Product image of Leucovorine (Calcium Folinate Pentahydrate) supplied by GNH India

Leucovorine

Active Ingredient:
Calcium Folinate Pentahydrate
Origin:
EU

Leucovorine (Calcium Folinate Pentahydrate)

Calcium folinate, the active ingredient in Leucovorine, is a folate analog presented as an oral formulation for prescription use. It is employed to counteract the effects of antifolate chemotherapy and to correct folate deficiency in patients receiving cancer treatment.
GNH India supplies Leucovorine as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres and pharmacies worldwide.

Manufacturer / TM Owner

Sandoz B.V.

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Indications & Clinical Uses

Leucovorine is used in oncology and supportive care to address folate‑related pathways.

  • High‑dose methotrexate rescue: restores normal cell replication after methotrexate‑induced toxicity.
  • 5‑Fluorouracil adjunct: enhances efficacy of 5‑FU‑based regimens in colorectal cancer.
  • Folate deficiency prevention: supplies reduced folate to patients with low folate stores.
  • Antifolate toxicity mitigation: reduces adverse effects of drugs that inhibit dihydrofolate reductase.

How It Works

  • Calcium folinate provides a reduced folate cofactor that bypasses dihydrofolate reductase inhibition, allowing the synthesis of thymidylate and purine nucleotides to continue. By supplying this active folate form, it restores DNA synthesis in normal cells while antifolate agents remain active against tumor cells, thereby reducing chemotherapy‑related toxicity.

Side Effects

Leucovorine may cause a range of adverse reactions, most of which are mild and reversible.

Common Side Effects

  • Nausea: mild to moderate stomach upset.
  • Diarrhoea: loose stools that resolve with continued therapy.
  • Transient liver enzyme elevation: mild increase in ALT/AST.
  • Rash: mild skin erythema or itching.

Serious or Rare Side Effects

  • Severe hypersensitivity: anaphylaxis or angioedema requiring immediate medical attention.
  • Hematologic abnormalities: rare cases of pancytopenia.
  • Renal impairment: occasional acute kidney injury.
  • Pulmonary toxicity: rare interstitial pneumonitis.

Precautions & Warnings

Before prescribing Leucovorine, clinicians should consider patient‑specific factors and monitor for potential complications.

  • Renal function: assess creatinine clearance before and during therapy.
  • Hepatic function: monitor liver enzymes regularly.
  • Pregnancy status: evaluate risk versus benefit if use is contemplated during pregnancy.
  • Concomitant antifolates: avoid overlapping use with other folate antagonists.
  • Allergies: check for known hypersensitivity to calcium folinate or excipients.
  • Store at ambient temperature: keep below 25°C, in the original container, protected from moisture and direct sunlight.

Avoid Interactions

Leucovorine can influence the activity of several co‑administered medicines.

Major Interactions (Avoid)

  • Methotrexate high‑dose regimens: may reduce methotrexate efficacy if given simultaneously.
  • Trimethoprim‑sulfamethoxazole: can increase risk of bone marrow suppression.

Moderate Interactions (Monitor Closely)

  • Phenytoin: may alter folate metabolism, requiring dose adjustment.
  • Anticonvulsants (e.g., carbamazepine, phenobarbital): may increase folate turnover.
  • Oral contraceptives: potential reduction in folate levels, monitor for deficiency symptoms.

Frequently Asked Questions

Leucovorine is prescribed as a folate analog to rescue patients after high‑dose methotrexate therapy, to support treatment with 5‑fluorouracil in certain solid tumours, and to prevent or correct folate deficiency caused by chemotherapy.

Calcium folinate supplies a reduced form of folate that bypasses the block created by dihydrofolate reductase inhibitors. This restores the synthesis of nucleotides needed for DNA replication in normal cells, reducing the toxic effects of antifolate chemotherapy.

The dose of Leucovorine is individualized by the prescribing clinician based on the specific indication, patient weight, renal function, and concurrent chemotherapy regimen. Only a qualified healthcare professional should determine the appropriate dosing schedule.

Safety data for Leucovorine in pregnancy and lactation are limited. It should only be used if the potential benefit justifies any possible risk to the fetus or infant, and the decision must be made by a qualified obstetrician‑oncologist.

To place an order, submit an enquiry on the Leucovorine 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 required import documentation.

Leucovorine (calcium folinate) is a reduced folate that directly bypasses dihydrofolate reductase inhibition, similar to leucovorin. Compared with folic acid, it provides a more immediate biochemical rescue, making it the preferred choice for high‑dose methotrexate and antifolate toxicity management.

Leucovorine should be stored at ambient temperature, below 25 °C, in its original packaging. Keep the product away from moisture, direct sunlight and sources of heat to maintain stability.

Leucovorine is administered orally as a tablet or liquid preparation, according to the prescriber’s instructions. It may be given with or without food, but patients should follow the specific guidance provided by their healthcare professional.

Serious risks include severe hypersensitivity reactions such as anaphylaxis, rare cases of pancytopenia, acute kidney injury, and interstitial pneumonitis. Patients should be monitored for signs of these events and seek immediate medical attention if they occur.

Leucovorine is contraindicated in patients with known hypersensitivity to calcium folinate or any of its excipients. It should also be avoided in individuals receiving overlapping high‑dose antifolate therapy without appropriate medical supervision.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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