
Nausea, vomiting, diarrhea, stomach discomfort, headache, sinus or nasal symptoms, and muscle or back pain can occur. Less common are visual changes (including color vision disturbances). Rare but serious effects include blood clots and seizures with high IV doses, and low blood pressure if IV is given too quickly.
Because it stabilizes clots, it can increase clot risk in susceptible people, but the absolute risk is low when used appropriately and short term. It should be avoided in those with active or recent thromboembolism and used cautiously in patients with multiple risk factors.
Combining tranexamic acid with estrogen-containing contraceptives may raise the risk of thrombosis. Discuss your personal risk and alternative contraceptive options with your clinician before combining them.
Tranexamic acid is not a reversal agent for anticoagulants. Co-use requires specialist guidance, balancing bleeding control against clot risk; do not combine without medical advice.
It is used in hospitals for postpartum hemorrhage. It is not typically used for routine pregnancy-related bleeding unless specifically indicated. Very small amounts pass into breast milk; most guidelines consider short-term use compatible with breastfeeding. Always follow medical advice.
Yes. Tranexamic acid can reduce menstrual blood loss by about 30–50% when taken during heavy days of the period. It does not affect fertility or hormone levels and is used only during bleeding days.
Yes. Topical tranexamic acid (on a pledget or gauze) can help stop epistaxis, and short oral courses may be used for recurrent nosebleeds under guidance. Seek urgent care for severe, persistent, or bilateral bleeding.
If used beyond short courses or in people with medical conditions, clinicians may monitor kidney function and, if long-term use is anticipated, visual symptoms. Seek care urgently for signs of thrombosis such as leg swelling, chest pain, or sudden shortness of breath.
If you miss a dose for heavy menstrual bleeding, take it when remembered if still needed that day; skip if near the next scheduled dose. Do not double up. Store tablets at room temperature away from moisture and heat, and keep out of reach of children.
Yes. Cyklokapron is a brand of tranexamic acid. Generic tranexamic acid products with the same strength and formulation are considered therapeutically equivalent.
Both are tranexamic acid. Lysteda is an oral brand specifically labeled for heavy menstrual bleeding with a defined 1.3 g (two 650 mg tablets) three-times-daily regimen for up to 5 days per cycle. Cyklokapron branding is often used for IV formulations and, in some regions, 500 mg tablets. Your prescriber will match the product and dose to your indication.
Both are antifibrinolytics. Tranexamic acid is more potent milligram-for-milligram and tends to have stronger evidence in trauma, surgery, and heavy menstrual bleeding. In practice, both reduce bleeding; many guidelines prefer tranexamic acid due to potency, convenience, and breadth of data.
Aminocaproic acid requires higher and more frequent dosing (often every 4–6 hours) because it is less potent. Tranexamic acid typically needs fewer daily doses. Both require dose adjustments in renal impairment.
Both can cause gastrointestinal upset and carry clot risk. Aminocaproic acid may be associated with myopathy with prolonged high doses and hypotension with rapid IV infusion. Tranexamic acid has rare seizures at high IV doses and potential visual disturbances. Overall tolerability is similar when used short term and appropriately.
Both are effective. Tranexamic acid mouthwash or soaked pledgets are widely used and well supported by evidence; aminocaproic acid mouthwash is also effective. Choice often depends on availability, clinician preference, and cost.
Tranexamic acid has robust randomized-trial evidence reducing bleeding and mortality in trauma when given early and is widely incorporated into perioperative protocols. Aminocaproic acid is less studied in these settings, so many institutions favor tranexamic acid.
Both can worsen the risk of urinary tract obstruction if bleeding originates in the upper tract by promoting clot formation in the ureter. Use for hematuria requires specialist assessment; neither is routinely used for upper tract bleeding.
Topical tranexamic acid is ideal for localized bleeding (for example, nosebleeds, dental sockets) with minimal systemic exposure. Oral or IV tranexamic acid is used for systemic indications such as heavy menstrual bleeding, surgery, trauma, or postpartum hemorrhage.
Yes. Approved generics must meet bioequivalence standards. Ensure the strength and dosing instructions match the intended regimen, and use the same formulation (tablets vs solution) as prescribed.
Substitution depends on local regulations, dosage form, and the prescriber’s intent. Because tablet strengths and labeled indications can differ, the pharmacist may need to contact the prescriber to ensure dosing equivalence before substituting.
Both reduce bleeding but act differently. Tranexamic acid is an antifibrinolytic; aprotinin is a protease inhibitor used in select cardiac surgeries in some regions with safety restrictions. For most bleeding indications, tranexamic acid is preferred due to established efficacy and safety.
Costs vary by region and insurance. Aminocaproic acid is often inexpensive per tablet but requires more tablets per day. Tranexamic acid may have higher unit cost but fewer doses and broader evidence. Total cost-effectiveness depends on indication, dosing, and coverage.
If systemic bleeding risk is low and bleeding is localized, a tranexamic acid mouthwash or soaked gauze is often sufficient and preferred. If there is a systemic bleeding disorder or ongoing oozing, clinicians may add oral tranexamic acid. Always follow the dental surgeon’s plan.