Product image of Grafalon (Anti-T Lymphocyte Immunoglobulin For Human Use, Rabbit) supplied by GNH India

Grafalon

Active Ingredient:
Anti-T Lymphocyte Immunoglobulin For Human Use, Rabbit
Origin:
EU

Grafalon (Anti-T Lymphocyte Immunoglobulin For Human Use, Rabbit)

Grafalon is a rabbit-derived anti‑T lymphocyte immunoglobulin for human use, supplied as an injectable solution for intravenous administration. The product contains polyclonal antibodies that target human T lymphocytes and is classified as an immunosuppressive agent. It is marketed in the European Union and is available by prescription only.

Manufacturer / TM Owner

Neovii Biotech Gmbh

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Indications & Clinical Uses

Grafalon is employed in clinical settings where modulation of the immune response is required. It is primarily used to reduce the risk of immune‑mediated complications following transplantation and related procedures.

  • Prevention of acute organ transplant rejection
  • Treatment of graft‑versus‑host disease (GVHD) after hematopoietic stem cell transplantation
  • Conditioning regimen component for allogeneic stem cell transplantation
  • Adjunct therapy in certain autoimmune conditions under specialist supervision

Side Effects

Side effects of Grafalon vary in frequency and severity. Common reactions are usually mild to moderate, while serious events are less frequent but require prompt medical attention.

Common

  • Fever and chills during infusion
  • Headache
  • Nausea or vomiting
  • Transient hypotension
  • Rash or mild skin erythema
  • Elevated liver enzymes

Serious

  • Severe infusion‑related reactions (anaphylaxis, bronchospasm)
  • Opportunistic infections (viral, bacterial, fungal)
  • Cytopenias (neutropenia, thrombocytopenia)
  • Malignancy risk with prolonged immunosuppression
  • Renal impairment or acute kidney injury

Precautions & Warnings

Grafalon should be used with careful monitoring and consideration of patient‑specific risk factors. Important safety points include:

  • Assess for active infections before initiating therapy
  • Monitor complete blood counts and renal function regularly
  • Avoid use in pregnant women; pregnancy category is unknown
  • Counsel patients about increased susceptibility to infections and the need for prophylactic measures
  • Consider vaccination status; live vaccines are contraindicated during treatment
  • Observe for signs of infusion reactions and be prepared to manage them

Avoid Interactions

Grafalon may interact with other medications that affect immune function or organ systems. Awareness of these interactions helps minimize adverse outcomes.

Avoid

  • Live attenuated vaccines during and shortly after therapy
  • Concurrent use of other T‑cell depleting agents without specialist guidance

Use with caution

  • Other immunosuppressants (e.g., calcineurin inhibitors, mTOR inhibitors)
  • Nephrotoxic drugs (e.g., aminoglycosides, amphotericin B)
  • Antiviral prophylaxis agents that may increase hepatic load
  • Medications that prolong QT interval, as electrolyte shifts can occur

Frequently Asked Questions

Grafalon contains polyclonal rabbit antibodies that bind to human T lymphocytes, leading to complement‑mediated lysis and depletion of T cells, thereby suppressing cellular immune responses.

Grafalon is indicated for the prevention of acute rejection in solid organ transplants such as kidney, liver, heart, and lung, when used as part of an immunosuppressive regimen.

Grafalon may be used in pediatric patients under specialist supervision, with dosing adjusted for body weight and clinical condition; specific pediatric guidelines should be consulted.

Patients should have regular monitoring of complete blood counts, renal and hepatic function tests, and clinical assessment for signs of infection or infusion reactions.

Live vaccines are contraindicated during treatment with Grafalon and for a period after therapy because of the heightened risk of vaccine‑derived infection.

Grafalon is supplied as an injectable solution and is administered intravenously, typically over several hours, under close medical supervision.

Common infusion‑related side effects include fever, chills, headache, nausea, transient low blood pressure, and mild skin rash.

Long‑term immunosuppression with Grafalon may be associated with an increased risk of certain malignancies; patients should be monitored according to oncologic surveillance guidelines.

Infusion should be stopped immediately, and emergency measures such as administration of epinephrine, antihistamines, and supportive care should be provided.

Grafalon’s pregnancy category is unknown, and it is generally avoided in pregnant or nursing women unless the potential benefit justifies the risk; consultation with a specialist is required.

Grafalon is often used in combination with other immunosuppressants as part of a transplant regimen, but dosing and timing should be coordinated by a transplant specialist to avoid excessive immunosuppression.

Grafalon is authorized for prescription use in the EU as a rabbit anti‑thymocyte globulin, classified under ATC code L04AA02.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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