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Mometasone

Corticosteroid · Anti-inflammatory, Anti-allergic, Antiasthmatic, Dermatological agent

Also known as Mometasone Furoate, Nasonex, Elocon, Asmanex Twisthaler

START
Confirm allergic rhinitis, asthma, or dermatologic indication. Rule out active nasal/oral infection. For asthma: ensure NOT for acute bronchospasm. Teach proper inhaler/spacer technique.
TYPICAL MAX
880 mcg BID (inhalation); 200 mcg/nostril/day (nasal). Do not exceed.
STOP IF
Severe nasal bleeding, signs of adrenal suppression (fatigue, weakness, weight loss, hypotension), severe allergic reaction, worsening of untreated infection
WATCH
Growth velocity in children (stadiometry every 6 months), signs of candidiasis (inhalation — rinse mouth after use), intraocular pressure (annual eye exam with prolonged use), nasal mucosa integrity
CDSCO approvedJan AushadhiATC R01AD09
Dose laddermg/d
50start100titrate220titrate880ceiling
Renal dose adjustmenteGFR mL/min/1.73m²
FULLNo adjustment required1590

KDIGO 2024 + manufacturer label

Pharmacokineticsplasma · t hours
1dONSET2wPEAK5.8h1dDURATION
ONSET
1d · 1-2 days (nasal); 1-2 weeks (inhalation)
PEAK
2w · 1-2 weeks (max effect)
5.8h · ~5.8 h (absorbed fraction)
DURATION
1d · 24 h (nasal/topical); 12 h (inhalation BID)
EXCRETION
Biliary/fecal (metabolites); <1% renal; extensive first-pass
route + CYP
INTERACTIONS
none in our sources
PREGNANCY
FDA PLLR: Animal studies showed fetal harm at high systemic doses. Limited human data. Use during pregnancy only if benefit clearly outweighs risk. Budesonide has the most safety data in pregnancy among inhaled corticosteroids.
FDA category + note
Available in India

281 branded formulations and 358 fixed-dose combinations. Look up specific brands in the Drugs workspace.

Jan Aushadhi — generic available at GoI pharmacies

Mechanism

Mometasone furoate is a synthetic corticosteroid with potent anti-inflammatory, anti-allergic, and vasoconstrictive properties. It binds to intracellular glucocorticoid receptors (GR) in target cells, forming a steroid-receptor complex that translocates to the nucleus and modulates gene transcription. This results in: (1) inhibition of phospholipase A2, reducing arachidonic acid release and downstream prostaglandin and leukotriene synthesis; (2) suppression of inflammatory cytokine production (IL-1, IL-2, IL-6, TNF-alpha, IFN-gamma); (3) decreased mast cell and eosinophil recruitment; and (4) reduced vascular permeability. Mometasone has a high topical-to-systemic potency ratio due to extensive first-pass hepatic metabolism and low systemic bioavailability.

Indications

Allergic rhinitis (nasal spray)Nasal polyps (prophylaxis/treatment)Asthma prophylaxis (inhalation — maintenance only, not acute bronchospasm)Dermatitis, eczema, psoriasis (topical cream/ointment/lotion)Chronic obstructive pulmonary disease (COPD) maintenance (off-label, inhalation)

Dosing

Adult
Allergic rhinitis: 2 sprays (100 mcg) in each nostril daily; maintenance: 1 spray (50 mcg) in each nostril daily. Nasal polyps: 2 sprays in each nostril BID. Asthma: 220-440 mcg inhalation BID (max 880 mcg BID). Topical: apply thin layer to affected area daily.
Pediatric
Allergic rhinitis (2-11 years): 1 spray (50 mcg) in each nostril daily. (12+ years): adult dosing. Asthma (4-11 years): 110 mcg BID. Topical (≥2 years): apply thin layer daily.
Renal adjustment
No adjustment required.
Hepatic adjustment
No adjustment required (extensive first-pass metabolism but minimal systemic exposure).
Geriatric
No specific adjustment. Monitor for systemic corticosteroid effects with prolonged high-dose use.
Max dose
880 mcg BID (inhalation); 200 mcg/nostril/day (nasal)

Pharmacokinetics

Onset
Nasal: 1-2 days for symptom relief. Inhalation: 1-2 weeks for asthma control. Topical: 2-3 days for skin improvement.
Peak effect
Nasal: 1-2 weeks (maximum effect). Inhalation: 1-2 weeks.
Duration
24 hours (nasal, topical); 12 hours (inhalation BID).
Half-life
~5.8 hours (plasma elimination; reflects absorbed fraction).
Bioavailability
Nasal: <1% (oral bioavailability of swallowed portion). Inhalation: <1% (oral bioavailability of swallowed portion). Topical: <0.4% (percutaneous absorption).
Protein binding
~98-99% (bound to albumin).
Metabolism
Extensive hepatic first-pass metabolism via CYP3A4 (primary) to multiple metabolites. No active metabolites. 5-beta-hydroxy and delta-1,2-dehydro metabolites are primary.
Excretion
Biliary/fecal (major, as metabolites). Renal: <1% (as metabolites).

Contraindications

  • Hypersensitivity to mometasone or any component
  • Untreated localized nasal, oral, or systemic infections (bacterial, fungal, viral including herpes simplex, TB)
  • Status asthmaticus or acute asthma attack (inhalation)
  • Recent nasal surgery/trauma (nasal spray — until healed)

Side effects

Common
Nasal irritation, burning, dryness, epistaxis (nasal spray)Oropharyngeal candidiasis (inhalation)Hoarseness, dysphonia (inhalation)Skin atrophy, thinning, striae (prolonged topical use)Headache
Serious
  • Adrenal suppression/HPA axis suppression (with prolonged high-dose systemic absorption)
  • Growth retardation in children (chronic high-dose inhalation/nasal)
  • Glaucoma, cataracts (prolonged use — especially with high-dose inhaled/nasal)
  • Septal perforation (nasal spray — rare)
  • Increased susceptibility to infections (localized immunosuppression)
  • Psychiatric effects (mood changes, depression, aggression — rare with inhaled corticosteroids)

Pregnancy & lactation

Pregnancy

FDA PLLR: Animal studies showed fetal harm at high systemic doses. Limited human data. Use during pregnancy only if benefit clearly outweighs risk. Budesonide has the most safety data in pregnancy among inhaled corticosteroids.

Lactation

Minimal systemic absorption means negligible excretion in breast milk. Compatible with breastfeeding per AAP. Monitor infant for thrush if using inhalation.

Drug interactions

Cobicistat
Moderate
Database

Increased systemic exposure to mometasone, potentially leading to Cushing's syndrome or adrenal suppression, especially with prolonged use or high doses.

Monitor for signs of systemic corticosteroid effects. Consider reducing mometasone dose or using an alternative antiretroviral if prolonged co-administration is necessary. Use with caution.

Itraconazole
Moderate
Database

Increased systemic exposure to mometasone, potentially leading to Cushing's syndrome or adrenal suppression, especially with prolonged use or high doses.

Monitor for signs of systemic corticosteroid effects. Consider reducing mometasone dose or using an alternative antifungal if prolonged co-administration is necessary. Use with caution.

Ketoconazole
Moderate
Database

Increased systemic exposure to mometasone, potentially leading to Cushing's syndrome or adrenal suppression, especially with prolonged use or high doses.

Monitor for signs of systemic corticosteroid effects. Consider reducing mometasone dose or using an alternative antifungal if prolonged co-administration is necessary. Use with caution.

Cyp3a4 Inducers
Moderate
Database

CYP3A4 inducers may reduce systemic exposure of mometasone by increasing hepatic metabolism, potentially reducing therapeutic efficacy.

Monitor symptom control. May need to increase mometasone dose or switch to alternative therapy.

Source: Kimi deep-research + Cla

Live Vaccines
Moderate
Database

Corticosteroids suppress immune response, potentially reducing vaccine efficacy and increasing risk of infection from live attenuated organisms.

Avoid live vaccines during high-dose corticosteroid therapy. Inactivated vaccines are safe but may have reduced efficacy.

Source: Kimi deep-research + Cla

Nsaids
Moderate
Database

Both corticosteroids and NSAIDs increase GI ulceration and bleeding risk. Additive effect on gastric mucosal damage.

Use PPI or H2-blocker for GI protection if concurrent use necessary. Monitor for GI bleeding.

Source: Kimi deep-research + Cla

Other Corticosteroids
Moderate
Database

Additive systemic corticosteroid effects — increased risk of adrenal suppression, osteoporosis, hyperglycemia, immunosuppression.

Minimize total steroid exposure. If multiple routes needed, use lowest effective doses. Monitor for signs of adrenal suppression.

Source: Kimi deep-research + Cla

Ritonavir
Moderate
Database

Increased systemic exposure to mometasone, potentially leading to Cushing's syndrome or adrenal suppression, especially with prolonged use or high doses.

Monitor for signs of systemic corticosteroid effects. Consider reducing mometasone dose or using an alternative antiretroviral if prolonged co-administration is necessary. Use with caution.

Strong Cyp3a4 Inhibitors
Moderate
Database

CYP3A4 inhibitors may increase systemic exposure of mometasone by reducing hepatic metabolism of the small fraction that is absorbed, potentially increasing risk of systemic corticosteroid effects (adrenal suppression, Cushingoid features).

Monitor for signs of corticosteroid excess. Consider reducing mometasone dose or switching to corticosteroid not metabolized by CYP3A4 (e.g., beclomethasone).

Source: Kimi deep-research + Cla

Clarithromycin
Mild
Database

Potentially increased systemic exposure to mometasone, though less pronounced than with strong inhibitors. Risk of systemic corticosteroid effects may increase with high doses or prolonged use.

Monitor for signs of systemic corticosteroid effects, especially with prolonged use. Generally, dose adjustment is not required for short-term use.

Diltiazem
Mild
Database

Potentially increased systemic exposure to mometasone, though less pronounced than with strong inhibitors. Risk of systemic corticosteroid effects may increase with high doses or prolonged use.

Monitor for signs of systemic corticosteroid effects, especially with prolonged use. Generally, dose adjustment is not required for short-term use.

Erythromycin
Mild
Database

Potentially increased systemic exposure to mometasone, though less pronounced than with strong inhibitors. Risk of systemic corticosteroid effects may increase with high doses or prolonged use.

Monitor for signs of systemic corticosteroid effects, especially with prolonged use. Generally, dose adjustment is not required for short-term use.

Related guidelines

Other Corticosteroid drugs

Ask House about Mometasone

Continue into a citation-backed clinical answer with the drug context already attached.

Sources: KD Tripathi 7e, Katzung, BNF, Nelson·Verified: 2026-05-18 · House clinical team·Cockpit curated: 2026-05-18