GNH USA

Europe — EMA

Maraviroc Tarbis

GNH USA supplies Maraviroc Tarbis (Maraviroc), a CCR5 antagonist for treatment of HIV‑1 infection in combination with other antiretroviral agents.

Maraviroc

Request sourcing

1
Pack/s

What is Maraviroc?

Maraviroc, the active ingredient in Maraviroc Tarbis, is a CCR5 antagonist presented as an oral formulation for oral use. It treats HIV‑1 infection in combination with other antiretroviral agents. Maraviroc works by blocking the CCR5 co‑receptor, preventing viral entry into CD4+ cells and reducing viral replication.

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

What is Maraviroc used for?

Maraviroc is a CCR5 antagonist used in the management of HIV‑1 infection.

- HIV‑1 infection (treatment‑naïve): reduces viral load when combined with standard antiretroviral regimens. - HIV‑1 infection (treatment‑experienced): provides an alternative mechanism for patients with resistance to other agents. - HIV‑1 infection (CCR5‑tropic virus): effective when the virus utilizes the CCR5 co‑receptor for cell entry.

What are the side effects of Maraviroc?

Common Side Effects: - Headache: mild to moderate intensity. - Nausea: may occur with or without vomiting. - Diarrhea: usually transient. - Fatigue: general tiredness. - Cough: dry or productive. - Rash: mild skin irritation.

Serious or Rare Side Effects: - Hepatotoxicity: elevated liver enzymes or hepatitis. - Severe allergic reaction: anaphylaxis, angioedema. - Depression or suicidal thoughts: monitor mental health. - QT interval prolongation: risk of cardiac arrhythmia. - Stevens‑Johnson syndrome: severe skin reaction. - Severe respiratory distress: rare pulmonary complications.

What precautions apply to Maraviroc?

Before initiating therapy, clinicians should assess patient suitability and monitor for adverse events.

- Liver function: evaluate baseline enzymes and monitor periodically. - Cardiac health: obtain ECG to assess QT interval, especially with other QT‑prolonging drugs. - Hypersensitivity: discontinue if signs of allergic reaction appear. - Pregnancy considerations: use only if potential benefit justifies potential risk. - Drug interactions: review concomitant medications for CYP3A4 modulators. - Store at ambient temperature: keep below 25°C, protect from moisture and light in the original packaging.

What does Maraviroc interact with?

Maraviroc may interact with several co‑administered medicines; careful review is required.

Major Interactions (Avoid): - Protease inhibitors (ritonavir, cobicistat): markedly increase maraviroc plasma levels. - Strong CYP3A inducers (rifampin, carbamazepine, phenytoin): substantially reduce exposure. - QT‑prolonging agents (quinidine, amiodarone): increase risk of cardiac arrhythmia.

Moderate Interactions (Monitor Closely): - Other antiretrovirals (efavirenz, nevirapine): may alter maraviroc concentrations. - Hepatitis C protease inhibitors (telaprevir, boceprevir): require dose adjustment. - Antacids containing aluminum or magnesium: may decrease absorption if taken simultaneously.

Frequently asked questions

What is Maraviroc Tarbis used for?+
Maraviroc Tarbis is prescribed as part of combination antiretroviral therapy for the treatment of HIV‑1 infection. It specifically targets viruses that use the CCR5 co‑receptor, helping to lower viral load and improve immune function when used with other approved HIV medicines.
How does Maraviroc work?+
Maraviroc blocks the CCR5 co‑receptor on CD4+ T‑cells, preventing the HIV‑1 envelope protein gp120 from binding. This inhibition stops the virus from entering the cell, thereby reducing replication of CCR5‑tropic HIV strains and contributing to viral suppression in patients receiving combination therapy.
What is the usual dose of Maraviroc Tarbis?+
The dosage of Maraviroc Tarbis is individualized by the prescribing clinician based on factors such as viral load, resistance profile, concomitant medications, and patient tolerance. Only a qualified healthcare professional should determine the appropriate dose and schedule.
Is Maraviroc safe during pregnancy or breastfeeding?+
Safety data for Maraviroc in pregnancy and lactation are limited. It should be used only if the potential maternal benefit outweighs any possible risk to the fetus or infant. Women who are pregnant, planning pregnancy, or breastfeeding should discuss risks and alternatives with their healthcare provider.
How do I order Maraviroc Tarbis 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 Maraviroc compare with other antiretroviral classes?+
Unlike nucleoside reverse transcriptase inhibitors or protease inhibitors, Maraviroc targets the CCR5 co‑receptor, offering a distinct mechanism that can be valuable for patients with resistance to other classes. It is used in combination regimens to broaden antiviral activity and may be preferred when the virus is confirmed to be CCR5‑tropic.
How should Maraviroc Tarbis be stored and handled?+
Maraviroc Tarbis should be stored at ambient temperature, preferably below 25 °C, in its original container to protect from moisture and light. Keep the product out of reach of children and avoid exposing it to excessive heat or humidity.
How is Maraviroc administered?+
Maraviroc is taken orally, usually with food to improve absorption. The tablet should be swallowed whole with a full glass of water and not crushed or chewed unless specifically instructed by a healthcare professional.
What are the most serious risks to watch for while taking Maraviroc?+
Serious risks include hepatotoxicity, severe allergic reactions such as anaphylaxis, depression or suicidal ideation, QT interval prolongation leading to cardiac arrhythmias, and rare but severe skin reactions like Stevens‑Johnson syndrome. Patients should report any unusual symptoms promptly to their clinician.
Who should not use Maraviroc Tarbis?+
Maraviroc is contraindicated in individuals with known hypersensitivity to maraviroc or any of its excipients. It should also be avoided in patients with severe liver impairment or those taking strong CYP3A inducers that would markedly reduce drug exposure, unless dose adjustments are made under 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
Maraviroc
Route
Oral Use
Manufacturer
Tarbis Farma, S.L.
Origin
EU

Related products