Product image of Micafungina Teva (Micafungin) supplied by GNH India

Micafungina Teva

Active Ingredient:
Micafungin
Origin:
EU

Micafungina Teva (Micafungin)

Micafungin, the active ingredient in Micafungina Teva, is an echinocandin presented as an intravenous formulation for hospital use. It is employed to treat serious fungal infections such as invasive candidiasis, Candida esophagitis, peritonitis, and febrile neutropenia in immunocompromised patients. It is indicated for patients with systemic fungal infections who require intravenous therapy and is administered under medical supervision.
GNH India supplies Micafungina Teva as a licensed, GDP‑compliant supplier serving hospitals, transplant and oncology centres, pharmacies and clinics worldwide, with regulated quality and temperature‑controlled logistics.

Manufacturer / TM Owner

Teva B.V

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Indications & Clinical Uses

Micafungin is an echinocandin antifungal used to treat invasive Candida infections and related conditions.

  • Invasive candidiasis: effective treatment of bloodstream and deep‑tissue Candida infections.
  • Candida esophagitis: eradicates Candida infection of the esophagus.
  • Candida peritonitis: resolves intra‑abdominal Candida infection.
  • Febrile neutropenia: used as empirical therapy for suspected fungal infection in neutropenic patients.

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 disrupting cell‑wall formation, the drug leads to osmotic instability and fungal cell lysis, providing fungicidal activity against susceptible Candida species.

Side Effects

Micafungin may cause a range of adverse reactions, most of which are manageable.

Common Side Effects

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

Serious or Rare Side Effects

  • Severe hepatic dysfunction: jaundice or hepatic failure.
  • Anaphylaxis: acute hypersensitivity with respiratory compromise.
  • Renal impairment: acute kidney injury or worsening renal function.
  • Hematologic abnormalities: severe neutropenia or thrombocytopenia.
  • Severe skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.

Precautions & Warnings

Before initiating Micafungin therapy, clinicians should assess patient-specific risk factors and monitor relevant parameters.

  • Renal function: monitor serum creatinine in patients with pre‑existing renal impairment.
  • Hepatic function: check liver enzymes before and during treatment.
  • Hypersensitivity: discontinue immediately if severe allergic reaction occurs.
  • Concomitant antifungals: evaluate potential additive toxicity when used with other antifungal agents.
  • Pregnancy and lactation: use only if the potential benefit justifies the potential risk to the fetus or infant.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Micafungin can interact with several drug classes; awareness helps prevent adverse outcomes.

Major Interactions (Avoid)

  • Strong CYP3A4 inducers (e.g., rifampin) may markedly reduce micafungin exposure.
  • Co‑administration with other echinocandins can increase toxicity without added benefit.
  • Concurrent use with azoles that share metabolic pathways may lead to unpredictable plasma levels.

Moderate Interactions (Monitor Closely)

  • Immunosuppressants such as cyclosporine may require dose adjustment.
  • Warfarin therapy may be affected; monitor INR closely.
  • Nephrotoxic agents (e.g., aminoglycosides) warrant renal function monitoring.
  • Concomitant use with drugs that prolong QT interval should be evaluated.
  • Adjust dosing when combined with agents that alter protein binding.

Frequently Asked Questions

Micafungina Teva, containing micafungin, is indicated for the treatment of invasive candidiasis, Candida esophagitis, Candida peritonitis, and for empirical therapy of febrile neutropenia when a fungal infection is suspected. These uses reflect its activity against a broad range of Candida species.

Micafungin inhibits the fungal enzyme β‑(1,3)‑D‑glucan synthase, which is essential for constructing β‑(1,3)‑D‑glucan, a key structural polysaccharide of the fungal cell wall. By blocking this pathway, the drug weakens the cell wall, leading to osmotic instability and cell death.

The dosage of Micafungina Teva is determined by the prescribing clinician based on the specific infection, patient weight, renal and hepatic function, and other clinical factors. The product is supplied as an intravenous preparation and should be administered under medical supervision.

The safety of micafungin in pregnancy and lactation has not been definitively established. It 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 a qualified healthcare professional.

To request Micafungina Teva, 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 handling if needed), and import documentation.

Micafungina 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 strains.

Micafungina Teva should be stored at 2‑8 °C (refrigerated). Keep the vial in its original packaging, protect it from light, and avoid freezing or shaking the solution. Once reconstituted, follow the manufacturer’s guidance for stability and use within the recommended time frame.

Micafungina Teva is administered intravenously by slow infusion, typically over 30‑60 minutes, under the supervision of qualified healthcare personnel. The exact infusion rate and duration are determined by the prescriber based on the patient’s condition and institutional protocols.

Serious adverse events include severe hepatic dysfunction, anaphylactic reactions, acute renal impairment, and rare but life‑threatening skin reactions such as Stevens‑Johnson syndrome. Patients should be monitored closely for signs of liver injury, hypersensitivity, and renal function changes throughout therapy.

Micafungina Teva is contraindicated in patients with a known hypersensitivity to micafungin or any component of the formulation. Caution is also advised for individuals with severe hepatic or renal impairment, and it should be avoided in pregnant or breastfeeding women unless the clinical benefit justifies potential risks.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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