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

Micafungin Teva

Active Ingredient:
Micafungin
Origin:
EU

Micafungin Teva (Micafungin)

Micafungin, the active ingredient in Micafungin Teva, is an echinocandin presented as an intravenous solution for intravenous use. It treats invasive candidiasis, esophageal candidiasis, and is used for prophylaxis of Candida infections in patients undergoing hematopoietic stem cell transplantation.

GNH India supplies Micafungin Teva as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres and pharmacies worldwide. The company adheres to stringent quality standards and provides reliable logistics for global distribution. Clients benefit from dedicated regulatory support and consistent product availability across regions.

Manufacturer / TM Owner

Teva B.V

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Indications & Clinical Uses

  • Micafungin is an echinocandin antifungal indicated for the following clinical situations:
  • Invasive candidiasis: provides effective treatment of bloodstream and deep‑tissue Candida infections, reducing mortality in adult and pediatric patients.
  • Esophageal candidiasis: eradicates Candida infection of the esophagus in immunocompromised patients, improving swallowing function and nutritional intake.
  • Prophylaxis in hematopoietic stem cell transplantation: prevents Candida infections during the neutropenic phase, supporting engraftment and reducing infection‑related complications.

How It Works

  • Micafungin 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 disrupting cell‑wall construction, the drug leads to osmotic instability and cell lysis, selectively targeting fungi while sparing human cells. The inhibition is concentration‑dependent and does not affect mammalian glucan pathways, resulting in a favorable safety profile. Micafungin is administered intravenously, allowing rapid achievement of therapeutic plasma concentrations.

Side Effects

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

Common Side Effects

  • Elevated liver enzymes (ALT, AST): mild to moderate increases observed.
  • Fever: transient temperature rise during therapy.
  • Nausea: occasional gastrointestinal discomfort.
  • Headache: mild headache reported in some patients.

Serious or Rare Side Effects

  • Hypersensitivity reactions: rash, pruritus, or anaphylaxis may occur.
  • Severe hepatic dysfunction: marked elevation of transaminases or bilirubin.
  • Renal impairment: rare cases of increased serum creatinine.

Precautions & Warnings

When using Micafungin, clinicians should consider several precautionary measures to ensure safe administration.

  • Renal function: assess baseline renal status; dose adjustment may be required in severe impairment.
  • Hepatic function: monitor liver enzymes during treatment, especially in patients with pre‑existing liver disease.
  • Drug interactions: review concomitant medications for potential major or moderate interactions.
  • Pregnancy and lactation: use only if potential benefit justifies potential risk; data are limited.
  • Infusion reactions: monitor for signs of fever, chills, or hypotension during IV administration.
  • 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)

  • Rifampin: strong enzyme inducer that may markedly reduce micafungin plasma concentrations.
  • Strong CYP3A4 inducers (e.g., carbamazepine, phenytoin): may decrease exposure and compromise efficacy.
  • Concurrent use with other echinocandins: increased risk of additive toxicity.

Moderate Interactions (Monitor Closely)

  • Azole antifungals (e.g., fluconazole, voriconazole): may increase micafungin levels; monitor for toxicity.
  • Immunosuppressants (e.g., tacrolimus, cyclosporine): possible altered concentrations; adjust dosing as needed.
  • Warfarin: may enhance anticoagulant effect; monitor INR.

Frequently Asked Questions

Micafungin Teva is indicated for the treatment of invasive candidiasis, including bloodstream and deep‑tissue infections, for esophageal candidiasis in immunocompromised patients, and for prophylaxis of Candida infections in individuals undergoing hematopoietic stem cell transplantation during the neutropenic phase.

Micafungin blocks the 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 lysis, which selectively kills fungal cells while sparing human tissues.

The dose of Micafungin Teva is determined by the prescribing clinician based on the specific indication, patient weight, renal and hepatic function, and the severity of the infection. No fixed regimen is provided here; the prescriber tailors the regimen to each individual case.

Safety data for micafungin in pregnancy and lactation are limited. It should be used only if the potential therapeutic benefit justifies any potential risk to the fetus or infant, and the decision should be made by the treating physician in consultation with the patient.

To order Micafungin Teva, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, and will request trade or institutional credentials before providing pricing, availability, shipping details (including cold‑chain where required) and import documentation.

Micafungin belongs to the echinocandin class, which targets the fungal cell wall, whereas azoles inhibit ergosterol synthesis in the cell membrane. Echinocandins like micafungin are generally fungicidal against Candida species and have a lower risk of drug‑drug interactions, but they are administered intravenously, unlike many oral azoles.

Micafungin Teva should be stored at 2‑8 °C (refrigerated). Keep the product in its original packaging, protect it from light, and do not freeze or shake the vial. Maintaining the cold‑chain ensures stability and potency of the intravenous solution.

Micafungin is given by intravenous infusion. The prescriber determines the infusion rate and duration, which typically ranges from 30 to 60 minutes. The solution is diluted in compatible IV fluid and administered through a peripheral or central line under aseptic conditions.

The most serious risks include hypersensitivity reactions that can progress to anaphylaxis, severe hepatic dysfunction manifested by marked elevations in transaminases or bilirubin, and rare cases of renal impairment. Patients should be monitored closely for signs of these events throughout treatment.

Micafungin is contraindicated in individuals with a known hypersensitivity to micafungin or any component of the formulation. Caution is also advised for patients with severe hepatic impairment, and the drug should be used only after careful risk‑benefit assessment in such cases.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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