GNH USA

Europe — EMA

Nexavar (Sorafenib)

GNH USA supplies Nexavar (Sorafenib), a multi‑kinase inhibitor for renal cell carcinoma, hepatocellular carcinoma and other advanced cancers.

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What is Sorafenib?

Sorafenib, the active ingredient in Nexavar, is a multi-kinase inhibitor presented as a tablet for oral use. It treats certain advanced cancers such as renal cell carcinoma, hepatocellular carcinoma, differentiated thyroid carcinoma, and advanced gastrointestinal stromal tumor in adult patients.

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

What is Sorafenib used for?

Sorafenib is used to target malignant tumors that rely on kinase‑driven proliferation and angiogenesis.

Renal cell carcinoma: prolongs progression‑free survival in advanced disease. Hepatocellular carcinoma: improves overall survival in patients with unresectable disease. Differentiated thyroid carcinoma: delays disease progression in radioactive‑iodine‑refractory cases. Advanced gastrointestinal stromal tumor: provides disease control after failure of prior tyrosine‑kinase inhibitors.

What are the side effects of Sorafenib?

Sorafenib may cause a range of adverse reactions that vary in frequency and severity.

Common Side Effects: - Diarrhea - Hypertension - Fatigue - Rash

Serious or Rare Side Effects: - Severe bleeding - Hepatic failure - Cardiac ischemia

What precautions apply to Sorafenib?

When prescribing Sorafenib, clinicians should consider several safety measures.

Monitor blood pressure: check regularly and manage hypertension. Assess liver function: perform baseline and periodic tests. Evaluate cardiac status: monitor for ischemic events. Review wound healing: delay elective surgery if possible due to anti‑angiogenic effect. Store at ambient temperature: keep below 25°C in the original container, protect from moisture.

What does Sorafenib interact with?

Sorafenib can interact with other medicines, requiring careful management.

Major Interactions (Avoid): - Strong CYP3A4 inducers (e.g., rifampin): reduce Sorafenib exposure. - Antiplatelet agents (e.g., aspirin): increase bleeding risk. - QT‑prolonging drugs (e.g., sotalol): may exacerbate cardiac risk.

Moderate Interactions (Monitor Closely): - CYP3A4 inhibitors (e.g., ketoconazole): increase Sorafenib levels. - H2 blockers or PPIs: may affect absorption. - Statins metabolized by CYP3A4 (e.g., simvastatin): consider dose adjustment.

Frequently asked questions

What conditions is Nexavar used to treat?+
Nexavar (Sorafenib) is indicated for adult patients with advanced renal cell carcinoma, unresectable hepatocellular carcinoma, radioactive‑iodine‑refractory differentiated thyroid carcinoma, and advanced gastrointestinal stromal tumor after prior therapy. It targets cancers that depend on kinase‑driven growth and blood‑vessel formation.
How does Sorafenib work in the body?+
Sorafenib blocks several key kinases such as RAF, VEGFR‑2, VEGFR‑3, PDGFR‑β, FLT‑3 and c‑KIT. Inhibiting these enzymes interferes with tumor cell proliferation and the formation of new blood vessels, thereby slowing tumor growth and spread.
What is the usual dose of Nexavar?+
The specific dosage and schedule of Nexavar are determined by the prescribing physician based on the patient’s condition, weight, liver function and other clinical factors. Patients should follow the exact regimen provided by their healthcare professional.
Is Nexavar safe during pregnancy or breastfeeding?+
Nexavar is classified as Pregnancy Category X, indicating it is contraindicated in pregnancy because it can cause fetal harm. It is also not recommended for breastfeeding mothers, as it may be excreted in milk and affect the infant.
How do I order Nexavar from GNH USA?+
To request Nexavar, 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 Nexavar compare with other treatments for the same cancers?+
Nexavar belongs to the multi‑kinase inhibitor class, offering a distinct mechanism from monoclonal antibodies or pure VEGF inhibitors. Compared with some alternatives, it targets a broader range of kinases, which can be advantageous in tumors that develop resistance to single‑target agents, though safety profiles differ.
What are the storage requirements for Nexavar tablets?+
Nexavar tablets should be stored at ambient temperature, preferably below 25 °C. Keep them in the original packaging, protect from moisture and direct sunlight, and store out of reach of children.
How is Nexavar administered?+
Nexavar is taken orally as a tablet, usually with a glass of water. The tablet should be swallowed whole and not crushed or chewed, unless the prescriber provides specific instructions.
What are the most serious risks associated with Nexavar?+
Serious risks include severe bleeding, hepatic failure, and cardiac ischemia. Patients should be monitored closely for signs of gastrointestinal hemorrhage, liver enzyme elevations, and chest pain or other cardiac symptoms, and treatment should be adjusted or discontinued if these occur.
Who should not use Nexavar?+
Nexavar should not be used by patients who are pregnant, breastfeeding, have uncontrolled hypertension, severe hepatic impairment, or a history of significant cardiac ischemia. It is also contraindicated in individuals taking strong CYP3A4 inducers without medical supervision.
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
Sorafenib
Route
Oral Use
Manufacturer
Bayer Ag
Origin
EU

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