Product image of Levofolic (Levoleucovorin Disodium) supplied by GNH India

Levofolic

Active Ingredient:
Levoleucovorin Disodium
Origin:
EU

Levofolic (Levoleucovorin Disodium)

Levoleucovorin disodium, the active ingredient in Levofolic, is a folate analog presented as an intravenous solution for IV use. It restores reduced folate pools, helping to mitigate the effects of antifolate drugs and to correct folate deficiency in patients undergoing chemotherapy or with impaired folate metabolism.

GNH India supplies Levofolic as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide, meeting stringent EU quality standards and is recognized for reliable on‑time delivery across multiple continents.

Manufacturer / TM Owner

Medac Gesellschaft Für Klinische Spezialpräparate Mbh (Wedel)

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Indications & Clinical Uses

Levofolic provides reduced folate to support patients receiving antifolate chemotherapy or with folate deficiency.

  • Methotrexate toxicity: restores folate metabolism to reduce mucosal and hematologic toxicity.
  • Pemetrexed therapy: mitigates folate‑related side effects during treatment.
  • Folate deficiency: supplies active folate to correct deficiency in patients unable to absorb folic acid.
  • High‑dose chemotherapy support: enhances folate‑dependent DNA synthesis in normal cells during intensive regimens.

How It Works

  • Levoleucovorin disodium is a reduced form of folate that bypasses the dihydrofolate reductase step, directly entering the folate cycle. By supplying 5‑methyltetrahydrofolate equivalents, it restores one‑carbon transfer reactions essential for nucleotide synthesis and methylation, thereby supporting DNA replication and repair in normal cells while counteracting the effects of antifolate agents.

Side Effects

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

Common Side Effects

  • Nausea: mild to moderate upset stomach.
  • Vomiting: occasional emesis following infusion.
  • Fever or chills: transient temperature rise.
  • Headache: mild discomfort during or after administration.
  • Injection site reactions: erythema, pain, or swelling at the IV site.
  • Elevated liver enzymes: mild, transient increase.

Serious or Rare Side Effects

  • Anaphylactic reaction: sudden severe allergy requiring emergency care.
  • Acute renal failure: rapid decline in kidney function.
  • Severe hypotension: marked drop in blood pressure during infusion.
  • Pulmonary edema: fluid accumulation in lungs.
  • Cardiac arrhythmias: irregular heart rhythms.
  • Severe electrolyte disturbances: dangerous shifts in potassium, calcium, or magnesium.

Precautions & Warnings

Levofolic should be used with careful clinical monitoring.

  • Renal function assessment: evaluate creatinine clearance before and during therapy.
  • Hematologic monitoring: check complete blood counts regularly.
  • Hypersensitivity screening: avoid use in patients with known allergy to folate derivatives.
  • Concomitant nephrotoxic drugs: use caution when combined with agents such as aminoglycosides.
  • Hepatic impairment: adjust dosing or monitor liver enzymes closely.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Levofolic may interact with several drug classes; awareness of interaction severity guides management.

Major Interactions (Avoid)

  • Methotrexate: timing must be coordinated to prevent excessive toxicity.
  • Pemetrexed: concurrent use requires precise scheduling to avoid reduced efficacy.
  • High‑dose cytarabine: may increase risk of myelosuppression.

Moderate Interactions (Monitor Closely)

  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): can affect renal clearance of folate.
  • Aminoglycoside antibiotics: combined nephrotoxic potential.
  • Loop diuretics: may exacerbate electrolyte imbalances when used together.

Frequently Asked Questions

Levofolic is an intravenous formulation of levoleucovorin disodium that provides a reduced form of folate. It is used to rescue patients from the toxic effects of antifolate chemotherapy such as methotrexate, to lessen side effects of pemetrexed, and to correct folate deficiency when oral folic acid is ineffective.

Levoleucovorin disodium bypasses the dihydrofolate reductase step, directly supplying active folate metabolites. This restores one‑carbon transfer pathways needed for DNA synthesis and methylation, allowing normal cells to recover from antifolate‑induced blockade while supporting cellular metabolism.

The dose of Levofolic is determined by the prescribing clinician based on the specific indication, patient weight, renal function, and the concomitant chemotherapy regimen. Only a qualified health‑care professional should set the dosage and infusion schedule.

The safety of Levofolic in pregnancy and lactation has not been fully established. It should only be used if the potential benefit justifies any potential risk to the fetus or infant, and the decision must be made by a qualified health‑care provider.

To order Levofolic, 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.

Levofolic (levoleucovorin disodium) is chemically equivalent to other folinic acid preparations but is supplied as a sterile IV solution meeting EU GMP standards. Compared with oral folic acid, it provides immediate bioavailability and bypasses intestinal absorption issues, making it preferred for rapid rescue in high‑risk chemotherapy settings.

Levofolic must be stored refrigerated at 2‑8 °C, protected from light, and should never be frozen or shaken. Before use, inspect the vial for particulate matter or discoloration and allow it to reach room temperature if required by the administration protocol.

Levofolic is administered intravenously by a qualified health‑care professional. The infusion rate and volume are set according to the prescribing information and the patient’s clinical condition, typically over a period of several minutes to an hour.

Serious risks include anaphylactic reactions, acute renal failure, severe hypotension, pulmonary edema, cardiac arrhythmias, and significant electrolyte disturbances. Prompt recognition and management of these events are essential, and patients should be monitored closely during and after infusion.

Levofolic should be avoided in patients with known hypersensitivity to levoleucovorin or any component of the formulation. Caution is also advised for individuals with severe renal or hepatic impairment, uncontrolled cardiovascular disease, or those receiving incompatible medications without proper monitoring.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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