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

Lederfolin

Active Ingredient:
Folinic Acid
Origin:
EU

Lederfolin (Folinic Acid)

Folinic Acid, the active ingredient in Lederfolin, is a folate analog presented as an oral formulation for oral use. It is employed as a rescue agent to mitigate toxicity from high‑dose methotrexate and other antifolate chemotherapies, and to treat folate deficiency.

GNH India supplies Lederfolin as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres, and pharmacies worldwide, ensuring consistent quality and regulatory compliance while providing reliable logistics for global distribution.

Manufacturer / TM Owner

Pfizer S.L.

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Indications & Clinical Uses

Lederfolin is a folate analog used in clinical situations where folate metabolism is compromised or where antifolate drugs pose a toxicity risk.

  • Rescue therapy after high‑dose methotrexate: restores folate‑dependent DNA synthesis and reduces methotrexate‑induced toxicity.
  • Adjunct in cancer chemotherapy regimens: supports normal cell recovery during antifolate‑based treatment.
  • Prevention of toxicity from antifolate drugs: mitigates adverse effects of agents such as pemetrexed.
  • Treatment of folate deficiency: replenishes reduced folate stores in patients with inadequate dietary intake or malabsorption.

How It Works

  • Folinic Acid provides a reduced form of folic acid that bypasses the dihydrofolate reductase step, directly entering the folate cycle. This restores the synthesis of thymidine and purine nucleotides and supports methylation reactions, thereby counteracting the inhibition caused by antifolate agents and correcting folate deficiency at the cellular level.

Side Effects

Lederfolin is generally well tolerated, but adverse reactions can occur.

Common Side Effects

  • Nausea
  • Vomiting
  • Diarrhea
  • Mild rash or skin erythema
  • Headache
  • Transient fever

Serious or Rare Side Effects

  • Anaphylactic or severe allergic reactions
  • Stevens‑Johnson syndrome or toxic epidermal necrolysis
  • Hepatotoxicity with elevated liver enzymes
  • Pancytopenia or severe bone‑marrow suppression
  • Acute renal failure in predisposed patients

Precautions & Warnings

Before initiating Lederfolin, clinicians should consider several safety measures.

  • Renal function assessment: adjust dosing in patients with impaired clearance.
  • Hepatic monitoring: observe liver enzymes during prolonged therapy.
  • Concomitant methotrexate: ensure appropriate timing to avoid antagonism.
  • Known hypersensitivity: avoid use in patients with documented folinic acid allergy.
  • Pregnancy and lactation: use only if potential benefit justifies potential risk, as safety data are limited.
  • Store at below 25°C: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Lederfolin may interact with several medications that affect folate pathways or renal clearance.

Major Interactions (Avoid)

  • High‑dose methotrexate: concurrent use without proper scheduling can reduce rescue efficacy.
  • Pemetrexed: may diminish antifolate activity, requiring dose adjustment.
  • Trimethoprim‑sulfamethoxazole: can increase risk of folate depletion.

Moderate Interactions (Monitor Closely)

  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): may impair renal elimination of folinic acid.
  • Proton‑pump inhibitors: potential reduction in oral absorption.
  • Phenytoin and other enzyme‑inducing antiepileptics: may increase folinic acid metabolism.
  • Vitamin B12 deficiency: concurrent supplementation may be needed for optimal effect.

Frequently Asked Questions

Lederfolin contains folinic acid and is used as a rescue agent to reduce toxicity from high‑dose methotrexate and other antifolate chemotherapy drugs, as well as to treat patients with folate deficiency.

Folinic acid is a reduced form of folic acid that bypasses the dihydrofolate reductase step, directly entering the folate cycle. This restores nucleotide synthesis and methylation reactions that are blocked by antifolate agents, helping normal cells recover.

The dose of Lederfolin is determined by the prescribing clinician based on the specific indication, patient weight, renal and hepatic function, and concurrent therapies. Dosage regimens are individualized and should follow the prescriber’s instructions.

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

To order Lederfolin, 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 and any necessary import documentation.

Unlike standard folic acid, folinic acid is already in a reduced form and does not require activation by dihydrofolate reductase. This makes it effective as a rescue agent for antifolate toxicity, whereas regular folic acid cannot reverse the effects of drugs like methotrexate.

Lederfolin should be stored at below 25 °C in its original packaging, protected from moisture and direct sunlight. Maintaining these conditions helps preserve the product’s stability and potency throughout its shelf life.

Lederfolin is administered orally, typically as tablets or capsules, and should be taken according to the prescriber’s schedule. It may be given with or without food, depending on the specific clinical protocol.

Serious risks include severe allergic reactions such as anaphylaxis, life‑threatening skin conditions like Stevens‑Johnson syndrome, hepatotoxicity, and bone‑marrow suppression. Patients should be monitored closely for any signs of these reactions.

Lederfolin is contraindicated in individuals with known hypersensitivity to folinic acid or any of its excipients. Caution is also advised for patients with severe renal or hepatic impairment, and it should be avoided in pregnancy unless clearly indicated by a physician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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