GNH USA

Europe — EMA

Maraviroc Amarox Limited

GNH USA supplies Maraviroc Amarox Limited (Maraviroc), a CCR5 antagonist for HIV-1 infection in combination therapy. Request a quote for global supply.

Maraviroc

Request sourcing

1
Pack/s

What is Maraviroc?

Maraviroc, the active ingredient in Maraviroc Amarox Limited, is a CCR5 antagonist presented as an oral tablet for oral use. It is used in combination with other antiretroviral agents to treat HIV-1 infection in adults. GNH USA supplies Maraviroc Amarox Limited as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

What is Maraviroc used for?

Maraviroc is a CCR5‑targeting antiretroviral indicated for specific HIV‑1 treatment scenarios. - HIV‑1 infection (treatment‑experienced): added to a regimen of other antiretrovirals to achieve viral suppression. - CCR5‑tropic HIV‑1 infection: prescribed when the virus uses the CCR5 co‑receptor, confirmed by tropism testing. - Combination antiretroviral therapy: incorporated into multi‑drug regimens to reduce HIV viral load and improve immune recovery.

What are the side effects of Maraviroc?

Adverse reactions may vary in frequency and severity.

Common Side Effects: - Headache: mild to moderate intensity, often transient. - Nausea: occasional, may improve with food. - Diarrhea: watery stools, usually self‑limiting. - Fatigue: generalized tiredness. - Cough: dry or productive, non‑specific.

Serious or Rare Side Effects: - Hepatotoxicity: elevated liver enzymes or hepatitis. - Severe allergic reaction: rash, angioedema, or anaphylaxis. - QT interval prolongation: cardiac conduction changes. - Stevens‑Johnson syndrome/toxic epidermal necrolysis: severe skin reactions. - Immune reconstitution inflammatory syndrome: worsening of opportunistic infections after immune recovery.

What precautions apply to Maraviroc?

Before initiating therapy, clinicians should evaluate patient‑specific factors and monitor for potential risks. - Liver function monitoring: assess baseline enzymes and repeat periodically. - CCR5 tropism testing: confirm virus uses CCR5 before prescribing. - Avoid strong CYP3A4 inducers: may reduce drug exposure and efficacy. - Pregnancy and breastfeeding: safety not established; weigh benefits against risks. - Cardiovascular assessment: caution in patients with pre‑existing heart disease. - Store at below 25°C: keep in the original packaging, protect from moisture and direct sunlight.

What does Maraviroc interact with?

Maraviroc may interact with other medicines that affect its metabolism or transport.

Major Interactions (Avoid): - Rifampin: strong CYP3A4 inducer that markedly lowers maraviroc levels. - Carbamazepine: induces CYP3A4, reducing antiviral efficacy. - St. John’s wort: herbal inducer leading to decreased plasma concentrations.

Moderate Interactions (Monitor Closely): - Protease inhibitors (e.g., atazanavir): CYP3A4 inhibitors that can increase maraviroc exposure. - Azole antifungals (e.g., ketoconazole): may raise drug levels, requiring dose adjustment. - Macrolide antibiotics (e.g., erythromycin): can elevate plasma concentrations, necessitating monitoring.

Frequently asked questions

What is Maraviroc Amarox Limited used for?+
Maraviroc Amarox Limited contains the active ingredient maraviroc, a CCR5 antagonist indicated for the treatment of HIV‑1 infection when used in combination with other antiretroviral agents. It is prescribed for patients whose virus uses the CCR5 co‑receptor.
How does maraviroc work in the body?+
Maraviroc selectively binds to the CCR5 co‑receptor on CD4+ T cells, blocking the HIV‑1 envelope protein gp120 from attaching. This prevents the virus from entering the cell, thereby inhibiting replication and allowing the immune system to recover.
What is the usual dose of maraviroc?+
The dose of maraviroc is individualized by the prescribing clinician based on factors such as viral load, resistance profile, concomitant medications, and renal or hepatic function. Patients should follow the prescriber’s instructions and not adjust the dose on their own.
Is maraviroc safe during pregnancy or breastfeeding?+
The safety of maraviroc in pregnancy and lactation has not been definitively established. Healthcare providers must weigh potential benefits against unknown risks and discuss options with the patient. Breastfeeding decisions should consider the infant’s exposure.
How do I order Maraviroc Amarox Limited 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 maraviroc compare with other antiretroviral classes?+
Maraviroc belongs to the CCR5 antagonist class, which differs from nucleoside reverse transcriptase inhibitors, protease inhibitors, and integrase inhibitors. Its unique mechanism blocks viral entry rather than replication, making it useful for patients with CCR5‑tropic virus and as part of a diversified regimen.
What are the recommended storage conditions for Maraviroc Amarox Limited?+
Store the product at temperatures below 25 °C in its original container, protected from moisture and direct sunlight. Do not expose the tablets to excessive heat or humidity to maintain potency.
How is Maraviroc administered?+
Maraviroc is taken orally, usually as a tablet, with or without food as directed by the prescriber. The exact administration schedule (once or twice daily) depends on the individual treatment plan.
What are the most serious risks associated with maraviroc?+
Serious risks include hepatotoxicity, severe allergic reactions such as anaphylaxis, QT interval prolongation, and rare skin disorders like Stevens‑Johnson syndrome. Patients should be monitored for signs of liver dysfunction, cardiac abnormalities, and skin changes.
Who should not use maraviroc?+
Maraviroc is contraindicated in patients with known hypersensitivity to the drug or any of its components, and in those whose HIV‑1 strain does not use the CCR5 co‑receptor. It should also be avoided in patients taking strong CYP3A4 inducers without appropriate dose adjustment.
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
Amarox Limited
Origin
EU

Related products