Product image of Gordox (Aprotinin) supplied by GNH India

Gordox

Active Ingredient:
Aprotinin
Origin:
EU

Gordox (Aprotinin)

Gordox is an injectable solution that contains the active ingredient aprotinin. It is supplied in a sterile liquid form for intravenous administration. As a serine protease inhibitor, Gordox belongs to the antifibrinolytic therapeutic class and is marketed in the European Union as a prescription‑only medication.

Manufacturer / TM Owner

Gedeon Richter Plc.

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Indications & Clinical Uses

Gordox is indicated for the prevention of excessive bleeding during certain surgical procedures, particularly cardiac surgery where control of fibrinolysis is critical.

  • Reduces intra‑operative blood loss in coronary artery bypass grafting.
  • Helps maintain hemostasis during heart valve replacement.
  • Used as an adjunct in complex cardiac reconstructive surgeries.
  • May be employed when rapid clot stabilization is required.
  • Supports surgical teams in managing patients with high fibrinolytic activity.

Side Effects

Aprotinin can cause a range of adverse reactions, varying from mild to severe. Monitoring patients for signs of these effects is part of standard clinical practice.

Common

  • Transient hypotension or hypertension.
  • Nausea, vomiting, or mild gastrointestinal discomfort.
  • Elevated serum creatinine levels indicating renal stress.
  • Mild allergic skin reactions such as rash or pruritus.

Serious

  • Acute renal failure or significant decline in kidney function.
  • Severe hypersensitivity reactions, including anaphylaxis.
  • Thromboembolic events such as deep vein thrombosis or pulmonary embolism.

Precautions & Warnings

Before administering Gordox, clinicians should evaluate patient history and current clinical status to mitigate potential risks.

  • Assess renal function; avoid use in patients with severe impairment.
  • Review any known hypersensitivity to aprotinin or related proteins.
  • Monitor coagulation parameters and platelet counts during treatment.
  • Use cautiously in patients with a history of cardiovascular disease.
  • Consider alternative antifibrinolytics if the patient is pregnant, as safety data are limited.

Avoid Interactions

Gordox may interact with other medications that affect coagulation, renal function, or immune response. Awareness of these interactions helps optimize patient safety.

Avoid

  • Concurrent use with other potent antifibrinolytic agents (e.g., tranexamic acid) without specialist guidance.
  • Simultaneous administration of nephrotoxic drugs such as aminoglycosides.
  • Combination with medications that significantly prolong bleeding time, like high‑dose aspirin or clopidogrel.

Use with caution

  • Concomitant therapy with ACE inhibitors or ARBs, which may affect renal perfusion.
  • Co‑administration of immunosuppressants that could alter hypersensitivity risk.
  • Overlapping use with other serine protease inhibitors, requiring close monitoring of coagulation status.

Frequently Asked Questions

Aprotinin inhibits serine proteases such as plasmin, kallikrein, and trypsin, which reduces fibrinolysis and helps stabilize blood clots during surgery.

Gordox is primarily used to prevent excessive bleeding during cardiac surgeries, including coronary artery bypass grafting and heart valve replacement.

Gordox is supplied as an injectable solution and is administered intravenously under the supervision of a qualified healthcare professional.

No, Gordox is classified as a prescription‑only medication and must be prescribed by a licensed clinician.

Common side effects include transient changes in blood pressure, mild nausea or vomiting, temporary elevation of serum creatinine, and mild skin reactions such as rash.

Serious reactions may involve acute renal failure, severe allergic responses including anaphylaxis, and thromboembolic events like deep vein thrombosis.

Patients with severe renal impairment should be evaluated carefully, and the use of Gordox may be avoided or require close monitoring of kidney function.

Concurrent use with other potent antifibrinolytics such as tranexamic acid is generally avoided unless specifically directed by a specialist.

Clinicians should monitor blood pressure, renal function (serum creatinine), coagulation parameters, and watch for any signs of hypersensitivity.

The pregnancy safety category for aprotinin is unknown; therefore, it should be used during pregnancy only if the potential benefit justifies the potential risk.

If an allergic reaction occurs, the infusion should be stopped immediately, and appropriate emergency treatment, such as antihistamines or epinephrine, should be administered.

Aprotinin may interact with nephrotoxic drugs, other anticoagulants, and medications that affect renal perfusion, requiring dose adjustments or heightened monitoring.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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