GNH USA

Europe — EMA

Ivacaftor Stada Nordic

GNH USA supplies Ivacaftor Stada Nordic (Ivacaftor), a CFTR potentiator for cystic fibrosis patients with gating mutations. Request a quote for global supply.

Ivacaftor

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What is Ivacaftor?

Ivacaftor, the active ingredient in Ivacaftor Stada Nordic, is a CFTR potentiator presented as an oral formulation for oral use. It is indicated for the treatment of cystic fibrosis in patients who carry specific gating mutations of the CFTR gene.

GNH USA supplies Ivacaftor Stada Nordic 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 regulatory‑approved products to meet global demand across diverse markets.

What is Ivacaftor used for?

Ivacaftor is a CFTR potentiator used in the management of cystic fibrosis caused by gating mutations.

- Cystic fibrosis with G551D mutation: Improves CFTR channel opening and respiratory outcomes. - Cystic fibrosis with other class III gating mutations: Enhances chloride transport and clinical parameters. - Cystic fibrosis in patients aged 12 years and older with at least one approved gating mutation: Increases lung function and reduces pulmonary exacerbations.

What are the side effects of Ivacaftor?

Common Side Effects: - Headache: mild to moderate intensity. - Diarrhea: usually transient. - Nausea: may occur after dosing. - Abdominal pain: occasional discomfort. - Upper respiratory tract infection: mild symptoms. - Rash: mild skin irritation.

Serious or Rare Side Effects: - Elevated liver enzymes: monitor hepatic function. - Cataracts: periodic eye examinations recommended. - Severe rash or hypersensitivity reactions: seek immediate medical attention. - Arrhythmia: rare cardiac rhythm disturbances. - Anaphylaxis: life‑threatening allergic reaction requiring emergency care.

What precautions apply to Ivacaftor?

Before initiating therapy, consider the following precautions: - Monitor liver function: baseline and periodic tests are recommended. - Assess for drug interactions: review all concomitant medications. - Evaluate renal function: adjust therapy if significant impairment exists. - Avoid use in patients with known hypersensitivity to ivacaftor. - Pregnancy and breastfeeding: discuss potential risks with a healthcare professional. - Store at ambient temperature: keep in the original container, protect from moisture and light.

What does Ivacaftor interact with?

Ivacaftor may interact with several medicines that affect its metabolism.

Major Interactions (Avoid): - Strong CYP3A inducers (e.g., rifampin, carbamazepine): may markedly reduce ivacaftor exposure. - Strong CYP3A inhibitors (e.g., ketoconazole, itraconazole): may increase ivacaftor levels and risk toxicity.

Moderate Interactions (Monitor Closely): - Azole antifungals (e.g., fluconazole): may raise ivacaftor concentrations; monitor clinical response. - Macrolide antibiotics (e.g., clarithromycin): can increase exposure; consider dose adjustment. - Oral contraceptives: ivacaftor may reduce efficacy; advise alternative or additional contraception methods.

Frequently asked questions

What is Ivacaftor Stada Nordic used for?+
Ivacaftor Stada Nordic contains ivacaftor, a CFTR potentiator indicated for the treatment of cystic fibrosis in patients who have specific gating mutations of the CFTR gene. It helps improve lung function and reduce disease‑related complications.
How does ivacaftor work in cystic fibrosis?+
Ivacaftor binds to the CFTR protein and stabilizes its open conformation, increasing the probability that the chloride channel remains open. This enhances chloride transport across epithelial cells, improving airway surface hydration and overall respiratory function.
What is the usual dose of ivacaftor?+
The dosage of ivacaftor is individualized and set by the prescribing healthcare professional based on the patient’s age, weight, specific CFTR mutation, and clinical condition. Patients should follow the prescriber’s instructions and not adjust the dose on their own.
Is ivacaftor safe during pregnancy or breastfeeding?+
Safety data for ivacaftor in pregnancy and lactation are limited. Women who are pregnant, planning to become pregnant, or breastfeeding should discuss potential risks and benefits with their healthcare provider before using the medication.
How do I order Ivacaftor Stada Nordic from GNH USA?+
To place an order, submit an enquiry on the product page at gnh-usa.com specifying 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, and any necessary import documentation.
How does ivacaftor compare with other cystic fibrosis treatments?+
Ivacaftor is a CFTR potentiator that directly enhances the function of defective CFTR proteins caused by gating mutations. Other therapies, such as correctors (e.g., lumacaftor) or combination regimens, target different mutation classes or mechanisms. The choice depends on the patient’s specific genetic profile and clinical needs.
What are the storage requirements for Ivacaftor Stada Nordic?+
Ivacaftor Stada Nordic should be stored at ambient temperature, below 25 °C, in its original packaging. Protect the product from moisture and direct light to maintain stability throughout its shelf life.
How is Ivacaftor Stada Nordic administered?+
The medication is taken orally, usually with a glass of water. The exact timing and whether it should be taken with food are determined by the prescribing clinician, who will provide specific instructions tailored to the patient’s regimen.
What are the most serious risks associated with ivacaftor?+
Serious risks include significant elevation of liver enzymes, development of cataracts, severe skin reactions, and rare cardiac arrhythmias. Patients should be monitored regularly for hepatic function, eye health, and any signs of hypersensitivity.
Who should not use ivacaftor?+
Ivacaftor is contraindicated in individuals with a known hypersensitivity to the drug or any of its excipients. Patients without a confirmed gating mutation of the CFTR gene should not use ivacaftor, as it would not provide therapeutic benefit.
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
Ivacaftor
Route
Oral Use
Manufacturer
Stada Nordic Aps
Origin
EU

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