GNH USA

Europe — EMA

Nintedanib Stada

GNH USA supplies Nintedanib Stada (Nintedanib), a tyrosine kinase inhibitor for idiopathic pulmonary fibrosis, systemic sclerosis‑associated ILD and NSCLC

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What is Nintedanib?

Nintedanib, the active ingredient in Nintedanib Stada, is a tyrosine kinase inhibitor presented as an oral formulation for oral use. It is indicated for idiopathic pulmonary fibrosis, systemic sclerosis‑associated interstitial lung disease, and in combination with docetaxel for non‑small cell lung cancer.

GNH USA supplies Nintedanib Stada as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres and pharmacies worldwide.

What is Nintedanib used for?

Nintedanib acts on multiple receptor tyrosine kinases involved in fibrotic and oncologic pathways. - Idiopathic pulmonary fibrosis: slows the decline in lung function and reduces disease progression. - Systemic sclerosis‑associated interstitial lung disease: improves forced vital capacity and delays worsening of respiratory symptoms. - Non‑small cell lung cancer (with docetaxel): enhances overall response rates and prolongs progression‑free survival when added to chemotherapy.

What are the side effects of Nintedanib?

Nintedanib is associated with a range of adverse reactions that vary in frequency and severity.

Common Side Effects: - Diarrhea: frequent, often mild to moderate in intensity. - Nausea and vomiting: may occur early in treatment. - Decreased appetite: can contribute to weight loss.

Serious or Rare Side Effects: - Elevated liver enzymes or hepatitis: monitor hepatic function regularly. - Bleeding events: increased risk of gastrointestinal or other hemorrhage. - Cardiovascular events: includes hypertension and rare myocardial infarction.

What precautions apply to Nintedanib?

Before initiating therapy, clinicians should assess individual risk factors and monitor key parameters. - Pregnancy: contraindicated; avoid use during pregnancy and advise effective contraception. - Liver function: obtain baseline tests and repeat periodically; adjust if significant elevation occurs. - Bleeding risk: evaluate concomitant anticoagulant or antiplatelet therapy. - Cardiovascular health: monitor blood pressure and cardiac status, especially in patients with pre‑existing disease. - Drug interactions: review concomitant medications that affect CYP3A4 or P‑glycoprotein. - Store at ambient temperature: keep below 25 °C, in the original container, protected from moisture and light.

What does Nintedanib interact with?

Nintedanib may interact with several drug classes, requiring careful management.

Major Interactions (Avoid): - Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): may increase nintedanib exposure. - Strong CYP3A4 inducers (e.g., rifampin, carbamazepine): may reduce therapeutic effect. - P‑glycoprotein inhibitors (e.g., verapamil): can raise plasma concentrations.

Moderate Interactions (Monitor Closely): - Anticoagulants (e.g., warfarin, direct oral anticoagulants): heightened bleeding risk. - Antiplatelet agents (e.g., aspirin, clopidogrel): may augment hemorrhagic events. - Diuretics: monitor electrolytes and renal function due to potential additive effects on fluid balance.

Frequently asked questions

What conditions is Nintedanib Stada used to treat?+
Nintedanib Stada is prescribed for idiopathic pulmonary fibrosis, systemic sclerosis‑associated interstitial lung disease, and for non‑small cell lung cancer when used together with docetaxel. In each case the drug targets pathways that drive fibrosis or tumor angiogenesis, helping to slow disease progression.
How does the active ingredient nintedanib work in the body?+
Nintedanib blocks the activity of several receptor tyrosine kinases, including VEGFR, PDGFR and FGFR. By inhibiting these signals it reduces fibroblast growth, migration and transformation, and also limits new blood‑vessel formation, which together mitigate fibrotic tissue buildup and tumor vascular support.
What is the usual dose of Nintedanib Stada?+
The specific dose and dosing schedule of Nintedanib Stada are determined by the prescribing clinician based on the patient’s condition, weight, renal and hepatic function, and other individual factors. Healthcare professionals should follow the approved prescribing information for each indication.
Is Nintedanib Stada safe to use during pregnancy or breastfeeding?+
Nintedanib Stada is contraindicated in pregnancy because it may cause fetal harm. Women of childbearing potential should use effective contraception. Safety during breastfeeding has not been established, so nursing mothers should avoid the medication unless the benefits outweigh the risks.
How do I order Nintedanib Stada 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 (including any cold‑chain requirements) and necessary import documentation.
How does Nintedanib Stada compare with other antifibrotic agents?+
Nintedanib differs from other antifibrotics such as pirfenidone by targeting a broader range of tyrosine kinases (VEGFR, PDGFR, FGFR). This multi‑target approach can offer additional benefit in certain fibrotic lung diseases, though the safety profile and tolerability may vary, requiring individualized assessment by the treating physician.
What are the recommended storage conditions for Nintedanib Stada?+
Nintedanib Stada should be stored at ambient temperature, below 25 °C, in its original packaging. Keep the product away from moisture, direct sunlight and excessive heat to maintain stability throughout its shelf life.
How is Nintedanib Stada administered to patients?+
The medication is taken orally, usually with food to lessen gastrointestinal discomfort. Patients should swallow the tablet whole with a full glass of water and follow the dosing schedule prescribed by their healthcare provider.
What are the most serious risks associated with Nintedanib Stada?+
The most serious risks include significant liver injury, severe bleeding events, and cardiovascular complications such as hypertension or myocardial infarction. Patients should be monitored regularly for liver enzyme elevations, signs of hemorrhage, and changes in blood pressure.
Who should not use Nintedanib Stada?+
Nintedanib Stada should not be used by pregnant women, individuals with severe hepatic impairment, or patients with uncontrolled bleeding disorders. It is also contraindicated in patients who are hypersensitive to nintedanib or any of the tablet’s excipients.
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
Nintedanib
Route
Oral Use
Manufacturer
Stada Arzneimittel Ag
Origin
EU

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