Product image of Micafungine Accord (Micafungin) supplied by GNH India

Micafungine Accord

Active Ingredient:
Micafungin
Origin:
EU

Micafungine Accord (Micafungin)

Micafungin, the active ingredient in Micafungine Accord, is an echinocandin presented as an intravenous formulation for hospital use. It treats serious fungal infections such as invasive candidiasis, Candida esophagitis, peritonitis and bloodstream infections in immunocompromised patients. It is effective against most Candida species, including those resistant to azole therapy.

GNH India supplies Micafungine Accord as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide, ensuring quality‑assured products and reliable logistics across global markets.

Manufacturer / TM Owner

Accord Healthcare B.V.

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Indications & Clinical Uses

Micafungin is used to treat invasive fungal infections caused by Candida species.

  • Invasive candidiasis: eradicates bloodstream and deep‑tissue Candida infections.
  • Candida esophagitis: resolves esophageal lesions and associated symptoms.
  • Candida peritonitis: clears intra‑abdominal Candida infection.
  • Candida bloodstream infections: eliminates fungemia and prevents dissemination.

How It Works

  • Micafungin inhibits the enzyme β‑(1,3)‑D‑glucan synthase, which is essential for synthesizing β‑(1,3)‑D‑glucan, a critical component of the fungal cell wall. By blocking this pathway, the drug weakens the cell wall integrity, leading to osmotic instability and fungal cell death, while having minimal effect on human cells that lack this target. The selective inhibition results in fungicidal activity against most Candida spp. and provides a broad spectrum of activity for severe systemic infections.

Side Effects

Micafungin may be associated with a range of adverse reactions, varying from mild to severe.

Common Side Effects

  • Fever: transient temperature rise during or after infusion.
  • Nausea: mild to moderate upset stomach.
  • Headache: occasional mild headache.
  • Infusion‑related reactions: flushing, chills, or rigors during administration.
  • Elevated liver enzymes: transient increase in ALT/AST.
  • Rash: mild skin erythema or pruritus.

Serious or Rare Side Effects

  • Hepatic failure: severe liver dysfunction requiring monitoring.
  • Severe allergic reactions: anaphylaxis with respiratory distress or shock.
  • Acute renal impairment: sudden rise in serum creatinine.
  • Severe hypotension: marked drop in blood pressure during infusion.
  • Stevens‑Johnson syndrome or toxic epidermal necrolysis: serious skin blistering.
  • Cardiovascular events: arrhythmias or myocardial infarction.

Precautions & Warnings

When using Micafungin, clinicians should observe specific safety measures to minimize risks.

  • Renal function: monitor serum creatinine and urine output.
  • Hepatic function: assess liver enzymes before and during therapy.
  • Concomitant antifungals: avoid overlapping use with other echinocandins.
  • Pregnancy and lactation: prescribe only if potential benefit outweighs risk.
  • Drug interactions: review patient’s medication list for CYP inducers or anticoagulants.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Micafungin can interact with other medicines, affecting its efficacy or safety.

Major Interactions (Avoid)

  • Strong CYP3A4 inducers (e.g., rifampin): may reduce micafungin exposure.
  • Co‑administration with other echinocandins: increased risk of toxicity.
  • High‑dose azoles (e.g., voriconazole): potential additive hepatotoxicity.

Moderate Interactions (Monitor Closely)

  • Azole antifungals (fluconazole, itraconazole): may increase liver enzyme levels.
  • Immunosuppressants (cyclosporine, tacrolimus): monitor blood concentrations.
  • Anticoagulants (warfarin): watch for altered INR values.

Frequently Asked Questions

Micafungine Accord contains micafungin, an echinocandin antifungal indicated for the treatment of serious Candida infections such as invasive candidiasis, Candida esophagitis, peritonitis and bloodstream infections in patients who require intravenous therapy.

Micafungin blocks the fungal enzyme β‑(1,3)‑D‑glucan synthase, preventing the synthesis of β‑(1,3)‑D‑glucan, an essential component of the fungal cell wall. This disruption weakens the wall, leading to osmotic instability and cell death while sparing human cells that lack this pathway.

The dosing regimen for Micafungine Accord is determined by the prescribing clinician based on the type and severity of the infection, patient weight, renal and hepatic function, and other clinical factors. No fixed dose is provided here.

Safety data for micafungin in pregnancy and lactation are limited. The product should be used only if the potential benefit to the mother outweighs any possible risk to the fetus or infant, and the decision should be made by the treating physician.

To place an order, submit an enquiry on the Micafungine Accord 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 where required) and import documentation.

Micafungine Accord belongs to the echinocandin class, which targets the fungal cell wall, whereas azoles inhibit ergosterol synthesis and polyenes bind directly to membrane sterols. Echinocandins like micafungin are generally well‑tolerated, have a low potential for drug‑drug interactions, and are effective against many azole‑resistant Candida species.

Micafungine Accord should be stored at 2‑8 °C (refrigerated). Keep the vial in its original packaging, protect it from light, and do not freeze or shake the solution. Follow standard aseptic techniques when preparing the intravenous infusion.

Micafungine Accord is supplied as an injectable solution for intravenous infusion. The infusion rate and duration are set by the prescribing clinician, typically administered over one to two hours, and may be repeated daily depending on the infection being treated.

Serious adverse events include hepatic failure, severe allergic reactions such as anaphylaxis, acute renal impairment, marked hypotension during infusion, and rare skin disorders like Stevens‑Johnson syndrome or toxic epidermal necrolysis. Prompt medical evaluation is required if any of these occur.

Patients with a known hypersensitivity to micafungin or any component of the formulation should avoid the product. Caution is also advised for individuals with severe liver dysfunction, uncontrolled renal failure, or those receiving concurrent therapy that may increase toxicity risk.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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