Product image of Kalciumfolinat Stada (Calcium Folinate) supplied by GNH India

Kalciumfolinat Stada

Active Ingredient:
Calcium Folinate
Origin:
EU

Kalciumfolinat Stada (Calcium Folinate)

Calcium folinate, the active ingredient in Kalciumfolinat Stada, is a folate analog presented as an injectable solution for intramuscular and intravenous use. It is employed to counteract methotrexate toxicity, prevent folate deficiency, and support patients receiving folate‑dependent chemotherapy regimens.

GNH India supplies Kalciumfolinat Stada as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres and pharmacies worldwide. The company adheres to EU quality standards and provides reliable global distribution.

Manufacturer / TM Owner

Stada Arzneimittel Ag

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Indications & Clinical Uses

Calcium folinate is used in clinical situations that involve folate pathway disruption or increased folate demand.

  • Methotrexate toxicity: provides rescue therapy that rapidly restores folate pools and reduces toxic effects.
  • Folate deficiency: prevents or treats low folate levels in patients at risk.
  • Cancer chemotherapy protocols: serves as an adjunct to lessen folate‑antagonist toxicity during treatment.

How It Works

  • Calcium folinate is a reduced form of folic acid that bypasses the dihydrofolate reductase step. By directly supplying 5‑methyltetrahydrofolate, it restores intracellular folate‑dependent one‑carbon transfer reactions, DNA synthesis, and methylation processes that are inhibited by antifolate drugs such as methotrexate. This biochemical bypass re‑establishes normal cellular function without requiring enzymatic reduction.

Side Effects

Calcium folinate may be associated with several adverse reactions, ranging from mild to severe.

Common Side Effects

  • Nausea: mild to moderate gastrointestinal upset.
  • Vomiting: occasional emesis following injection.
  • Injection site pain: local discomfort or erythema.
  • Headache: transient cranial discomfort.
  • Fatigue: generalized tiredness.
  • Mild fever: low‑grade temperature elevation.

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction requiring immediate medical attention.
  • Severe hypotension: marked drop in blood pressure post‑administration.
  • Renal toxicity: impaired kidney function, especially with high doses.
  • Hepatic dysfunction: elevated liver enzymes or hepatitis.
  • Severe neutropenia: marked reduction in neutrophil count.
  • Thrombocytopenia: significant drop in platelet levels.

Precautions & Warnings

When using calcium folinate, several precautionary measures should be observed to ensure safe administration.

  • Renal impairment: adjust dose and monitor renal function closely.
  • Hepatic dysfunction: evaluate liver enzymes before and during therapy.
  • Pregnancy: potential risk to the fetus; use only if benefits outweigh risks.
  • Concomitant methotrexate: monitor folate levels and clinical response.
  • Pediatric use: exercise caution and adjust dosing based on weight and age.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Calcium folinate can interact with several medicines, altering efficacy or safety.

Major Interactions (Avoid)

  • Methotrexate: may reduce antidotal effect if not timed correctly.
  • Antifolate agents (e.g., pemetrexed): antagonize therapeutic action.
  • Trimethoprim: potentiates folate deficiency.
  • Phenytoin: may decrease folate levels.
  • Carbamazepine: induces folate metabolism, reducing effectiveness.

Moderate Interactions (Monitor Closely)

  • NSAIDs: may increase risk of renal toxicity.
  • Oral contraceptives: folate supplementation can affect hormone metabolism.
  • Warfarin: folate may alter anticoagulant response.
  • Sulfonamides: combined effect on folate pathways.
  • Allopurinol: potential for enhanced toxicity in renal patients.

Frequently Asked Questions

Kalciumfolinat Stada contains calcium folinate, which is used as an antidote for methotrexate toxicity, to prevent or treat folate deficiency, and as an adjunct in cancer chemotherapy protocols to reduce folate‑antagonist side effects.

Calcium folinate provides a reduced form of folic acid that bypasses the dihydrofolate reductase step, directly supplying 5‑methyltetrahydrofolate. This restores folate‑dependent cellular processes such as DNA synthesis and methylation that are blocked by antifolate drugs.

The dose of calcium folinate is individualized. A qualified prescriber determines the appropriate amount based on the patient’s clinical condition, the severity of methotrexate exposure, renal and hepatic function, and other relevant factors.

Safety in pregnancy and lactation has not been fully established. It should be used only if the potential benefit justifies the possible risk to the fetus or infant, and the decision must be made by the treating physician.

To place an order, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies 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.

Kalciumfolinat Stada is a form of calcium folinate (folinic acid), which is a reduced folate that bypasses dihydrofolate reductase inhibition. Compared with folic acid, it acts more rapidly in rescue situations and is the preferred antidote for methotrexate toxicity.

The product must be stored at 2‑8 °C, kept refrigerated, protected from light, and must not be frozen or shaken. Follow the manufacturer’s packaging instructions to maintain product stability.

Kalciumfolinat Stada is supplied for intramuscular or intravenous injection. Administration is performed by a qualified healthcare professional, who selects the appropriate route, volume, and infusion rate according to the prescribing information.

Serious risks include anaphylactic reactions, severe hypotension, renal toxicity, hepatic dysfunction, severe neutropenia, and thrombocytopenia. Patients should be monitored for these events, especially when high doses are used or when co‑administered with nephrotoxic or hepatotoxic agents.

Patients with known hypersensitivity to calcium folinate or any excipients should avoid the product. Caution is also advised in individuals with severe renal or hepatic impairment, and it should not be used in pregnancy unless clearly indicated by a physician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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