Product image of Leucovorin Teva (Calcium Folinate) supplied by GNH India

Leucovorin Teva

Active Ingredient:
Calcium Folinate
Origin:
EU

Leucovorin Teva (Calcium Folinate)

Calcium folinate, the active ingredient in Leucovorin Teva, is a folate analog presented as a sterile solution for epidural, intrabursal, intracoronary use. It is employed to rescue patients from methotrexate toxicity, support cancer chemotherapy regimens, and treat folate deficiency in clinical settings.
GNH India supplies Leucovorin Teva as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Teva Pharma B.V.

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Indications & Clinical Uses

Leucovorin Teva is a folate analog used in several therapeutic pathways related to folate metabolism and chemotherapy support.

  • Rescue from methotrexate toxicity: restores normal folate pools and reduces toxic effects of high‑dose methotrexate.
  • Adjunct in cancer chemotherapy: enhances the efficacy of certain antimetabolite regimens by stabilising DNA synthesis.
  • Treatment of folate deficiency: supplies reduced folate to patients with inadequate dietary intake or malabsorption.

How It Works

  • Calcium folinate provides a reduced form of folic acid that bypasses dihydrofolate reductase inhibition. By entering the folate cycle downstream of the blocked step, it restores tetrahydrofolate pools, enabling normal purine and pyrimidine synthesis and supporting DNA replication in healthy cells while allowing antimetabolite drugs to target malignant cells.

Side Effects

Leucovorin Teva is generally well tolerated, but adverse reactions can occur.

Common Side Effects

  • Nausea: mild to moderate gastrointestinal upset.
  • Diarrhea: loose stools, often transient.
  • Rash: skin erythema or itching.
  • Fever: low‑grade temperature elevation.
  • Headache: mild to moderate head discomfort.
  • Elevated liver enzymes: transient increase in hepatic transaminases.

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction requiring immediate medical attention.
  • Severe skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Hemolytic anemia: destruction of red blood cells, especially in patients with G6PD deficiency.
  • Acute renal failure: sudden loss of kidney function, rare but serious.
  • Thromboembolic events: blood clot formation in veins or arteries.
  • Hypersensitivity pneumonitis: inflammatory lung condition following exposure.

Precautions & Warnings

When handling Leucovorin Teva, consider the following precautions to ensure patient safety and product integrity.

  • Assess renal function: adjust use in patients with impaired kidney clearance.
  • Monitor hepatic enzymes: watch for liver function changes during therapy.
  • Evaluate for G6PD deficiency: avoid use in individuals prone to hemolysis.
  • Observe for allergic reactions: discontinue if signs of hypersensitivity appear.
  • Use under medical supervision: only administer as directed by a qualified prescriber.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze.

Avoid Interactions

Leucovorin Teva may interact with several medications, requiring careful management.

Major Interactions (Avoid)

  • Methotrexate: concurrent use without proper timing can diminish methotrexate's anticancer effect.
  • Pemetrexed: may reduce efficacy of this antifolate if given together.
  • Trimethoprim: can increase risk of folate deficiency when combined.

Moderate Interactions (Monitor Closely)

  • NSAIDs: may affect renal clearance of calcium folinate.
  • Phenytoin: can accelerate folate metabolism, lowering therapeutic levels.
  • Oral contraceptives: may decrease folate availability, requiring monitoring.

Frequently Asked Questions

Leucovorin Teva, containing calcium folinate, is used to rescue patients from methotrexate toxicity, act as an adjunct in certain cancer chemotherapy protocols, and treat folate deficiency conditions. It provides a reduced form of folic acid that helps restore normal cellular function when folate pathways are disrupted.

Calcium folinate supplies a reduced folate that bypasses the dihydrofolate reductase block caused by drugs like methotrexate. By entering the folate cycle downstream, it replenishes tetrahydrofolate pools, allowing normal synthesis of nucleotides and DNA replication in healthy cells while preserving the antimetabolite effect on cancer cells.

The dose of Leucovorin Teva is individualized and determined by the prescribing clinician based on the specific indication, patient weight, renal function, and concurrent therapies. Healthcare professionals calculate the appropriate amount and schedule for each patient.

Safety data for calcium folinate during 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 healthcare provider after careful assessment.

To place an 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.

Leucovorin Teva provides a reduced, active form of folate that can bypass enzyme inhibition, unlike standard folic acid which requires conversion. This makes it especially effective for rescuing methotrexate toxicity and supporting chemotherapy, whereas regular folate supplements are primarily used for dietary deficiency without the same rescue capability.

Leucovorin Teva should be stored at 2‑8 °C, protected from light, and kept in its original packaging. It must not be frozen or shaken vigorously. If the product reaches room temperature, it should be used promptly and not re‑refrigerated.

Leucovorin Teva is administered by a qualified healthcare professional via epidural, intrabursal, or intracoronary injection, depending on the clinical indication. The route, dosage, and infusion rate are determined by the prescriber and follow institutional protocols.

Serious risks include anaphylactic reactions, severe skin disorders such as Stevens‑Johnson syndrome, hemolytic anemia (especially in G6PD‑deficient patients), acute renal failure, and thromboembolic events. Patients should be monitored closely for any signs of these conditions during therapy.

Leucovorin Teva is contraindicated in patients with known hypersensitivity to calcium folinate or any excipients in the formulation. Caution is also advised for individuals with severe renal or hepatic impairment, G6PD deficiency, or those receiving conflicting antifolate agents without proper timing.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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