Classes
DEA Class; Rx
Common Brand Names; Celestone, Celestone Soluspan, Betaject, Betamethasone IM/PO
- Corticosteroids;
- Immunosuppressives, PHD
betamethasone topical (Rx)
- Classes: Corticosteroids, Topical
Description
Synthetic glucocorticoid with little mineralocorticoid activity
Used as an antiinflammatory or immunosuppressive agent; available systemically (injectable and oral)
Topical formulations are of medium (e.g., betamethasone valerate) or high-to-very high (i.e., betamethasone dipropionate) potency
Indications
Contraindications
Hypersensitivity to betamethasone
Idiopathic thrombocytopenia purpura
Live or live, attenuated vaccines, when immunisuppressive doses of corticosteroids required
Underlying infection present
Hypersensitivity
Ophthalmic use
Adverse Effects
- Blurred vision
- Increased appetite
- Indigestion
- Nervousness
- Itching
- Arthralgia
- Cataracts
- Dizziness
- DM
- Edema
- Erythema (topical)
- Headache
- Seizure
- Skin dryness (topical)
- Vertigo
- Fluid/electrolyte disturbances
- Adrenal suppression
- Psychosis
- Insomnia
- Vertigo
- Pseudotumor cerebri (on withdrawal)
- Acne
- Osteoporosis
- Myopathy
- Delayed wound healing
- Skin atrophy
- Striae
- Allergic dermatitis
- Burning
- Dry skin
- Erythema folliculitis
- Hypertrichosis
- Irritation
- Miliaria
- Vesiculation
- Acneform lesions
- Pigmentation changes
- HPA suppression (with higher potency used >2 wk)
Warnings
Not for IV administration
Use caution in cirrhosis, ocular herpes simplex, HTN, diverticulitis, hypothyroidism, myasthenia gravi, PUD, osteoporosis, ulcerative colitis, psychotic tendencies, untreated systemic infections, renal insufficiency, pregnancy
May cause adrenal suppresion in patients receiving high doses for prolonged periods of time
Prolonged use of corticosteroids may increase incidence of secondary infection
Kaposi sarcoma reported with prolonged treatment of corticosteroids
Thromboembolic disorders
Myopathy associated with high-dose corticosteroids
Seizures reported in patients with history of seizure disorders use caution
Corticosteroids may exacerbate systemic fungal infections
Patients receiving corticosteroids should avoid chickenpox or measles-infected persons if unvaccinated
Restrict the use of corticosteroids in active tuberculosis to cases of fulminating or disseminated tuberculosis when it is used in conjunction with appropriate anti-tuberculous regimen
Monitor closely patients with latent tuberculosis or tuberculin reactivity, if corticosteroid therapy necessary; reactivation of the disease may occur
Killed or inactivated vaccines may be administered; however, the response to such vaccines cannot be predicted
Prolonged corticosteroid use may result in glaucoma and/or cataracts
Intraocular pressure may become elevated in some individuals; monitor if treatment is continued for >6 weeks
Not recommended for treatment of optic neuritis; may lead to an increase in risk of new episodes; should not be used in active ocular herpes simplex
Special consideration should be given to patients at increased risk of osteoporosis (ie, postmenopausal women) before initiating corticosteroid therapy
Chronic topical corticosteroid therapy may interfere with growth and development in children
Prolonged treatment with corticosteroids is associated with Kaposi sarcoma (consider discontinuation of therapy if diagnosed)
Discontinue if contact dermatitis occurs; not for use in patients with decreased skin circulation
Manifestations of Cushing syndrome, hyperglycemia, or glycosuria occur, especially if occlusive dressings are used
Pregnancy and Lactation
Pregnancy Category: C
Lactation: systemically administered corticosteroids enter breast milk and could suppress growth, interfere with endogenous corticosteroid production, or cause other effects; use with caution
Maximum Dosage
Corticosteroid dosage must be individualized and is highly variable depending on the nature and severity of the disease, route of treatment, and on patient response.
50 g/week (Diprolene cream, ointment, gel); 50 ml/week for no longer than 2 weeks (Diprolene lotion).
50 g/week (Diprolene cream, ointment, gel); 50 ml/week for no longer than 2 weeks (Diprolene lotion).
50 g/week (Diprolene cream, ointment, gel); 50 ml/week for no longer than 2 weeks (Diprolene lotion).
Betamethasone dipropionate (augmented) topical products (e.g., Diprolene products) are not recommended.
How supplied
Formulation: 3 mg as betamethasone sodium phosphate and 3 mg as betamethasone acetate
injectable suspension
- 6mg/mL
Betamethasone topical
cream/lotion/ointment
- 0.05%
- 0.1%
gel
- 0.05%
foam
- 0.12% (Luxiq)
spray
- 0.05% (Sernivo)