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Transamin injection (tranexamic acid) is an antifibrinolytic agent used to reduce or prevent excessive bleeding. It works by inhibiting the conversion of plasminogen to plasmin, thereby stabilizing formed blood clots and preventing their breakdown (fibrinolysis).
Active ingredient: Tranexamic Acid (equivalent to 500 mg per 5 ml)
Excipients / inactive ingredients: (typical injection excipients such as water for injection, buffering agents, stabilizers) — specific excipients depend on manufacturer
Antifibrinolytic / Hemostatic agent
Sterile injection (aqueous solution) — 5 ml ampoule delivering 500 mg tranexamic acid
Transamin injection is used in conditions involving excessive bleeding or bleeding risk, such as:
To reduce bleeding during or after surgery, trauma, or in surgical procedures
Heavy menstrual bleeding (menorrhagia) when other measures are inadequate
Postpartum hemorrhage (bleeding after childbirth)
Control of bleeding in dental surgeries, hemophilia, or other bleeding disorders
To control bleeding from the gastrointestinal tract or other internal bleeding settings (depending on clinical decision)
The dose and frequency depend on the severity of bleeding, patient condition, and medical advice.
In many clinical settings, the injection is administered intravenously (IV) slowly or intramuscular (IM) as needed under supervision.
The dose may be repeated or maintained as per the physician’s protocol.
Symptoms may include nausea, vomiting, diarrhea, hypotension, seizures in severe cases
Management should be supportive and symptomatic, with monitoring of vital signs and appropriate medical care.
Because injection is administered in clinical settings, “missed dose” is not commonly applicable to patient self-administration.
Any discrepancy in dosing should be handled by the treating healthcare provider.
Administer slow IV injection or IM under aseptic conditions.
IV route is preferred in many instances to ensure controlled delivery and reduce risks.
The injection should be given slowly to avoid hemodynamic or adverse effects.
Monitor patient during and after injection for reactions and bleeding control.
Known hypersensitivity to tranexamic acid or any components of the formulation
Active thromboembolic disease (e.g. deep vein thrombosis, pulmonary embolism) or history of clotting disorders
Hematuria (significant blood in urine) or bleeding in urinary tract may worsen clots in unwanted places
Pregnancy and breastfeeding: use only if benefits outweigh risks (caution)
Patients with a history of seizures should take caution, as tranexamic acid has been associated with risk in some reports
Common / Less Serious:
Dizziness, lightheadedness
Skin rash, itching or local reactions
Rare / Serious:
Thromboembolic events (blood clots) in predisposed patients
Changes in color vision or visual disturbances
Allergic reactions (swelling, breathing difficulty)
Use caution in patients with renal impairment, history of clotting disorders, cardiovascular disease
Monitor kidney function, clotting status, and signs of thrombosis
In prolonged therapy, observe for adverse effects
Avoid combining with other agents that increase clotting risk unless under close supervision
Use the lowest effective dose for shortest possible duration
Inform physicians/dentists of use of tranexamic acid prior to surgery or invasive procedures
In patients with seizure history, caution is advised
Use with combined hormonal contraceptives or estrogens may increase clotting risk
Concurrent use with oral anticoagulants or thrombolytics requires caution and medical supervision
Other agents affecting clotting or fibrinolysis may interact (increasing or reducing effect)
Store at room temperature in a dry place, protect from direct sunlight
Do not freeze
Use before expiry date
Dispose of unused or expired ampoules following biomedical waste guidelines
Tranexamic acid is not a controlled narcotic, but it is a prescription medicine that must be used under medical supervision
Administer slowly when given IV to reduce adverse reactions
Monitor for signs of clotting or thrombosis, especially in high-risk patients
Avoid use in patients with thrombotic history
Use minimal effective dose for shortest time
Always consult a physician before using during pregnancy or lactation
Ensure proper renal function before use
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