Product image of Lederfoline (Folinic Acid) supplied by GNH India

Lederfoline

Active Ingredient:
Folinic Acid
Origin:
EU

Lederfoline (Folinic Acid)

Folinic acid, the active ingredient in Lederfoline, is a folate analog (antimetabolite) presented as an oral formulation for prescription use. It is employed to reduce toxicity of fluoropyrimidine chemotherapy, to rescue patients after high‑dose methotrexate, and to treat folate deficiency in appropriate clinical settings.

GNH India supplies Lederfoline as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Pfizer Holding France

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Indications & Clinical Uses

Lederfoline is a folate analog used in oncology and metabolic support pathways. It addresses several clinically recognised conditions:

  • Adjunct to fluoropyrimidine chemotherapy: reduces toxicity and supports efficacy of 5‑FU or capecitabine regimens.
  • Rescue after high‑dose methotrexate: restores reduced folate pools to prevent severe myelosuppression.
  • Treatment of folate deficiency: replenishes folate stores in patients with inadequate dietary intake or malabsorption.

How It Works

  • Folinic acid is the reduced form of folic acid that bypasses dihydrofolate reductase inhibition. It directly replenishes intracellular reduced folate pools, enabling normal thymidylate and purine synthesis. By restoring these pathways, it mitigates the cytotoxic effects of antifolate agents such as methotrexate and enhances the therapeutic index of fluoropyrimidine chemotherapy.

Side Effects

Lederfoline may cause a range of adverse reactions. Patients should be aware of both common and serious possibilities.

Common Side Effects

  • Nausea: mild to moderate gastrointestinal upset.
  • Diarrhea: loose stools that may require hydration.
  • Rash: skin erythema or mild itching.
  • Headache: transient cranial discomfort.
  • Fatigue: generalised tiredness.
  • Mild elevation of liver enzymes.

Serious or Rare Side Effects

  • Allergic reactions: urticaria, angioedema, or anaphylaxis.
  • Severe skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Renal dysfunction: acute kidney injury in susceptible individuals.
  • Hepatic toxicity: marked transaminase rise or hepatitis.
  • Bone marrow suppression: pancytopenia or severe neutropenia.
  • Thromboembolic events: rare clot formation.

Precautions & Warnings

Before prescribing Lederfoline, clinicians should consider several safety measures.

  • Renal function: assess baseline creatinine clearance and monitor during therapy.
  • Hepatic function: evaluate liver enzymes and adjust use if significant impairment exists.
  • Concurrent methotrexate: avoid overlapping high‑dose schedules to prevent additive toxicity.
  • Pregnancy: use only when the potential benefit justifies the potential risk to the fetus.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Lederfoline can interact with several medicines; awareness of the interaction level guides management.

Major Interactions (Avoid)

  • High‑dose methotrexate: concurrent use may exacerbate toxicity.
  • Antifolate agents (e.g., pemetrexed): antagonistic effect reduces efficacy of both drugs.
  • Leucovorin rescue timing: improper timing can diminish intended protective effect.

Moderate Interactions (Monitor Closely)

  • Nephrotoxic drugs (e.g., cisplatin): monitor renal parameters closely.
  • Hepatotoxic agents (e.g., azathioprine): observe liver function tests regularly.
  • Vitamin B12 deficiency: may alter folate metabolism and response to therapy.

Frequently Asked Questions

Lederfoline contains folinic acid and is used as an adjunct to fluoropyrimidine chemotherapy to lessen toxicity, as a rescue therapy after high‑dose methotrexate to restore folate pools, and to treat documented folate deficiency in patients who need metabolic supplementation.

Folinic acid is the biologically active, reduced form of folic acid. It bypasses the dihydrofolate reductase block created by antifolate drugs, directly replenishing intracellular reduced folate, which supports DNA synthesis and repair, thereby protecting normal cells and enhancing the effectiveness of certain chemotherapies.

The prescribed dose of Lederfoline is individualized by the treating physician based on the specific indication, patient weight, renal and hepatic function, and concurrent therapies. Dosage regimens are not standardized and must follow the prescriber's instructions.

Safety data for folinic acid in pregnancy and lactation are limited. It should only be used when the potential benefit to the mother outweighs any possible risk to the fetus or infant, and the decision must be made by a qualified healthcare professional.

To order Lederfoline, submit an enquiry on the product page at gnhindia.com specifying the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including any cold‑chain requirements) and the necessary import documentation.

Lederfoline (folinic acid) differs from standard folic acid because it is already in the reduced, biologically active form. This allows it to bypass dihydrofolate reductase inhibition, making it effective as a rescue agent after antifolate chemotherapy, whereas regular folic acid does not provide the same rapid cellular protection.

Lederfoline should be stored at room temperature, below 25 °C, in its original packaging to protect it from moisture and light. Keep the container tightly closed and out of reach of children.

Lederfoline is administered orally. The tablet or capsule should be swallowed whole with a glass of water, unless the prescriber advises otherwise. It can be taken with or without food, but consistency with meals may help reduce gastrointestinal discomfort.

Serious risks include severe allergic reactions such as anaphylaxis, rare but life‑threatening skin conditions like Stevens‑Johnson syndrome, significant renal or hepatic impairment, and profound bone‑marrow suppression leading to pancytopenia. Patients should be monitored closely for any of these events.

Lederfoline is contraindicated in patients with known hypersensitivity to folinic acid or any excipients in the formulation. It should also be avoided in individuals receiving overlapping high‑dose antifolate therapy without appropriate timing adjustments, and in patients with severe renal or hepatic failure unless specifically directed by a specialist.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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