Dexamethasone
Active ingredient · 11 therapeutic classes
Sold as Neofordex · MAXIDEX · OZURDEX · MAXITROL · LEVODEXA
- Drug class
- Corticosteroids
- Availability
- Prescription only
- Routes
- Oral, Intra-Articular, Intralesional, Intramuscular, Intravenous
- Markets covered
- 4
- Products on record
- 119
- FDA reports (12 mo)
- 16,165
Overview
Dexamethasone is an active pharmaceutical ingredient in the Corticosteroids group (C05AA). The information below is compiled per regulator from the product labels on record, with direct links to the original documents.
Regulatory status by market
| Market | Regulator | Products | Last revision |
|---|---|---|---|
| GB United Kingdom | MHRA | 76 | May 29, 2026 |
| US United States | FDA | 21 | April 24, 2026 |
| CA Canada | Health Canada | 20 | May 19, 2026 |
| EU European Union | EMA | 2 | May 29, 2026 |
GBUnited Kingdom· MHRA
76 products
Uses
Neurology Cerebral oedema caused by brain tumours, neurosurgery, bacterial meningitis, brain abscess. Pulmonary and respiratory diseases Severe acute asthma attack. Dermatology Oral initial treatment of extensive, severe, acute skin diseases that respond to glucocorticoids, such as erythroderma, pemphigus, vulgaris, acute eczema.
Autoimmune disorders/rheumatology Oral initial treatment of autoimmune diseases, such as systemic lupus erythematosus (especially visceral forms). g. rapidly destructive forms and/or with extra-articular manifestations. g. tuberculosis, typhoid) only with concomitant anti-infective therapy.
Oncology Palliative treatment of malignant tumours. Endocrinology Congenital adrenogenital syndrome in adulthood.
USUnited States· FDA
21 products
Uses
INDICATIONS AND USAGE A l l ergic States:
Control of severe or incapacitating a llergic conditions intractable to adequate trials of conventional treatment in asthma, atopic dermatitis, contact dermatitis, drug hypersensitivity reactions, perennial or seasonal allergic rhinitis, and serum sickness.
Dermatologic Diseases:
Bul l ous dermatitis herpetiformis, exfoliative erythroderma, mycosis fungoides, pemphigus, and severe erythema multiforme (Stevens-Johnson syndrome).
Endocrine Disorders:
Primary or secondary adrenocortical insufficiency (hydrocortisone or cortisone is the drug of choice; may be used in conjunction with synthetic mineralocorticoid analogs where applicable; in infancy mineralocorticoid supplementation is of particular importance), congenital adrenal hyperplasia, hypercalcemia associated with cancer, and nonsuppurative thyroiditis.
CACanada· Health Canada
20 products
Uses
MAXIDEX® (dexamethasone ophthalmic ointment, USP and dexamethasone ophthalmic suspension, BP) is indicated for: • Steroid responsive inflammatory conditions of the palpebral and bulbar conjunctiva, cornea and anterior segment of the globe, such as allergic conjunctivitis, acne rosacea, superficial punctate keratitis, iritis, cyclitis, and selected infective conjunctivitis when the inherit hazard of steroid use is acceptable to obtain an advisable diminution in edema and inflammation.
• Corneal injury from chemical, radiation or thermal burns, or penetration of foreign bodies. 1 Pediatrics Pediatrics (< 18 years of age): The safety and efficacy of MAXIDEX in children have not been established. 2 Geriatrics Geriatrics (> 60 years of age): No overall differences in safety or effectiveness have been observed between elderly and younger patients.
EUEuropean Union· EMA
2 products
Uses
1) • inflammation of the posterior segment of the eye presenting as non-infectious uveitis
How to take
Drug interactions
Known interactions involving Dexamethasone. Select one for details. This list is informational and not a complete interaction checker.
Showing 240 of 600. Type above to find a specific drug.
Interaction data compiled from DDInter (academic, CC-BY). Severity classification only - this is not a complete interaction checker and not medical advice.
Sources & citations
- [1]MHRA (UK) · PL529140002 · revised January 6, 2023
- [2]FDA DailyMed · 01cfaa3e-5e30-18… · revised October 29, 2025 [PDF]
- [3]Health Canada (DPD) · 00042560 · revised March 22, 2025
- [4]European Medicines Agency · EMEA/H/C/001140 · revised May 29, 2026
- [5]OpenFDA adverse-event reports (US), 12 months ending June 4, 2026.
Information on this page is compiled from public regulatory records. Drugvu is not affiliated with any regulator or pharmaceutical manufacturer. This is not medical advice. Always consult a qualified healthcare professional.