triamcinolone (topical)_ drug information
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28/01/13 Triamcinolone (topical): Drug information
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Triamcinolone (topical): Drug information
Copyright 1978-2013 Lexicomp, Inc. All rights reserved.
(For additional information see "Triamcinolone (topical): Patient drug information" and see "Triamcinolone(topical): Pediatric drug information")
For abbreviations and symbols that may be used in Lexicomp (show table)
Brand Names: U.S. Kenalog®; Oralone®; Pediaderm™ TA; Trianex™; Triderm®; Zytopic™
Brand Names: Canada Kenalog®; Oracort; Triaderm
Pharmacologic Category Corticosteroid, Topical
Dosing: Adult
Dermatoses (steroid-responsive, including contact/atopic dermatitis): Topical:
Cream, Ointment:
0.025% or 0.05%: Apply thin film to affected areas 2-4 times/day
0.1% or 0.5%: Apply thin film to affected areas 2-3 times/day
Spray: Apply to affected area 3-4 times/day
Oral inflammatory lesions/ulcers: Oral topical: Press a small dab (about 1/4 inch) to the lesion until a thin
film develops; a larger quantity may be required for coverage of some lesions. For optimal results, use only
enough to coat the lesion with a thin film; do not rub in.
Dosing: Geriatric Refer to adult dosing.
Dosage Forms: U.S. Excipient information presented when available (limited, particularly for generics);
consult specific product labeling.
Aerosol, spray, topical, as acetonide:
Kenalog®: 0.2 mg/2-second spray (63 g, 100 g) [contains dehydrated ethanol 10.3%]
Cream, topical, as acetonide: 0.025% (15 g, 80 g, 454 g); 0.1% (15 g, 30 g, 80 g, 454 g); 0.5% (15 g)
Triderm®: 0.1% (30 g, 85 g)
Cream, topical, as acetonide [kit]:
Pediaderm™ TA: 0.1% (30 g) [packaged with protective emollient]
Zytopic™: 0.1% (85 g) [packaged with cleanser and moisturizer]
Lotion, topical, as acetonide: 0.025% (60 mL); 0.1% (60 mL); 0.1%
Ointment, topical, as acetonide: 0.025% (15 g, 80 g, 454 g); 0.05% (430 g); 0.1% (15 g, 80 g, 454 g); 0.5% (15
g)
Trianex™: 0.05% (17 g, 85 g)
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28/01/13 Triamcinolone (topical): Drug information
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Paste, oral topical, as acetonide: 0.1% (5 g)
Oralone®: 0.1% (5 g)
Generic Equivalent Available: U.S. Yes: Excludes spray
Administration
Oral topical: Apply small dab to lesion until a thin film develops; do not rub in. Apply at bedtime or after meals if
applications are needed throughout the day.
Topical:
Ointment: Apply a thin film sparingly. Do not use on open skin or wounds. Do not occlude area unless
directed; if using occluding dressing, monitor for infection.
Spray: Avoid eyes and do not inhale if spraying near face. Occlusive dressing may be used if instructed;
monitor for infection.
Use
Oral topical: Adjunctive treatment and temporary relief of symptoms associated with oral inflammatory lesions
and ulcerative lesions resulting from trauma
Topical: Inflammatory dermatoses responsive to steroids
Medication Safety Issues
Sound-alike/look-alike issues:
Kenalog® may be confused with Ketalar®
Other safety concerns:
TAC (occasional abbreviation for triamcinolone) is an error-prone abbreviation (mistaken as tetracaine-
adrenaline-cocaine)
Adverse Reactions Significant Frequency not defined.
Dermatologic: Acneiform eruptions, allergic contact dermatitis, dryness, folliculitis, hypertrichosis,
hypopigmentation, miliaria, perioral dermatitis, pruritus, skin atrophy, skin infection (secondary), skin
maceration, striae
Endocrine: HPA axis suppression; metabolic effects (hyperglycemia, hypokalemia)
Local: Burning, irritation
Contraindications Hypersensitivity to triamcinolone or any component of the formulation; fungal, viral, or
bacterial infections of the mouth or throat (oral topical formulation)
Warnings/Precautions
Concerns related to adverse effects:
• Adrenal suppression: May cause hypercorticism or suppression of hypothalamic-pituitary-adrenal (HPA)
axis, particularly in younger children or in patients receiving high doses for prolonged periods. HPA
axis suppression may lead to adrenal crisis.
• Immunosuppression: Prolonged use may result in fungal or bacterial superinfection; discontinue if
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28/01/13 Triamcinolone (topical): Drug information
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(For additional information: Launch Lexi-Interact™ Drug Interactions Program)
dermatological infection persists despite appropriate antimicrobial therapy.
• Sensitization: Topical use has been associated with local sensitization (redness, irritation); discontinue if
sensitization is noted.
• Systemic effects: Topical corticosteroids may be absorbed percutaneously. Absorption may cause
manifestations of Cushing's syndrome, hyperglycemia, or glycosuria. Absorption is increased by the
use of occlusive dressings, application to denuded skin, or application to large surface areas.
Special populations:
• Elderly: Because of the risk of adverse effects associated with systemic absorption, topical
corticosteroids should be used cautiously in the elderly in the smallest possible effective dose for the
shortest duration.
• Pediatrics: Children may absorb proportionally larger amounts after topical application and may be more
prone to systemic effects. HPA axis suppression, intracranial hypertension, and Cushing's syndrome
have been reported in children receiving topical corticosteroids. Prolonged use may affect growth
velocity; growth should be routinely monitored in pediatric patients.
Other warnings/precautions:
• Appropriate use: Do not use occlusive dressings on weeping or exudative lesions and general caution with
occlusive dressings should be observed; discontinue if skin irritation or contact dermatitis should
occur; do not use in patients with decreased skin circulation.
• High-potency products: Avoid the use of high-potency steroids on the face.
• Oral cavity application: When used as a topical agent in the oral cavity, if significant regeneration or repair
of oral tissues has not occurred in seven days, re-evaluation of the etiology of the oral lesion is
advised.
Metabolism/Transport Effects None known.
Drug Interactions
Aldesleukin: Corticosteroids may diminish the antineoplastic effect of Aldesleukin. Risk X: Avoid combination
Corticorelin: Corticosteroids may diminish the therapeutic effect of Corticorelin. Specifically, the plasma ACTH
response to corticorelin may be blunted by recent or current corticosteroid therapy. Risk C: Monitor therapy
Deferasirox: Corticosteroids may enhance the adverse/toxic effect of Deferasirox. Specifically, the risk for GI
ulceration/irritation or GI bleeding may be increased. Risk C: Monitor therapy
Hyaluronidase: Corticosteroids may diminish the therapeutic effect of Hyaluronidase. Management: Patients
receiving corticosteroids (particularly at larger doses) may not experience the desired clinical response to
standard doses of hyaluronidase. Larger doses of hyaluronidase may be required. Risk D: Consider therapy
modification
Telaprevir: Corticosteroids may decrease the serum concentration of Telaprevir. Telaprevir may increase the
serum concentration of Corticosteroids. Management: Concurrent use of telaprevir and systemic
corticosteroids is not recommended. When possible, consider alternatives. If used together, employ extra
caution and monitor closely for excessive corticosteroid effects and diminished telaprevir effects. Risk D:
Consider therapy modification
Pregnancy Risk Factor C (show table)
Pregnancy Implications Corticosteroids were found to be teratogenic following topical application in
animal reproduction studies. In general, the use of topical corticosteroids during pregnancy is not considered to
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28/01/13 Triamcinolone (topical): Drug information
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have significant risk, however, intrauterine growth retardation in the infant has been reported (rare). The use of
large amounts or for prolonged periods of time should be avoided.
Lactation Excretion in breast milk unknown/use caution
Breast-Feeding Considerations Corticosteroids are excreted in human milk; information specific to
triamcinolone has not been located. The amount of triamcinolone absorbed systemically following topical
administration is variable. Hypertension in the nursing infant has been reported following corticosteroid ointment
applied to the nipples. Use with caution.
Pricing: U.S. (www.drugstore.com)
Aerosol solution (Kenalog)
(63): $175.99
Cream (Triamcinolone Acetonide)
0.025% (15): $15.99
0.03% (80): $17.99
0.1% (15): $14.99
0.1% (30): $18.99
0.1% (80): $19.99
0.1% (453.6): $40.99
0.5% (15): $19.99
Lotion (Triamcinolone Acetonide)
0.025% (60): $40.99
0.1% (60): $43.99
Ointment (Triamcinolone Acetonide)
0.03% (80): $17.99
0.1% (15): $14.99
0.1% (80): $29.99
0.1% (454): $31.99
0.5% (15): $20.99
Paste (Triamcinolone Acetonide)
0.1% (5): $65.99
International Brand Names Aftab (DE); Ahbina (KP); Aristo (HK); Aristocort A (MY, TH); Centocort
(TH); Cortiflex (PE); Delphi Creme (BE, NL); Delphicort (AT, DE); Dermacort (HK, MY); Facort (TH); Ftoracort(EE); Gemicort (KP); Generlog (TH); Glytop (AR); Invert Plaster (KP); Kanolone (MY); Kena-Lite (TH); Kenacort(PH, VE); Kenacort A (NL); Kenacort A in Orabase (CH); Kenacort E (PE); Kenacort T (FI, SE); Kenacort-A(BH, EG, ID, KE, TW, TZ, UG); Kenacort-A in Orabase (NL); Kenalog (CL, DK, PK); Kenalog Gel (CL); Kenalogin Orabase (ID, ZA); Keno (SG); Ketricin (ID); Laver (TH); Ledercort (AR, IN, PK); Ledermix (NO); Manolone(TH); Metoral (MY, TH); Nincort (CL, TW); Oracort (NZ); Oramedy (HK, KP, SG); Orrepaste (MY, SG); Sinocort(ID); Tess (IN); Tramsone (SG); Tricin (PH); Tricort (FI, PH); Tricortone (AU); Volon A Antibiotikafrei (AT, DE)
Mechanism of Action Decreases inflammation by suppression of migration of polymorphonuclear
leukocytes and reversal of increased capillary permeability; suppresses the immune system by reducing activity
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28/01/13 Triamcinolone (topical): Drug information
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and volume of the lymphatic system
Pharmacodynamics/Kinetics
Absorption: Topical corticosteroids are absorbed percutaneously. The extent is dependent on several factors,
including epidermal integrity (intact vs abraded skin), formulation, and the use of occlusive dressings.
Half-life elimination: Biologic: 18-36 hours
Excretion: Urine (~40%); feces (~60%)
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REFERENCES
1. American Academy of Pediatrics Committee on Drugs: “Transfer of Drugs and Other Chemicals Into Human Milk,”
Pediatrics, 2001, 108(3):776-89. [PubMed 11533352]
2. Pradat P, Robert-Gnansia E, Di Tanna GL, et al, “First Trimester Exposure to Corticosteroids and Oral Clefts,” Birth Defects
Res A Clin Mol Teratol, 2003, 67(12):968-70. [PubMed 14745915]
3. Reed, BR, “Dermatologic Drugs, Pregnancy, and Lactation. A Conservative Guide,” Arch Dermatol, 1997, 133(7):894-8.
[PubMed 9236528]
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