Tranexamic Acid competitively inhibits the activation of plasminogen by binding to its kringle domain, thereby preventing its conversion to plasmin. Plasmin is responsible for breaking down fibrin clots, fibrinogen, and several coagulation factors. By inhibiting plasmin formation and activity, Tranexil 500 mg effectively reduces fibrinolysis and controls bleeding.
After oral administration, Tranexamic Acid is rapidly absorbed, reaching peak plasma concentration within 2–3 hours. Approximately 40% of the oral dose and about 45% of the intravenous dose are excreted unchanged in the urine within 24 hours.
রেজিস্টার্ড চিকিৎসকের পরামর্শ অনুযায়ী ঔষধ সেবন করুন
In Medicine:
Prophylaxis and treatment of hemoptysis
Digestive tract hemorrhages
Hemorrhagic syndromes in leukemia, cirrhosis, hemophilia
Thrombocytopenic purpura
Bleeding associated with thrombolytic therapy and blood transfusion
In Surgery:
Prevention and control of bleeding during and after all types of surgery
Particularly useful in pulmonary, cardiovascular, and abdominal surgeries
Management of post-operative and traumatic shock-related hemorrhage
In Urology:
Prophylaxis and treatment of bleeding in prostatic, vesical, and renal surgery
Management of hematuria
In Obstetrics & Gynecology:
Postpartum and puerperal hemorrhage
Functional menorrhagia and metrorrhagia
IUD-induced menorrhagia
Bleeding due to cervical conization
Hyperfibrinolysis associated with abruptio placentae and premature placental detachment
In Otorhinolaryngology:
Tonsillectomy-related bleeding
Epistaxis
Bleeding during ENT surgical procedures
In Stomatology & Dental Surgery:
Prevention and treatment of bleeding during tooth extraction and maxillofacial surgery, especially in patients with coagulopathies
In Oncology (Supportive Therapy):
Reduction of bleeding during surgical interventions
Promotion of fibrin capsule formation to inhibit ovarian tumor growth
Regression of carcinoma-associated ascites
General Adult Dose:
500–1000 mg orally, three times daily
Prophylaxis:
0.5–1 g orally per day
500 mg via intravenous or intramuscular route
Therapeutic Use:
1–3 g orally per day in divided doses
In severe cases, initial slow intravenous injection of 500 mg followed by oral therapy
Special Indications:
Menorrhagia: 1–1.5 g orally, 3–4 times daily for 3–4 days
Epistaxis: 1.5 g orally, three times daily for 4–10 days
Prostatectomy: 5–10 ml IV every 8 hours for 3 days, then oral therapy
Dental surgery in coagulopathies: IV and oral dosing based on body weight
Children:
Prophylaxis: 5–10 mg/kg/day orally
Treatment: 10–20 mg/kg/day orally; IV dose 10 mg/kg
Elderly: No dose adjustment unless renal impairment is present
Incompatible with penicillin-containing solutions
Antagonized by thrombolytic agents such as streptokinase and urokinase
Increased risk of thrombosis with estrogen-containing drugs
Direct admixture with whole blood during transfusion should be avoided
Hypersensitivity to Tranexamic Acid
Active thromboembolic disorders
Arterial or venous thrombosis
Endocavitary hemorrhage
Severe renal failure
Tranexil 500 mg is generally well tolerated. Possible adverse effects include:
Nausea, diarrhea, gastric discomfort
Fatigue and dizziness
Skin rash, itching, redness
Nasal congestion and conjunctival irritation
Rare cases of postural hypotension
Tranexamic Acid crosses the placenta, and clinical data in pregnancy are limited. Use during pregnancy should be avoided unless clearly necessary. The drug is excreted in breast milk in very small amounts and is unlikely to affect the infant at therapeutic doses.
Use only in confirmed hyperfibrinolytic states
Adjust dosage in patients with renal impairment
Use cautiously in patients with cardiovascular or hepatic disease
Reduce dose in isolated hematuria to avoid urinary tract clot formation
Store in a dry place at 15–30°C, protected from light, and keep out of reach of children.
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