Registered Kenya · PPB

CELSENTRI 150MG TABLETS

MARAVIROC

H2008/19483/848 150MG NEW/INNOVATOR antiinfectives for systemic use INN generic

What it does

Maraviroc is a medication used to help manage HIV infection by blocking the virus from entering healthy cells.

Commonly used for: HIV infection (human immunodeficiency virus)

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Plain-language summary for general understanding - not medical advice. Always follow your pharmacist/doctor.

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Registration & product details

Registration no.
H2008/19483/848
Registration date
-
Expiry date
-
Status
Registered
Active ingredient
MARAVIROC
Dosage form
150MG
Strength
-
Pack size
30'S, 60'S,90'S180'S
Therapeutic class
NEW/INNOVATOR
ATC class (WHO)
J05AX - Other antivirals
RxNorm RxCUI
620216
Manufacturer / MAH
Laborex Kenya
Country of origin
FOREIGN
Manufacturer location
MV96+6MH Farm Auto spares building, Nairobi, Kenya

Source: Pharmacy and Poisons Board · fetched 2026-01-28 20:10:02 · updated 2026-08-03 04:10:20

Drug Interactions

14
Check interactions

Severe (2)

Fosamprenavir And Fosamprenavir Potentially Decreases The Exposure To Maraviroc - decreases exposure

Maraviroc potentially decreases the exposure to fosamprenavir and fosamprenavir potentially decreases the exposure to maraviroc. Avoid.

Severe Study

Maraviroc - decreases exposure

StJohn’swortispredictedtodecreasetheexposureto maraviroc.Avoid.rTheoretical

Severe Theoretical

Moderate (6)

Maraviroc - decreases exposure

Belzutifan is predicted to decrease the exposure to maraviroc. Avoid or adjust dose.

Moderate Theoretical

Maraviroc - decreases exposure

Cenobamateispredictedtodecreasetheexposureto maraviroc.Adjustdose.oTheoretical

Moderate Theoretical

Maraviroc - increases exposure

Idelalisibmarkedlyincreasestheexposuretomaraviroc. Adjustdose.rTheoretical

Moderate Theoretical

Maraviroc - decreases exposure

Mitotane is predicted to decrease the exposure to maraviroc. Adjust dose.

Moderate Study

Maraviroc - increases exposure

Vemurafenib is predicted to increase the exposure to maraviroc. Use with caution or avoid. Theoretical Measles, mumps and rubella vaccine, live → see live vaccines Mebendazole

Moderate Theoretical

Maraviroc - decreases exposure

Rifampicin is predicted to decrease the exposure to maraviroc. Adjust dose.

Moderate Study

Unknown (6)

Maraviroc - increases exposure

Cobicistat markedly increases the exposure to maraviroc. Refer to specialist literature.

Unknown Study

Maraviroc - decreases exposure

Bosentanispredictedtodecreasetheexposuretomaraviroc. Avoid.oTheoretical

Unknown Theoretical

Maraviroc - increases exposure

Atazanavir moderately to markedly increases the exposure to maraviroc. Refer to specialist literature.

Unknown Study

Maraviroc - increases exposure

Ritonavir markedly increases the exposure to maraviroc. Refer to specialist literature.

Unknown Study

Maraviroc - decreases exposure

Efavirenzdecreasestheexposuretomaraviroc.Referto specialistliterature.rTheoretical

Unknown Theoretical

Maraviroc - decreases exposure

Etravirine slightly decreases the exposure to maraviroc. Refer to specialist literature.

Unknown Study

Data from BNF 85 (British National Formulary). This is not a substitute for professional medical advice. Matched via: exact

Disclaimer: This information is sourced from Pharmacy and Poisons Board (Kenya). Always consult a qualified healthcare professional before using any medication.

About this medicine

Maraviroc is a medication used to help manage HIV infection by blocking the virus from entering healthy cells.

What it treats

  • HIV infection (human immunodeficiency virus)

How it works

It works by blocking certain receptors on the surface of cells that HIV uses to enter and infect them.

Who it's for

This medication is for adults and children who are infected with HIV and need treatment.

AI-assisted summary grounded in BNF data - general information only, not medical advice. Always confirm with your pharmacist or doctor.

Clinical monograph: Maraviroc

BNF-referenced

Maraviroc is a CCR5 antagonist used primarily in the treatment of HIV infection. It works by blocking the CCR5 co-receptor on the surface of T-cells, preventing HIV from entering and infecting these cells. This medication is particularly indicated for patients with CCR5-tropic HIV-1 strains who have experienced treatment failure with other antiretroviral therapies.

Indications

  • HIV infection resistant to other protease inhibitors
  • Combination therapy with other antiretroviral drugs in treatment-experienced patients with detectable CCR5-tropic HIV-1

Dosage

Children: Refer to the BNF for Children for appropriate dosing information.

Adults: 500 mg twice daily.

Mechanism of action

Maraviroc selectively binds to the CCR5 co-receptor on CD4+ T lymphocytes, inhibiting the entry of CCR5-tropic HIV-1 into these cells. This blockade prevents the virus from utilizing the CCR5 co-receptor necessary for its fusion and subsequent entry into the host cells, thus halting the infection process.

Pharmacodynamics

The pharmacodynamics of maraviroc involve its ability to selectively inhibit the binding of HIV to the CCR5 receptor, which is crucial for the virus's entry into immune cells. By preventing this interaction, maraviroc reduces the viral load and helps to preserve immune function in patients infected with CCR5-tropic HIV.

Pharmacokinetics

Maraviroc is well-absorbed when taken orally, with peak plasma concentrations occurring approximately 0.5 to 4 hours post-dose. It is extensively metabolized by the liver, primarily through CYP3A4, and has a half-life of about 14 to 18 hours. The drug is primarily excreted through feces, with renal excretion accounting for a small percentage. Liver function should be monitored due to potential hepatotoxic effects.

Adverse effects

  • Abdominal pain
  • Anaemia
  • Appetite decreased
  • Asthenia
  • Depression
  • Diarrhoea
  • Flatulence
  • Headache
  • Insomnia
  • Nausea
  • Rash
  • Hyperamylasaemia
  • Influenza-like illness
  • Dehydration
  • Hyperbilirubinaemia
  • Intracranial haemorrhage
  • Bleeding tendency

Interactions

  • Maraviroc + fosamprenavir: severe (decreases exposure)
  • St. John's Wort + maraviroc: severe (decreases exposure)
  • Belzutifan + maraviroc: moderate (decreases exposure)
  • Cenobamate + maraviroc: moderate (decreases exposure)
  • Idelalisib + maraviroc: moderate (increases exposure)
  • Mitotane + maraviroc: moderate (decreases exposure)
  • Vemurafenib + maraviroc: moderate (increases exposure)
  • Rifampicin + maraviroc: moderate (decreases exposure)
  • Cobicistat + maraviroc: unknown (increases exposure)
  • Bosentan + maraviroc: unknown (decreases exposure)

Precautions

  • Caution in patients with abnormal liver function tests or signs of liver injury
  • Monitor liver function before treatment, then every 2 weeks for 3 months, then monthly until 48 weeks, then every 8 to 12 weeks thereafter
  • Caution in patients with renal impairment (eGFR less than 80 mL/minute/1.73 m2)
  • Consider delaying treatment if serum transaminases are greater than 5 times the upper limit of normal

Pregnancy

Manufacturer advises use only if potential benefit outweighs risk due to toxicity in animal studies.

Breast-feeding

Unknown, consult product literature.

Storage

Store in a cool, dry place, protected from light.

Formulations

  • Maraviroc 25 mg tablets
  • Maraviroc 75 mg tablets
BNF 85 (British National Formulary) p.744 BNF for Children 2019-2020 p.465 PubChem / pathway

AI-synthesized from BNF references - general information only, not a substitute for professional medical advice or the current BNF. Verify doses with a pharmacist.

Molecular reference: Maraviroc

PubChem CID 3002977

Molecular formula: C29H41F2N5O

Source: PubChem (NCBI) · pathways from PathBank, Reactome, WikiPathways & PharmGKB.