Product image of Micafungina Reig Jofre (Micafungin Sodium) supplied by GNH India

Micafungina Reig Jofre

Active Ingredient:
Micafungin Sodium
Origin:
EU

Micafungina Reig Jofre (Micafungin Sodium)

Micafungin Sodium, the active ingredient in Micafungina Reig Jofre, is an echinocandin presented as an intravenous solution for IV use. It is employed to treat invasive candidiasis, esophageal candidiasis, Candida auris infections, and to provide prophylaxis in hematopoietic stem‑cell transplantation.

GNH India supplies Micafungina Reig Jofre as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides reliable cold‑chain logistics for this parenteral product across global markets.

Manufacturer / TM Owner

Laboratorio Reig Jofre, S.A.

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Indications & Clinical Uses

Micafungin Sodium is an echinocandin antifungal that inhibits fungal cell wall synthesis, making it effective for several serious Candida infections.

  • Invasive candidiasis: rapid clearance of bloodstream infection and reduction of mortality in adult and pediatric patients.
  • Esophageal candidiasis: promotes healing of mucosal lesions and alleviates dysphagia.
  • Candida auris infections: provides effective treatment against this multidrug‑resistant yeast.
  • Prophylaxis in hematopoietic stem‑cell transplantation: prevents invasive fungal disease during the neutropenic phase.

How It Works

  • Micafungin Sodium selectively inhibits the enzyme β‑1,3‑D‑glucan synthase, which is essential for synthesis of β‑1,3‑D‑glucan, a critical component of the fungal cell wall. By blocking this pathway, the drug weakens the cell wall, leading to osmotic instability and fungal cell death, while having minimal effect on human cells that lack this enzyme.

Side Effects

Micafungin Sodium may be associated with a range of adverse reactions, which are categorized by frequency and severity.

Common Side Effects

  • Infusion‑related reactions: flushing, chills, or mild hypotension during administration.
  • Gastrointestinal discomfort: nausea, vomiting, or abdominal pain.
  • Elevated liver enzymes: transient increases in ALT or AST.

Serious or Rare Side Effects

  • Severe hepatic injury: jaundice or hepatic failure requiring monitoring.
  • Anaphylaxis: acute allergic reaction with respiratory distress.
  • Stevens‑Johnson syndrome or toxic epidermal necrolysis: severe skin blistering and detachment.

Precautions & Warnings

Prior to initiating Micafungin Sodium therapy, clinicians should consider several safety precautions to minimize risk.

  • Monitor liver function: obtain baseline and periodic ALT/AST levels during treatment.
  • Assess renal function: evaluate serum creatinine and adjust therapy if significant impairment occurs.
  • Check for hypersensitivity: discontinue immediately if signs of rash, angioedema, or anaphylaxis develop.
  • Use caution with concomitant nephrotoxic agents: increase monitoring for additive renal toxicity.
  • Adjust dose in severe hepatic impairment: consider reduced dosing or alternative therapy when indicated.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Micafungin Sodium can interact with other medicines, requiring attention to avoid reduced efficacy or increased toxicity.

Major Interactions (Avoid)

  • Cyclosporine: micafungin may increase cyclosporine blood concentrations, risking nephrotoxicity.
  • Tacrolimus: co‑administration can raise tacrolimus levels, necessitating dose reduction.
  • Rifampin: strong enzyme induction may lower micafungin exposure, compromising antifungal activity.

Moderate Interactions (Monitor Closely)

  • Azole antifungals (e.g., fluconazole): may increase micafungin levels, requiring therapeutic monitoring.
  • Warfarin: potential alteration of INR, monitor coagulation parameters.
  • Statins (e.g., simvastatin): possible increased risk of myopathy, observe muscle symptoms.
  • Oral contraceptives: micafungin may reduce hormonal efficacy, advise alternative contraception.

Frequently Asked Questions

Micafungina Reig Jofre contains micafungin sodium, an echinocandin antifungal indicated for the treatment of invasive candidiasis, esophageal candidiasis, infections caused by Candida auris, and for prophylaxis of fungal disease in patients undergoing hematopoietic stem‑cell transplantation.

Micafungin sodium inhibits the fungal enzyme β‑1,3‑D‑glucan synthase, which is required for the synthesis of β‑1,3‑D‑glucan, a key structural component of the fungal cell wall. Blocking this enzyme weakens the wall, leading to osmotic instability and fungal cell death while sparing human cells.

The dose of Micafungina Reig Jofre is determined by the prescribing clinician based on the specific indication, patient weight, renal and hepatic function, and other clinical factors. No fixed dosing regimen is provided here; the prescriber sets the appropriate regimen.

Safety data for micafungin sodium in pregnancy and lactation are limited, and the product carries an unknown pregnancy category. It should be used only if the potential benefit justifies the potential risk to the fetus or infant, and decisions should be made in consultation with a healthcare professional.

To place an order, submit an enquiry on the Micafungina Reig Jofre 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 any required import documentation.

Micafungin belongs to the echinocandin class, which targets the fungal cell wall, whereas azoles inhibit ergosterol synthesis and polyenes bind directly to ergosterol. Echinocandins, including micafungin, are often preferred for invasive Candida infections because of their rapid fungicidal activity and lower drug‑drug interaction potential compared with many azoles.

The product must be stored refrigerated at 2‑8 °C, protected from light, and must not be frozen or shaken. It should be kept in its original packaging until use to maintain stability and potency.

Micafungina Reig Jofre is administered intravenously by a qualified healthcare professional. The solution is typically diluted in a compatible IV fluid and infused over about one hour, following the dosing instructions provided by the prescriber.

Serious adverse events include severe hepatic injury (jaundice or liver failure), anaphylactic reactions, and severe cutaneous reactions such as Stevens‑Johnson syndrome or toxic epidermal necrolysis. Patients should be monitored closely for signs of liver dysfunction, allergic response, or skin changes during therapy.

Micafungina Reig Jofre should be avoided in individuals with known hypersensitivity to micafungin or any component of the formulation. Caution is also advised for patients with severe hepatic impairment, as safety has not been established in this population.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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