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Participant ID (PID) Initials of person entering data Staff emailCONFIDENTIAL CASE REPORT FORM TRANEXAMIC ACID FOR BLEEDING Series No: 24 Palliative Care Clinical Studies Collaborative (Packs) RAPID
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To fill out the role of tranexamic acid, follow these points:
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Consult with your healthcare provider or pharmacist before starting tranexamic acid.
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Read the instructions provided with the medication carefully.
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Take the prescribed dosage as recommended by your healthcare provider.
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Usually, tranexamic acid is taken orally with water.
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If you forget a dose, take it as soon as you remember, unless it is close to the time for your next dose. In that case, skip the missed dose and continue with your regular dosing schedule.
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Do not take more than the prescribed amount of tranexamic acid.
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If you experience any side effects or have concerns, speak to your healthcare provider or pharmacist.

Who needs role of tranexamic acid?

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Tranexamic acid is typically prescribed to individuals who:
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- Suffer from excessive bleeding during heavy menstrual periods (menorrhagia).
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- Have bleeding disorders such as hemophilia.
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- Undergo surgical procedures where excessive bleeding is expected.
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- Have nosebleeds that are difficult to control.
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- Experience abnormal or heavy bleeding after childbirth.
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- Have abnormal bleeding due to certain medical conditions.
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- Are at risk of bleeding complications during dental or oral surgeries.
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Tranexamic acid is an antifibrinolytic medication that helps reduce bleeding by inhibiting the breakdown of fibrin, a protein essential for blood clotting.
Healthcare professionals, particularly those involved in prescribing or administering tranexamic acid in clinical settings, may be required to document its use and outcomes in patient records.
To fill out the role of tranexamic acid, healthcare providers must document the indications for use, dosage administered, patient response, and any adverse effects observed during treatment.
The purpose of documenting the role of tranexamic acid is to ensure appropriate use, monitor patient outcomes, and facilitate data collection for safety and efficacy assessments.
Reported information should include patient demographics, reason for administration, dose and route of administration, date and time, as well as any side effects or complications.
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