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← New search | Fluticasone furoate/ Vilanterol Trifenatate

INN monograph

Fluticasone furoate/ Vilanterol Trifenatate

Corticosteroid · POM

POM Source-linked Grade A-

Source-linked · Updated 03 Aug 2026 · Source: Local active-ingredient clinical extract; FDA drug label via OpenFDA/DailyMed; Professional class pharmacology (Corticosteroid)

Kenya market

Wholesale / list prices where loaded

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Median
Brands
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Risk first

Contraindications

  • Systemic fungal infections (untreated) for systemic steroids.
  • Live vaccines with significant immunosuppression.
  • Hypersensitivity.
  • Topical: untreated skin infection at site (relative).

Precautions

  • Warnings Only for use in the nose.
  • Do not spray into your eyes or mouth.
  • Do not use • in children under 2 years of age • to treat asthma • if you have an injury or surgery to your nose that is not fully healed • if you have ever had an allergic reaction to this product or any of the ingredients Ask a doctor before use if you have or had glaucoma or cataracts Ask a doctor or pharmacist before use if you are taking • medicine for HIV infection (such as ritonavir) • a steroid medicine for asthma, allergies or skin rash • ketoconazole pills (medicine for fungal infection) When using this product • the growth rate of some children may be slower • stinging or sneezing may occur for a few seconds right after use • do not share this bottle with anyone else as this may spread germs • remember to tell your doctor about all the medicines you take, including this one Stop use and ask a doctor if • you have, or come into contact with someone who has, chicken pox, measles or tuberculosis • your symptoms do not get better within 7 days of starting use or you get new symptoms such as severe facial pain or thick nasal discharge.
  • You may have something more than allergies, such as an infection. • you get a constant whistling sound from your nose.
  • This may be a sign of damage inside your nose. • you get an allergic reaction to this product.
  • Seek medical help right away. • you get new changes to your vision that develop after starting this product • you have severe or frequent nosebleeds If pregnant or breast-feeding, ask a health professional before use.
  • Keep out of reach of children.
  • In case of overdose, get medical help or contact a Poison Control Center right away.

Point of care

Dosing

Adult

Directions • read the Quick Start Guide for how to: • shake vigorously before each use • prime the bottle • use the spray • sniff gently after each spray • clean the spray nozzle with a clean dry tissue • use this product only once a day • do not use more than directed ADULTS AND CHILDREN 12 YEARS OF AGE AND OLDER • Week 1 – use 2 sprays in each nostril once daily • Week 2 through 6 months – use 1 or 2 sprays in each nostril once daily, as needed to treat your symptoms • After 6 months of daily use – ask your doctor if you can keep using CHILDREN 2 TO 11 YEARS OF AGE • the growth rate of some children may be slower while using this product. Children should use for the shortest amount of time necessary to achieve symptom relief. Talk to your child’s doctor if your child needs to use the spray for longer than two months a year. • an adult should supervise use • use 1 spray in each nostril once daily CHILDREN UNDER 2 YEARS OF AGE • do not use

Paediatric

See label paediatric section if present; otherwise use paediatric formulary — do not extrapolate adult doses.

Renal

Fluid retention/hypertension — care in renal disease.

  • CrCl 0–120: Confirm renal dosing in product SmPC / primary label.

Hepatic

Prednisone needs hepatic activation to prednisolone.

Safety

Drug interactions

Open checker →
  • State indication and planned duration on every prescription.
  • Bone protection if prolonged.
  • Screen for strongyloides risk before prolonged high-dose in endemic exposure.
  • ICS: spacer + rinse mouth.

Safety

Adverse effects

  • Insomnia, increased appetite, mood lability, dyspepsia, hyperglycaemia.
  • Chronic: cushingoid features, myopathy, osteoporosis, HPA suppression.
  • Topical: skin atrophy, striae.
  • Inhaled: thrush, dysphonia.

Use

Indications

  • Uses Temporarily relieves these symptoms of hay fever or other upper respiratory allergies: • nasal congestion • runny nose • sneezing • itchy nose • itchy, watery eyes (for ages 12 and older) Clinical selection for Fluticasone furoate/ Vilanterol Trifenatate should follow culture results where relevant, Kenya STG/EML recommendations, and the current product SmPC.
  • Class context: Corticosteroid.
  • Confirm site-specific dose, duration and monitoring before prescribing.

Pharmacology

Mode of action

Long-acting beta-2-agonist and inhaled corticosteroid.

Stimulate β2 receptors ↑ cAMP Bronchodilation
Full mechanism text

Long-acting beta-2-agonist and inhaled corticosteroid. Corticosteroids bind intracellular glucocorticoid receptors, modulating gene transcription to suppress inflammatory cytokines, inhibit phospholipase A2 via lipocortins, reduce leukocyte migration and stabilise membranes — potent anti-inflammatory and immunosuppressive effects. Mineralocorticoid activity varies by agent.

ADME

Pharmacokinetics & PD

Onset Hours–days
Duration Agent and route dependent
Route ORAL / IV / IM / INHALED / TOPICAL / NASAL / OPHTHALMIC
Full PK/PD text

Systemic agents: good absorption, hepatic metabolism, variable half-lives (dexamethasone long). Inhaled/topical: designed to minimise systemic exposure but high-dose/long duration still risks adrenal suppression.

Kenya

Brands & prices

0 listed
Brand Company Pack KES
No brands linked yet.

Special populations

Pregnancy & lactation

Pregnancy

Used when maternal benefit clear; prefer agents with better obstetric data (e.g. prednisolone). Document risk–benefit.

Lactation

Low-dose systemic often compatible; time feeds if high dose — agent-specific.

Diet

Food & alcohol

  • Food
  • Food

Trust

Sources & disclaimer

Source: Local active-ingredient clinical extract; FDA drug label via OpenFDA/DailyMed; Professional class pharmacology (Corticosteroid)

Open source link

Clinical review date not recorded.

Decision support only — not a substitute for clinical judgment, product SmPC, or Kenya STG/EML.

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