Flovent
Flovent
Generic Name
Flovent
Mechanism
- Glucocorticoid receptor activation: Intracellular uptake → translocation to the nucleus → binding to glucocorticoid response elements (GREs).
- Transrepression & transactivation: ↓ Pro‑inflammatory cytokines (IL‑4, IL‑5, IL‑13), ↑ anti‑inflammatory proteins (IL‑1 receptor antagonist, lipocortin‑1).
- ↓ Leukocyte migration to bronchial mucosa, ↓ mast cell degranulation, ↓ smooth‑muscle hyperplasia.
- Result: ↓ airway hyperresponsiveness, mucus production, and bronchial edema.
Pharmacokinetics
- Absorption: Delivered via dry powder; systemic absorption ≈ 3–8 % of a single dose.
- Distribution: Widely distributed; plasma protein binding > 99 %.
- Metabolism: Hepatic CYP3A4 → inactive metabolites.
- Excretion: Urine and feces; elimination half‑life 7–8 h for plasma, but pulmonary residence > 12 h.
- Drug interactions: CYP3A4 inhibitors (ketoconazole, ritonavir) increase systemic exposure; concurrent oral steroids potentiate adrenal suppression.
Indications
- Asthma – Maintenance therapy (daily prophylaxis).
- COPD – Reliever of exacerbations when combined with long‑acting β₂‑agonists (LABAs).
- Allergic rhinitis & nasal polyposis – Off‑label use in some jurisdictions.
Contraindications
- Absolute contraindications:
- Known hypersensitivity to fluticasone or any component.
- Active systemic infection requiring oral steroids.
- Warnings:
- Potential for adrenal suppression (≥ 2 % systemic exposure).
- Osteoporosis, cataracts, and growth retardation in pediatric patients.
- Susceptibility to oral thrush; maintain oral hygiene.
- Precautions:
- Use at lowest effective dose.
- Avoid in patients on potent CYP3A4 inhibitors unless dose adjustment is guided.
Dosing
| Age Group | Standard Dose (daily) | Titration |
| Adults & Adolescents ≥ 12 yr | 200 µg twice daily (400 µg/day) | Increase to 400 µg BID (800 µg/day) if control inadequate |
| Children 6–11 yr | 100 µg BID | Titrate cautiously; monitor growth |
| Children < 6 yr | Not approved | Use other formulation or drug |
• Technique – Exhale fully, place inhaler mouthpiece in mouth, inhale slowly while activating device, hold breath 5 s.
• Spacer use – Reduces oropharyngeal deposition, beneficial for children and patients with coordination issues.
• Reconstitution – Not required; pre‑filled dry powder device.
Adverse Effects
- Common
- Oral candidiasis (hoarseness, taste alteration)
- Dysphonia, cough, sore throat
- Nasal irritation (if using nasal spray)
- Serious
- Systemic corticosteroid effects: adrenal suppression, glucose intolerance, osteoporosis.
- Growth retardation (pediatric) – monitor height/weight annually.
- Rare: Angioedema, severe allergic reaction.
Monitoring
- Pulmonary function – Peak expiratory flow (PEF) or FEV₁ every 6 – 12 weeks.
- Growth metrics (children) – Height percentile tracking.
- Adrenal axis – Dexamethasone suppression test if systemic exposure suspected.
- Bone density – Baseline DEXA scan for chronic high‑dose users > 5 yr.
- Oral hygiene – Daily mouthwash or fluoride rinse; check for thrush.
Clinical Pearls
- Dry‑powder advantage – Faster onset, less throat irritation than nebulized or metered‑dose solutions.
- Avoid oral steroids unless needed – Use Flovent first to reduce systemic burden.
- Spacer is key for kids – Improves dose delivery to the lungs and reduces dysphonia.
- Low‑dose strategy – Start 100 µg BID in children; many achieve control at ≤ 200 µg/day.
- Monitoring growth – Even moderate doses show transient catch‑up; severe growth delay is rare with proper dosing.
- When using CYP3A4 inhibitors – Consider 300 µg/day if patient requires a strong inhibitor; monitor for adrenal signs.
- Post‑inhalation rinsing – Rinse mouth with water after each dose to mitigate thrush.
- Use same device – Switching between inhalers frequently impairs technique and therapeutic efficacy.
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• *Flovent* remains the cornerstone of inhaled corticosteroid therapy for asthma and COPD control. Proper dosing, vigilant monitoring, and patient education are essential to maximize benefit and minimize adverse events.