GNH USA

Europe — EMA

Iruxol Mono

GNH USA supplies Iruxol Mono (Collagenase Clostridium Histolyticum), a proteolytic enzyme for debridement of necrotic tissue in chronic wounds.

Collagenase Clostridium Histolyticum, Protease

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What is Collagenase Clostridium Histolyticum, Protease?

Collagenase Clostridium Histolyticum, the active ingredient in Iruxol Mono, is a proteolytic enzyme presented as a topical preparation for topical use. It facilitates enzymatic debridement of necrotic tissue in chronic and dermatologic wounds, helping to promote healthy tissue regeneration in patients with difficult‑to‑heal lesions.

GNH USA supplies Iruxol Mono as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

What is Collagenase Clostridium Histolyticum, Protease used for?

Iruxol Mono is a proteolytic enzyme indicated for debridement in wound‑care and dermatology. It assists clinicians in removing non‑viable tissue to support healing.

- Chronic wounds: promotes removal of necrotic tissue to accelerate wound closure. - Pressure ulcers: enzymatically debrides dead tissue, facilitating recovery. - Diabetic foot ulcers: assists in clearing devitalized tissue, improving the wound environment.

What are the side effects of Collagenase Clostridium Histolyticum, Protease?

Topical application of Iruxol Mono may be associated with local reactions.

Common Side Effects: - Redness at application site: mild irritation. - Swelling: localized edema. - Itching: transient pruritus. - Burning sensation: brief discomfort. - Dryness: mild skin desiccation. - Minor bleeding: slight oozing from debrided area.

Serious or Rare Side Effects: - Severe allergic reaction: hives, swelling of face or throat. - Extensive tissue damage: excessive enzymatic activity. - Infection: secondary bacterial colonisation. - Persistent ulceration: failure to heal. - Systemic hypersensitivity: fever, malaise. - Necrotizing fasciitis: rapidly spreading tissue necrosis.

What precautions apply to Collagenase Clostridium Histolyticum, Protease?

When using Iruxol Mono, clinicians should observe several safety measures.

- Assess wound: confirm presence of necrotic tissue before application. - Avoid healthy tissue: limit exposure to viable skin to prevent unnecessary degradation. - Monitor for infection: watch for signs of bacterial overgrowth. - Contraindications: do not use on patients with known hypersensitivity to collagenase or protease enzymes. - Pediatric use: exercise caution, as safety data are limited. - Store below 25°C: keep in the original container, protect from moisture and light.

What does Collagenase Clostridium Histolyticum, Protease interact with?

Iruxol Mono may interact with other topical agents or systemic medications.

Major Interactions (Avoid): - Concurrent use of other proteolytic enzymes: may increase tissue breakdown. - Topical corticosteroids: can reduce enzyme efficacy. - Anticoagulants applied locally: heightened risk of bleeding.

Moderate Interactions (Monitor Closely): - Systemic antibiotics: monitor for altered wound flora. - Immunosuppressants: may affect healing response. - Moisturizers containing occlusive agents: could impede enzyme activity.

Frequently asked questions

What is Iruxol Mono used for?+
Iruxol Mono is a prescription topical formulation that contains collagenase clostridium histolyticum. It is used by healthcare professionals to enzymatically debride necrotic tissue in chronic wounds such as pressure ulcers, diabetic foot ulcers, and other dermatologic lesions, helping to prepare the wound bed for healing.
How does collagenase clostridium histolyticum work in Iruxol Mono?+
The collagenase enzyme selectively breaks down collagen and other extracellular matrix proteins that constitute dead or devitalized tissue. By hydrolyzing these structural proteins, the product softens and removes necrotic material without harming viable tissue, thereby facilitating a cleaner wound environment for regeneration.
What is the usual dose of Iruxol Mono?+
The dosage and frequency of Iruxol Mono are determined by the prescribing clinician based on wound size, depth, and patient condition. The prescriber will specify the amount of product to apply, the interval between applications, and the total duration of therapy.
Is Iruxol Mono safe to use during pregnancy or breastfeeding?+
Safety data for Iruxol Mono in pregnancy and lactation are limited. It should only be used if the potential benefit to the mother outweighs any possible risk to the fetus or infant, and this decision must be made by a qualified healthcare professional.
How do I order Iruxol Mono from GNH USA?+
To request Iruxol Mono, submit an enquiry on the product page at gnh-usa.com, indicating the required quantity. GNH USA works with hospitals, pharmacies, and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including any cold‑chain requirements), and necessary import documentation.
How does Iruxol Mono compare with other wound‑debridement agents?+
Iruxol Mono’s collagenase enzyme offers selective enzymatic debridement, which can be gentler than mechanical or surgical methods and may preserve more healthy tissue compared with non‑specific proteolytic creams. It is often preferred when precise removal of necrotic tissue is required, whereas other agents may act more broadly or cause greater irritation.
What are the storage and handling requirements for Iruxol Mono?+
Iruxol Mono should be stored below 25 °C in its original packaging, protected from moisture and direct light. Keep the container tightly closed when not in use and avoid exposing the product to extreme temperatures to maintain enzyme stability.
How is Iruxol Mono applied?+
The product is applied topically to the cleaned wound surface using a sterile applicator or gloved finger, as directed by the prescriber. The recommended amount is spread evenly over the necrotic area, and the wound is then covered with an appropriate dressing if required.
What are the most serious risks associated with Iruxol Mono?+
Serious risks include severe allergic reactions such as anaphylaxis, extensive tissue damage from over‑debridement, secondary infections, and rare cases of necrotizing fasciitis. Patients should be monitored closely for signs of hypersensitivity, worsening ulceration, or systemic infection.
Who should not use Iruxol Mono?+
Iruxol Mono should not be used in individuals with a known hypersensitivity to collagenase, protease enzymes, or any excipients in the formulation. It is also contraindicated on healthy, non‑necrotic skin and should be avoided in patients where the risk of excessive tissue breakdown outweighs potential benefits.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Collagenase Clostridium Histolyticum, Protease
Route
Cutaneous Use
Manufacturer
Smith & Nephew Gmbh
Origin
EU

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