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TRIDERM

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Overview

What is TRIDERM?

The topical corticosteroids constitute a class of primarily synthetic steroids used as anti-inflammatory and antipruritic agents. Triamcinolone acetonide is a member of this class. Triamcinolone acetonide is chemically pregna-1,4-diene-3,20-dione, 9-fluoro-11,21-dihydroxy-16,17-[(1-methylethylidene)bis-(oxy)]-(11β, 16α)- with the empirical formula C H FO and molecular weight 434.50. Its structural formula is:

Each gram of Triderm (Triamcinolone Acetonide Cream USP), 0.025% contains 0.25 mg triamcinolone acetonide USP in a cream base consisting of purified water, emulsifying wax, mineral oil, propylene glycol, sorbitol solution, cetyl palmitate, sorbic acid, and potassium sorbate.



What does TRIDERM look like?



What are the available doses of TRIDERM?

Sorry No records found.

What should I talk to my health care provider before I take TRIDERM?

Sorry No records found

How should I use TRIDERM?

Topical corticosteroids are indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses.

Apply to the affected area as a thin film from two to four times daily for the 0.025% strength and two or three times daily for the 0.1% and 0.5% strength depending on the severity of the condition. Occlusive dressings may be used for the management of psoriasis or recalcitrant conditions. If an infection develops, the use of occlusive dressings should be discontinued and appropriate antimicrobial therapy instituted.


What interacts with TRIDERM?

Sorry No Records found


What are the warnings of TRIDERM?

Sorry No Records found


What are the precautions of TRIDERM?

Sorry No Records found


What are the side effects of TRIDERM?

Sorry No records found


What should I look out for while using TRIDERM?

Topical corticosteroids are contraindicated in those patients with a history of hypersensitivity to any of the components of the preparation.


What might happen if I take too much TRIDERM?

Topically applied corticosteroids can be absorbed in sufficient amounts to produce systemic effects. (See )


How should I store and handle TRIDERM?

Store at controlled room temperature 20° to 25°C (68° to 77°F) [see USP].Triderm (Triamcinolone Acetonide Cream USP), 0.025% is supplied in:15 grams tube NDC 0316-0165-1585.2 grams tube NDC 0316-0165-85454 grams jar NDC 0316-0165-16Triderm (Triamcinolone Acetonide Cream USP), 0.1% is supplied in: 28.4 grams tube NDC 0316-0170-01 85.2 grams tube NDC 0316-0170-03Triderm (Triamcinolone Acetonide Cream USP), 0.5% is supplied in:15 grams tube NDC 0316-0175-15454 grams jar NDC 0316-0175-16Triderm (Triamcinolone Acetonide Cream USP), 0.025% is supplied in:15 grams tube NDC 0316-0165-1585.2 grams tube NDC 0316-0165-85454 grams jar NDC 0316-0165-16Triderm (Triamcinolone Acetonide Cream USP), 0.1% is supplied in: 28.4 grams tube NDC 0316-0170-01 85.2 grams tube NDC 0316-0170-03Triderm (Triamcinolone Acetonide Cream USP), 0.5% is supplied in:15 grams tube NDC 0316-0175-15454 grams jar NDC 0316-0175-16Triderm (Triamcinolone Acetonide Cream USP), 0.025% is supplied in:15 grams tube NDC 0316-0165-1585.2 grams tube NDC 0316-0165-85454 grams jar NDC 0316-0165-16Triderm (Triamcinolone Acetonide Cream USP), 0.1% is supplied in: 28.4 grams tube NDC 0316-0170-01 85.2 grams tube NDC 0316-0170-03Triderm (Triamcinolone Acetonide Cream USP), 0.5% is supplied in:15 grams tube NDC 0316-0175-15454 grams jar NDC 0316-0175-16Triderm (Triamcinolone Acetonide Cream USP), 0.025% is supplied in:15 grams tube NDC 0316-0165-1585.2 grams tube NDC 0316-0165-85454 grams jar NDC 0316-0165-16Triderm (Triamcinolone Acetonide Cream USP), 0.1% is supplied in: 28.4 grams tube NDC 0316-0170-01 85.2 grams tube NDC 0316-0170-03Triderm (Triamcinolone Acetonide Cream USP), 0.5% is supplied in:15 grams tube NDC 0316-0175-15454 grams jar NDC 0316-0175-16Triderm (Triamcinolone Acetonide Cream USP), 0.025% is supplied in:15 grams tube NDC 0316-0165-1585.2 grams tube NDC 0316-0165-85454 grams jar NDC 0316-0165-16Triderm (Triamcinolone Acetonide Cream USP), 0.1% is supplied in: 28.4 grams tube NDC 0316-0170-01 85.2 grams tube NDC 0316-0170-03Triderm (Triamcinolone Acetonide Cream USP), 0.5% is supplied in:15 grams tube NDC 0316-0175-15454 grams jar NDC 0316-0175-16Triderm (Triamcinolone Acetonide Cream USP), 0.025% is supplied in:15 grams tube NDC 0316-0165-1585.2 grams tube NDC 0316-0165-85454 grams jar NDC 0316-0165-16Triderm (Triamcinolone Acetonide Cream USP), 0.1% is supplied in: 28.4 grams tube NDC 0316-0170-01 85.2 grams tube NDC 0316-0170-03Triderm (Triamcinolone Acetonide Cream USP), 0.5% is supplied in:15 grams tube NDC 0316-0175-15454 grams jar NDC 0316-0175-16Triderm (Triamcinolone Acetonide Cream USP), 0.025% is supplied in:15 grams tube NDC 0316-0165-1585.2 grams tube NDC 0316-0165-85454 grams jar NDC 0316-0165-16Triderm (Triamcinolone Acetonide Cream USP), 0.1% is supplied in: 28.4 grams tube NDC 0316-0170-01 85.2 grams tube NDC 0316-0170-03Triderm (Triamcinolone Acetonide Cream USP), 0.5% is supplied in:15 grams tube NDC 0316-0175-15454 grams jar NDC 0316-0175-16Triderm (Triamcinolone Acetonide Cream USP), 0.025% is supplied in:15 grams tube NDC 0316-0165-1585.2 grams tube NDC 0316-0165-85454 grams jar NDC 0316-0165-16Triderm (Triamcinolone Acetonide Cream USP), 0.1% is supplied in: 28.4 grams tube NDC 0316-0170-01 85.2 grams tube NDC 0316-0170-03Triderm (Triamcinolone Acetonide Cream USP), 0.5% is supplied in:15 grams tube NDC 0316-0175-15454 grams jar NDC 0316-0175-16Triderm (Triamcinolone Acetonide Cream USP), 0.025% is supplied in:15 grams tube NDC 0316-0165-1585.2 grams tube NDC 0316-0165-85454 grams jar NDC 0316-0165-16Triderm (Triamcinolone Acetonide Cream USP), 0.1% is supplied in: 28.4 grams tube NDC 0316-0170-01 85.2 grams tube NDC 0316-0170-03Triderm (Triamcinolone Acetonide Cream USP), 0.5% is supplied in:15 grams tube NDC 0316-0175-15454 grams jar NDC 0316-0175-16


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Clinical Information

Chemical Structure

No Image found
Clinical Pharmacology

Topical corticosteroids share anti-inflammatory, antipruritic and vasoconstrictive actions. The mechanism of anti-inflammatory activity of the topical corticosteroids is unclear. Various laboratory methods, including vasoconstrictor assays, are used to compare and predict potencies and/or clinical efficacies of the topical corticosteroids. There is some evidence to suggest that a recognizable correlation exists between vasoconstrictor potency and therapeutic efficacy in man.

DOSAGE AND ADMINISTRATION

Non-Clinical Toxicology
Topical corticosteroids are contraindicated in those patients with a history of hypersensitivity to any of the components of the preparation.

The concomitant use of oxybutynin with other anticholinergic drugs or with other agents which produce dry mouth, constipation, somnolence (drowsiness), and/or other anticholinergic-like effects may increase the frequency and/or severity of such effects.

Anticholinergic agents may potentially alter the absorption of some concomitantly administered drugs due to anticholinergic effects on gastrointestinal motility. This may be of concern for drugs with a narrow therapeutic index.

Mean oxybutynin chloride plasma concentrations were approximately 3 to 4 fold higher when oxybutynin chloride was administered with ketoconazole, a potent CYP3A4 inhibitor.

Other inhibitors of the cytochrome P450 3A4 enzyme system, such as antimycotic agents (e.g., itraconazole and miconazole) or macrolide antibiotics (e.g., erythromycin and clarithromycin), may alter oxybutynin mean pharmacokinetic parameters (i.e., C and AUC). The clinical relevance of such potential interactions is not known. Caution should be used when such drugs are co-administered.

General

PRECAUTIONS-Pediatric use

The following local adverse reactions are reported infrequently with topical corticosteroids, but may occur more frequently with the use of occlusive dressings. These reactions are listed in an approximate decreasing order of occurrence: burning, itching, irritation, dryness, folliculitis, hypertrichosis, acneiform eruptions, hypopigmentation, perioral dermatitis, allergic contact dermatitis, maceration of the skin, secondary infection, skin atrophy, striae, miliaria.

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Reference

This information is obtained from the National Institute of Health's Standard Packaging Label drug database.
"https://dailymed.nlm.nih.gov/dailymed/"

While we update our database periodically, we cannot guarantee it is always updated to the latest version.

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Professional

Clonazepam Description Each single-scored tablet, for oral administration, contains 0.5 mg, 1 mg, or 2 mg Clonazepam, USP, a benzodiazepine. Each tablet also contains corn starch, lactose monohydrate, magnesium stearate, microcrystalline cellulose, and povidone. Clonazepam tablets USP 0.5 mg contain Yellow D&C No. 10 Aluminum Lake. Clonazepam tablets USP 1 mg contain Yellow D&C No. 10 Aluminum Lake, as well as FD&C Blue No. 1 Aluminum Lake. Chemically, Clonazepam, USP is 5-(o-chlorophenyl)-1,3-dihydro-7-nitro-2H-1,4-benzodiazepin-2-one. It is a light yellow crystalline powder. It has the following structural formula: C15H10ClN3O3 M.W. 315.72
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Tips

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Interactions

Interactions

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