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Triamcinolone

    DEA Class; Rx

    Common Brand Names; Triesence, Trivaris Intravitreal

    • Corticosteroids, Ophthalmic

    triamcinolone topical (Rx)

    Brand and Other Names: Kenalog Orabase, Kenalog topical, Pediaderm TA, Triacet, Trianex
    • Classes: Corticosteroids, Topical

    triamcinolone suprachoroidal (Rx)

    Brand and Other Names: Xipere
    • Classes: Corticosteroids, Ophthalmic

    triamcinolone acetonide extended-release injectable suspension (Rx)

    Brand and Other Names: Zilretta
    • Classes: Corticosteroids

    triamcinolone, intranasal (OTC)

    Brand and Other Names: Nasacort Allergy 24HR
    • Classes: Corticosteroids, Intranasal

    triamcinolone acetonide injectable suspension (Rx)

    Brand and Other Names: Kenalog-10, Kenalog-40
    • Classes: Corticosteroids

    Synthetic glucocorticoid with little mineralocorticoid activity; slightly more potent than prednisone
    Used intranasally for allergic rhinitis; used parenterally for inflammation, particularly for articular uses; intravitreal injection used for ophthalmic inflammatory disorders; suprachoroidal injection used for macular edema associated with uveitis
    Topical formulations are of medium or high potency

    Indicated for sympathetic ophthalmia, temporal arteritis, uveitis, and ocular inflammatory conditions unresponsive to ophthalmic corticosteroids

    Indicated for Topical Inflammatory Dermatoses

    Indicated for Oral Inflammatory or Ulcerative Lesions

    Indicated for macular edema associated with uveitis

    Indicated for management of osteoarthritis knee pain, Allergic Rhinitis.

    Treatment of rheumatic or arthritic disorders

    Indicated for treatment of steroid-responsive dermatoses

    Hypersensitivity

    Idiopathic thrombocytopenia purpura

    Systemic fungal infections

    Cerebral malaria

    Underlying fungal, bacterial, or viral infection

    Ophthalmic use

    Hypersensitivity to triamcinolone and other product components

    • Abnormal sensation in eye
    • Anterior chamber cells
    • Anterior chamber flare
    • Cataract
    • Cataract cortical
    • Cataract nuclear
    • Cataract subcapsular
    • Conjunctival hemorrhage
    • Exophthalmos
    • Eye irritation
    • Eye pain
    • Eye pruritus
    • Foreign body sensation in eyes
    • Glaucoma
    • Hypopion
    • Increased intraocular pressure
    • Injection site hemorrhage
    • Lacrimation increased
    • Optic disc vascular disorder
    • Vitreous detachment
    • Vitreous floaters
    • Rare instances of blindness associated with intravitreal or periocular injections
    • Skin atrophy
    • Striae
    • Acneform lesions
    • Pigmentation changes
    • HPA suppression (with higher potency used >2 weeks)
    • Increased intraocular pressure (IOP), nonacute (14%)Eye pain, nonacute (12%)
    • Joint swelling (3%)Contusion (2%)Sinusitis (2%)Cough (2%)Contusions (2%)
    • Flu syndrome [children] (9%)Pharyngitis (5-8%)Headache [children] (6%)Bronchitis [children] (3%)Dyspepsia (3-5%)Tooth disorder [children] (3%)Epistaxis (3-5%)Excoriation [children] (3%)Increased cough (2- 8%)Upper abdominal pain [children] (5%)Diarrhea [children] (3%)Rash [children] (3%)Asthma [children] (3%)Rhinorrhea [children] (2%)

    Prolonged use may produce posterior subcapsular cataracts, glaucoma with possible damage to the optic nerves, and may enhance the establishment of secondary ocular infections due to fungi or viruses

    The use of oral corticosteroids is not recommended in the treatment of optic neuritis and may lead to an increase in the risk of new episodes

    Intraocular pressure may become elevated in some individuals; if steroid therapy is continued for more than 6 weeks, IOP should be monitored

    Corticosteroids should be used cautiously in patients with a history of ocular herpes simplex because of possible corneal perforation; do NOT use in active ocular herpes simplex

    Rate of infectious culture positive endophthalmitis is 0.5%; proper aseptic techniques should always be used when administering triamcinolone acetonide

    In addition, patients should be monitored following the injection to permit early treatment should an infection occur

    Children who are treated with corticosteroids by any route, including systemically administered corticosteroids, may experience a decrease in their growth velocity

    Chronic topical corticosteroid therapy may interfere with growth and development in children

    Use medium to very high potency for <2 weeks to reduce local and systemic side effects

    Use low potency for chronic therapy

    Avoid medium to very high potency on face, folds, and groin because can increase steroid absorption

    Use lower potency for children (ie, increase BSA/kg, therefore increase systemic absorption)

    Prolonged use may result in bacterial or fungal superinferction; discontinue if dermatological infection persists despite antimicrobial therapy

    Discontinue if local sensitization including irritation or redness occurs

    Avoid use of high potency steroids in the face

    Pregnancy Category: D

    Lactation: Distributed in breast milk; caution advised

    triamcinolone topical

    Pregnancy category: C

    Lactation: Not known whether topical corticosteroids are distributed into milk; however, systemic corticosteroids are distributed into milk; use with caution

    Corticosteroid dosage must be individualized and is highly variable depending on the nature and severity of the disease, route of administration, and on patient response.

     

    Prednisolone/Gentamicin

    injectable suspension, intravitreal (as acetonide salt)

    • 4mg/0.1mL

    cream/ointment

    • 0.025%
    • 0.1%
    • 0.5%

    lotion

    • 0.025%
    • 0.1%

    dental paste

    • 0.1%

    aerosol solution

    • 0.0147%

    therapy pack

    • 0.1% (contains cetyl alcohol, methylparaben, propylene glycol)

    kit

    • 0.1% (contains propylene glycol)

    ophthalmic suspension for suprachoroidal injection

    • 40mg/mL single-dose vial

    injectable, powder for reconstitution

    • 32mg/single-dose vial
    • When reconstituted, forms an extended-release suspension

    nasal spray

    • 55mcg/spray
    • Note: Nasacort AQ (Rx) was phased out and replaced by Nasacort Allergy 24HR (OTC) in spring 2014

    injectable suspension

    • 10mg/mL (Kenalog-10; intralesional or intra-articular administration)
    • 40mg/mL (Kenalog-40; IM or intra-articular administration)