Product image of Levofolinate De Calcium Zentiva (Levoleucovorin) supplied by GNH India

Levofolinate De Calcium Zentiva

Active Ingredient:
Levoleucovorin
Origin:
EU

Levofolinate De Calcium Zentiva (Levoleucovorin)

Levoleucovorin, the active ingredient in Levofolinate De Calcium Zentiva, is a folate analog presented as an injection solution for intramuscular or intravenous use. It rescues normal cells from the toxic effects of high‑dose methotrexate chemotherapy in cancer patients.

GNH India supplies Levofolinate De Calcium Zentiva as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres and pharmacies worldwide.

Manufacturer / TM Owner

Zentiva France

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Indications & Clinical Uses

Levoleucovorin is used in oncology and metabolic support to counteract antifolate chemotherapy and address folate deficiency.

  • Rescue therapy after high‑dose methotrexate: provides rapid folate replenishment to protect normal tissues.
  • Reduction of methotrexate toxicity: diminishes adverse effects such as mucositis and bone‑marrow suppression.
  • Adjunct in folate deficiency when oral supplementation is not feasible: supplies reduced folate intravenously for patients unable to take oral tablets.

How It Works

  • Levoleucovorin is a reduced form of folic acid that bypasses the dihydrofolate reductase (DHFR) step inhibited by antifolate agents such as methotrexate. By directly supplying the 5‑methyltetrahydrofolate cofactor needed for thymidylate and purine synthesis, it restores DNA replication in healthy cells while allowing the antineoplastic drug to continue acting on malignant cells.

Side Effects

Levofolinate De Calcium Zentiva may be associated with a range of adverse reactions, most of which are mild and transient.

Common Side Effects

  • Nausea: mild to moderate feeling of sickness.
  • Headache: transient mild headache.
  • Rash: localized skin erythema or itching.
  • Elevated liver enzymes: mild, reversible increase in transaminases.

Serious or Rare Side Effects

  • Anaphylactic reaction: severe allergic response with airway compromise.
  • Hypotension: sudden drop in blood pressure requiring intervention.
  • Stevens‑Johnson syndrome: severe skin detachment and mucosal involvement.

Precautions & Warnings

Before initiating Levofolinate De Calcium Zentiva, several precautionary measures should be considered to ensure safe use.

  • Assess renal function: evaluate creatinine clearance to adjust dosing if needed.
  • Monitor hepatic enzymes: check liver function tests prior to and during therapy.
  • Observe blood counts: watch for cytopenias that may indicate marrow toxicity.
  • Adjust dose in renal impairment: reduce or extend interval in patients with reduced clearance.
  • Use with caution in pregnancy: safety data are limited; weigh potential benefits against unknown risks.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Levofolinate De Calcium Zentiva can interact with other medicines, influencing efficacy or safety.

Major Interactions (Avoid)

  • Concurrent high‑dose antifolate agents (e.g., pemetrexed) without proper timing: may blunt therapeutic effect of the anticancer drug.
  • Sulfonamide antibiotics: may compete for folate pathways and reduce rescue efficiency.

Moderate Interactions (Monitor Closely)

  • Nephrotoxic drugs (e.g., aminoglycosides, NSAIDs): increase risk of renal impairment when combined.
  • Hepatotoxic agents (e.g., isoniazid, valproate): may exacerbate liver enzyme elevations.
  • Warfarin: folate supplementation can alter INR, requiring closer coagulation monitoring.
  • Vitamin B12 deficiency: may limit folate utilization, necessitating assessment.

Frequently Asked Questions

Levofolinate De Calcium Zentiva is used as a chemotherapy rescue agent to reduce the toxic effects of high‑dose methotrexate and to provide a source of reduced folate when oral supplementation is not possible, such as in patients with severe folate deficiency.

Levoleucovorin supplies the reduced folate cofactor 5‑methyltetrahydrofolate directly, bypassing the dihydrofolate reductase step that methotrexate blocks. This restores normal DNA synthesis in healthy cells while allowing methotrexate to continue targeting cancer cells.

The dose of levofolinate is individualized and set by the prescribing clinician based on the specific chemotherapy protocol, patient weight, renal function, and the degree of methotrexate exposure. No standard dose is provided here.

Safety data for levofolinate in pregnancy and lactation are limited. It should only be used when the potential benefit justifies any possible risk to the fetus or infant, and the decision must be made by the treating physician.

To order, 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 cold‑chain if needed) and import documentation.

Levofolinate (leucovorin calcium) is chemically equivalent to folinic acid and is the standard rescue agent for methotrexate toxicity. Compared with oral folic acid, it provides a reduced folate form that is active without metabolic conversion, making it more effective for rapid rescue in high‑dose settings.

Levofolinate De Calcium Zentiva should be stored at 2‑8 °C, protected from light, and must not be frozen or shaken. Use aseptic technique when preparing the injection solution, and keep the product in its original packaging until use.

Levofolinate is given by intramuscular or intravenous injection, typically shortly after high‑dose methotrexate infusion. The exact route, infusion rate, and timing are determined by the treating oncologist according to the chemotherapy protocol.

Serious risks include anaphylactic reactions, severe hypotension, and rare but life‑threatening skin conditions such as Stevens‑Johnson syndrome. Prompt medical attention is required if signs of severe allergy, sudden blood pressure drop, or extensive skin rash develop.

Levofolinate should be avoided in patients with known hypersensitivity to levoleucovorin or any component of the formulation, and it should be used with caution in individuals with severe renal or hepatic impairment. Contraindications are determined by the prescribing physician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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