Вотриент

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Вотриент

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Medically reviewed

Laura Arias

Last updated on 22/12/2025

This page provides general, reference-level information compiled from official medical sources. It is not a substitute for professional medical advice, diagnosis, or treatment. For decisions about your health, please consult a qualified healthcare professional.

Overview of Вотриент

Property Description
Active ingredient Pazopanib hydrochloride
Form Film-coated tablet
Pharmacological class Tyrosine Kinase Inhibitor (TKI)
General Purpose Antineoplastic agent (Cancer medicine)
Origin Synthetic, Small molecule

What Type of Medicine is Вотриент?

Вотриент is a specialized, prescription-only cancer medicine categorized as an antineoplastic agent. The drug's active ingredient is Pazopanib, which is formulated as Pazopanib hydrochloride. It is officially classified as a kinase inhibitor, a classification clinically recognized for its targeted mechanism against abnormal cell activity. Pazopanib belongs to the high-level pharmacological class of Tyrosine Kinase Inhibitors (TKIs), known specifically for functioning as a multi-target inhibitor against malignancy.

Composition, Form, and Origin of Pazopanib

The compound Pazopanib is a potent, synthetic, small molecule drug, distinguishing it from large biologic treatments. It is prepared for oral use as a distinctively colored film-coated tablet. Its oral administration via the film-coated tablet provides a defined route for systemic delivery, which is characteristic of this class of antineoplastic agents. As a single active ingredient product, the tablet contains only the Pazopanib hydrochloride component, underscoring its focused action profile.

What is the General Purpose of This Antineoplastic Agent?

The primary purpose of Вотриент is to help slow the progression of cancer by acting as a multi-target tyrosine kinase inhibitor. By selectively interfering with specific protein kinases, the medicine aims to disrupt the cell signaling that promotes proliferation and survival. The drug's mechanism involves the inhibition of the vascular endothelial growth factor receptors (VEGFRs). This targeted action is fundamental to its role as an antineoplastic agent, as it is designed to control tumor growth by restricting the blood supply (angiogenesis) required for rapid expansion, a strategy utilized in the management of solid tumors in adult patient groups.

Regulatory References

  1. Pazopanib Hydrochloride (NCI Drug Dictionary)

What side effects are possible with Вотриент?

Possible Side Effects and Safety Information

Regulatory documents classify the potential adverse effects of Pazopanib based on how frequently they appear in clinical studies. The official safety profile is defined by a range of effects across different body systems and specific safety constraints.

Frequency Classification and System-Organ Effects

Adverse reactions are grouped by System-Organ Class (SOC). Effects classified as Very Common (affecting more than 1 in 10 patients) include hypertension (high blood pressure), diarrhea, nausea, vomiting, fatigue, and changes in appearance such as hair color change and weight decreased. These are observed frequently in the vascular, gastrointestinal, and general disorders SOCs. Common effects include thrombocytopenia (low platelet count) and proteinuria (protein in urine).

Serious Adverse Reactions and Key Constraints

The label identifies several serious, clinically significant adverse reactions. These include a risk of severe and fatal hepatotoxicity (liver failure), serious hemorrhagic events, gastrointestinal perforation and fistula formation, and serious cardiac events such as QT prolongation. Furthermore, some risks are documented as being exposure-related; hypertension and elevated liver enzymes often occur early in the course of treatment.

Safety notes specify constraints for certain patient groups. Use is not recommended in patients with pre-existing severe hepatic impairment. A temporary interruption of therapy is advised prior to surgical procedures due to the risk of impaired wound healing, reflecting a major safety limitation documented in the official regulatory texts.

Overdose and Emergency Response

The official regulatory profile for Вотриент (Pazopanib) overdose is defined by the risk of severe exacerbation of known toxicities, which can be life-threatening. The specific clinical manifestation cited in overdose summaries is extreme tiredness.

Overdosage carries the potential for severe physiological events, including fatal hepatotoxicity, arterial thrombotic events, hemorrhagic events, and cardiac dysfunction such as a prolonged QT interval and Torsades de pointes. Gastrointestinal perforation and hypertensive crisis are also documented high-risk outcomes.

When a suspected overdose occurs, immediate medical intervention is required. Regulatory guidance mandates calling emergency services immediately if the affected individual has collapsed, had a seizure, has trouble breathing, or cannot be awakened. Individuals should also contact a regional Poison Control Center for guidance.

No specific antidote is known for Pazopanib overdosage. Treatment is therefore symptomatic and supportive, requiring close medical observation. Monitoring requirements include regular assessment of hepatic function, blood pressure, and cardiac function (ECGs and electrolytes). Patients with severe hepatic impairment are identified as a population with increased risk of toxicity.

Therapeutic Uses of Вотриент

Votrient is generally used in situations involving certain distressing symptoms related to advanced cancers. It is commonly used for adults with advanced renal cell carcinoma (RCC) and advanced soft tissue sarcoma (STS) in patients who have received prior chemotherapy. The core benefit plays a role in managing symptoms related to the progression of the disease and may assist with addressing symptoms related to heightened physiological activity.


Key Therapeutic Use and Benefits

This medication is primarily indicated for patients diagnosed with advanced RCC, a condition characterized by periods of heightened symptoms, and for advanced STS, particularly in scenarios where patients have previously received other systemic treatments. Votrient is relevant for easing symptoms that create noticeable physiological strain caused by advancing malignancy, such as physical discomfort and symptoms that interfere with daily functioning. The overarching patient benefit generally helps improve day-to-day comfort during symptomatic periods. This provides support that helps ease the overall symptom burden.

Quick Fact: Relief for Symptoms Related to Physical Discomfort

Eligibility and Restrictions for Use

Official Eligibility and Restrictions

Votrient (pazopanib) is indicated exclusively for the treatment of adult patients with advanced renal cell carcinoma (RCC) and advanced soft tissue sarcoma (STS) who have previously received chemotherapy. The official regulatory documents define clear eligibility boundaries based on age, organ function, and specific medical history.


Eligibility Status Patient Population/Condition
Contraindicated Patients with known hypersensitivity to pazopanib or any excipients.
Children younger than 2 years of age.
Not Recommended Patients with severe hepatic impairment (total bilirubin > 3 imes ULN).
Patients with severe renal impairment ( CrCl < 30 mL/min) or those undergoing dialysis.
Children and adolescents under 18 years due to insufficient safety data.
Conditional Use Patients with moderate hepatic impairment (requires careful monitoring).
Those with uncontrolled hypertension (blood pressure must be controlled prior to initiation).

Pregnancy and Lactation: The medicine is restricted in pregnancy due to the potential for fetal harm (FDA Pregnancy Category D). Use is not recommended while breastfeeding.

What should I know about interactions with other medicines?

Interactions with other medicines and products

The official interaction profile for Pazopanib ( Votrient^ extregistered) is defined by its susceptibility to metabolic and absorption changes, as documented in regulatory information. Co-administration with certain substances can significantly alter the drug's systemic exposure.

Pharmacokinetic and Food Interactions

Category Documented Interaction Outcome
Strong CYP3A4 Inhibitors (e.g., Ketoconazole) Increase pazopanib concentrations (uparrow AUC) [NIH DailyMed].
Strong CYP3A4 Inducers (e.g., Rifampin) Decrease pazopanib concentrations (downarrow AUC). Co-use is strongly advised against [FDA Label].
Drugs that Raise Gastric pH (e.g., PPIs, H2 receptor antagonists) Reduce pazopanib absorption and systemic exposure. Concomitant use should be avoided [FDA Label].
Food / Grapefruit Juice Food increases systemic exposure. Grapefruit juice, a CYP3A4 inhibitor, should be avoided [EMA SmPC].

Administration and Pharmacodynamic Constraints

The absorption interaction with food necessitates strict adherence to timing rules, requiring administration to occur without food (at least one hour before or two hours after a meal). Additionally, Pazopanib is an inhibitor of CYP2D6 and CYP2C8, which can increase the exposure of co-administered medicines that are substrates for these enzymes. A pharmacodynamic caution is documented for co-use with Simvastatin, which carries an increased risk of ALT elevations, and with other medicines that may prolong the QT interval [FDA Label].

Mechanism of Action

Blocking the Tyrosine Kinase Signaling System

Вотриент (Pazopanib) is a multi-target inhibitor that acts by binding within the ATP-binding pocket of several crucial Receptor Tyrosine Kinases (RTKs), including VEGFRs, PDGFRs, and c-Kit. This competitive interaction prevents the enzyme's autophosphorylation, thereby interrupting the transmission of signals that typically promote cellular proliferation and anti-apoptotic pathways. This molecular action restricts the unchecked signaling activity originating from these receptors.

Disrupting Malignant Tissue Support (Anti-Angiogenesis)

The systemic consequence of RTK inhibition is focused on the neoangiogenesis pathway. By targeting VEGFRs on vascular endothelial cells, the drug stops the signals necessary for the formation and proliferation of new blood vessels, a critical support structure for the malignant tissue structure. This action restricts the supply of oxygen and nutrients and supports the modification of tissue support dynamics, limiting the capacity for cellular proliferation and structural development.

Dosage and Administration Information

How to Use Вотриент (Pazopanib) - Administration Guidelines

Вотриент is an oral medication administered exclusively as a film-coated tablet. The drug is available in 200 mg and 400 mg strengths.


Standard Dosing and Administration Protocol

The standard initial recommended dose for adults is 800 mg once daily. The total dose must not exceed 800 mg. The medication is intended for continuous daily use until disease progression or development of unacceptable toxicity.

Procedural Instructions

  • Timing: The tablet must be taken without food, specifically at least one hour before or two hours after consuming a meal.
  • Tablet Integrity: The film-coated tablets must be swallowed whole with water and must not be crushed, chewed, or broken.
  • Missed Dose: If a dose is missed, it should not be taken if the time until the next scheduled dose is less than 12 hours.

Dose Adjustment Guidelines

Adjustments to the standard 800 mg dose, if necessary, should typically occur in 200 mg increments.

Population-Specific Dosing

  • Moderate Hepatic Impairment: The recommended dose is reduced to 200 mg once daily.
  • Severe Hepatic Impairment: Use is generally not recommended.

Recent Clinical Evidence

Research evidence / Overview of Studies for Votrient


Evidence for use in Advanced Renal Cell Carcinoma (Kidney Cancer)

This section will summarize the clinical trials and research studies that was evaluated in Votrient (pazopanib) for the indication of advanced kidney cancer, focusing on outcomes related to systemic or functional imbalance and the size and type of studies conducted.

Votrient was evaluated in major clinical trials involving patients with advanced kidney cancer (renal cell carcinoma). The research examined outcomes related to systemic or functional imbalance in these patients. The findings indicate that in the populations studied, Votrient was associated with specific patterns of change related to disease progression compared to other treatments or a placebo. The research describes patterns in outcomes in the observed populations in the setting of the clinical trials.

It is important to understand that the results apply only to the populations studied, and individual patient responses may vary significantly. Comparative evidence with every other existing treatment option is lacking, and research is ongoing.


Evidence for use in Advanced Soft Tissue Sarcoma (STS)

This section will outline the key studies that explored the use of Votrient for patients with certain types of advanced soft tissue sarcoma who have previously received chemotherapy, detailing the nature of the evidence available for this use.

Votrient was studied for certain advanced soft tissue sarcomas (STS). The evidence suggests that in the specific types of STS was observed in these trials, the medication was associated with certain measured differences in the research outcomes compared to placebo. The research provides insight into short-term changes in these outcomes.

For this use, the research does not determine whether an individual will respond similarly, as findings describe group patterns, not personal outcomes. It is noted that the sample sizes were modest for specific subtypes of soft tissue sarcoma, meaning the data for certain groups remain insufficient.


Long-term Studies and Follow-up

Some research has explored the outcomes related to Votrient beyond the initial treatment period. These studies monitored outcomes related to systemic or functional imbalance for an extended duration after the main trial was completed. These findings describe patterns observed in the studies regarding the patterns observed in outcomes over time.

However, follow-up durations were limited in many of the studies, meaning there is limited information for long-term outcomes that occur many years after the start of administration. As a result, long-term outcomes are not fully established.


What is Still Uncertain About Votrient

Despite the research that has been studied for Votrient, there are still areas where the evidence is limited or where more research is needed to provide greater clarity. The research provides context but not individual predictions for all scenarios. Certainty remains low in areas such as patterns of subsequent treatment. The research does not determine whether an individual will respond similarly to the group findings in every case, and further research is needed to fill these remaining gaps.

Frequently Asked Questions (FAQ)

Common questions about Вотриент (FAQ)


Q: Is Вотриент used as a first-line treatment or for later stages?

A: According to official regulatory documents, Вотриент is approved for the first-line treatment of advanced kidney cancer (renal cell carcinoma). For certain types of advanced soft tissue sarcoma (STS), its approved use is for adult patients who have received prior chemotherapy.


Q: How long do people typically stay on Вотриент treatment?

A: Official information states that the medication is intended for continuous daily use for as long as the disease does not progress or until the development of side effects that are considered unacceptable by the healthcare team. There is no set maximum duration for all patients.


Q: What are the signs of a possible liver problem while taking Вотриент?

A: The official label advises that healthcare providers should be contacted if signs of liver problems appear. These signs may include feeling pain or tenderness in the upper stomach, experiencing unusual tiredness, having dark urine, or noticing yellowing of the eyes or skin (jaundice). This is a serious, known risk that requires close monitoring.


Q: How is the blood pressure increase from Вотриент typically controlled?

A: High blood pressure is a common side effect, and regulatory advice emphasizes that blood pressure should be well controlled before starting treatment. If hypertension occurs during treatment, management may involve standard anti-hypertensive therapy and, if needed, a reduction or interruption of the Вотриент dose.


Q: Can patients with pre-existing heart conditions take Вотриент?

A: Official product information advises that Вотриент should be used with caution in patients who have a history of certain heart issues, such as QT interval prolongation or relevant pre-existing cardiac disease. Regulatory documents indicate that baseline and periodic monitoring of the heart's electrical activity (ECG) and electrolytes are recommended for these patients.


Q: Is it normal to have elevated thyroid hormone levels while on Вотриент?

A: Hypothyroidism, which is an underactive thyroid, is a common adverse reaction reported in clinical trials. Official guidance recommends that thyroid function tests should be performed at baseline and periodically monitored during treatment. Any identified dysfunction requires appropriate management.


Q: Can Вотриент be used to treat pediatric cancers?

A: The use of Вотриент is not recommended in children and adolescents under 18 years of age because the safety and effectiveness have not been established in this age group. The drug is contraindicated in children younger than 2 years of age.


Q: What should I do if a side effect from Вотриент becomes unmanageable?

A: Regulatory guidelines indicate that if adverse reactions occur, they may be managed with temporary interruption of therapy, a dosage reduction, or permanent discontinuation. These actions are determined by the treating physician and may include temporary interruption, dosage reduction, or permanent discontinuation.


Q: Does Вотриент treatment require frequent blood tests?

A: Yes, official safety information requires regular monitoring. This includes checking liver function tests frequently during the initial months and periodically afterward. Blood pressure and electrolytes also require routine monitoring as part of the treatment plan.


Q: Can I take Вотриент if I already have a history of blood clots?

A: Regulatory sources advise that the medication should be used with caution in patients who have a history of, or are at increased risk for, venous thrombotic events (blood clots). Your healthcare team will carefully assess the benefit versus risk in your specific case.


Q: Does taking Вотриент affect fertility in men or women?

A: Based on animal studies, official product information indicates that the drug may impair female fertility. While no impairment was observed in male animals, patients of reproductive potential should be made aware of the potential risks.


Q: Is it normal for my appetite to change after starting Вотриент?

A: Yes, decreased appetite is listed as a very common adverse reaction, meaning it was frequently observed in patients during clinical trials of the medication.


Q: Does weight gain or loss happen with Вотриент use?

A: Weight decreased is classified as a very common adverse reaction in the official product information, indicating it is an expected effect for many patients taking the medicine.


Q: Why do some people need a lower dose of Вотриент than others?

A: A dosage adjustment may be necessary for a few reasons, including managing adverse reactions or toxicity that a patient experiences. A reduced dose is also specifically recommended for patients who have moderate hepatic impairment (moderate liver problems).


Q: Can Вотриент affect wound healing?

A: Official safety constraints state that the drug may impair wound healing. Due to this risk, the therapy is recommended to be temporarily stopped, typically at least 7 days, before any scheduled surgical procedure.


Q: What common supplements or vitamins might interact with Вотриент?

A: The metabolism of Вотриент is affected by substances that influence the CYP3A4 enzyme, and regulatory information specifically advises that grapefruit or grapefruit juice should be avoided. Patients should communicate with their healthcare team about all supplements, vitamins, or herbal remedies they are considering, as these products may affect the drug’s concentration in the body.


Q: What kind of specialist usually prescribes and manages Вотриент treatment?

A: As a specialized anti-cancer agent, Вотриент treatment is typically managed by a physician experienced in the administration of anti-cancer medicines, usually as part of an oncology team or by a cancer specialist.


Q: Can I take pain relievers like Tylenol while on Вотриент?

A: While regulatory sources list many potential drug interactions based on metabolic pathways, a specific contraindication for Tylenol (acetaminophen) is not provided. Patients should communicate with their healthcare provider about all over-the-counter pain relievers or other medications taken, as this allows the care team to check for potential complex interactions.

How should Вотриент be stored and disposed of?

Storage and Disposal Requirements

Votrient (pazopanib) tablets must be stored according to strict regulatory specifications to maintain product quality.

Item Official Regulatory Requirement
Storage Temperature Store at controlled room temperature, typically 20 C to 25 C (68 F to 77 F). Do not freeze.
Protection & Packaging Store in the original container, tightly closed, to protect the tablets from moisture and direct light.
Child Protection The medicine must be kept out of the sight and reach of children at all times.
Disposal Instructions Unused or expired tablets must not be flushed down the toilet or placed in household trash. They should be returned to a drug take-back program or disposed of as instructed by a pharmacist.

Regulatory Storage Profile Summary: The official profile requires storing Votrient in its original packaging at a designated room temperature range while avoiding freezing, moisture, and excess heat. Disposal mandates the use of specialized channels to safely discard the medication, preventing environmental contamination.

Attention! Always consult to a doctor or pharmacist before using pills or medicines.

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