Triamcinolone target pharmacy

Investigational The risk or severity of adverse effects can be increased when Triamcinolone is combined with Pyridostigmine. Approved The serum concentration of Triamcinolone can be increased when it is combined with Quinestrol.

Approved Triamcinolone may increase the hypokalemic activities of Quinethazone. Approved The therapeutic efficacy of Rabies virus inactivated antigen, A can be decreased when used in combination with Triamcinolone. Approved The metabolism of Triamcinolone can be decreased when combined with Ranolazine.

Approved, Investigational Rapacuronium may increase the adverse neuromuscular activities of Triamcinolone. Withdrawn The therapeutic efficacy of Repaglinide can be decreased when used in combination with Triamcinolone.

Approved, Investigational The risk or severity of adverse effects can be increased when Resveratrol is combined with Triamcinolone.

Approved, Experimental, Investigational The metabolism of Triamcinolone can be increased when combined with Rifabutin. Approved The metabolism of Triamcinolone can be increased when combined with Rifampicin. Approved The metabolism of Triamcinolone can be increased when combined with Rifapentine. Approved The risk or severity of adverse effects can be increased when Ritonavir is combined with Triamcinolone.

Approved, Investigational The risk or severity of adverse effects can be increased when Triamcinolone is combined with Rivastigmine.

Approved, Investigational The risk or severity of adverse effects can be increased when Rofecoxib is combined with Triamcinolone. Investigational, Withdrawn Roflumilast may increase the immunosuppressive activities of Triamcinolone. Approved The therapeutic efficacy of Rosiglitazone can be decreased when used in combination with Triamcinolone. Approved, Investigational The risk or severity of adverse effects can be increased when Triamcinolone is combined with Rosoxacin.

Approved, Investigational Rufloxacin The risk or severity of adverse effects can be increased when Triamcinolone is combined with Rufloxacin. Experimental The risk or severity of adverse effects can be increased when Salicylamide is combined with Triamcinolone. Approved The risk or severity of adverse effects can be increased when Salicylic acid is combined with Triamcinolone. Approved, Vet Approved The risk or severity of adverse effects can be increased when Salsalate is combined with Triamcinolone.

Approved The metabolism of Triamcinolone can be decreased when combined with Saquinavir. Approved, Investigational The therapeutic efficacy of Saxagliptin can be decreased when used in combination with Triamcinolone. Approved The serum concentration of Triamcinolone can be increased when it is combined with Secoisolariciresinol. Investigational The risk or severity of adverse effects can be increased when Semapimod is combined with Triamcinolone. Investigational The risk or severity of adverse effects can be increased when Seratrodast is combined with Triamcinolone.

Approved The risk or severity of adverse effects can be increased when Serrapeptase is combined with Triamcinolone. Investigational The metabolism of Triamcinolone can be decreased when combined with Sildenafil. Approved, Investigational The serum concentration of Triamcinolone can be decreased when it is combined with Siltuximab. Approved The serum concentration of Triamcinolone can be increased when it is combined with Simeprevir. Approved The therapeutic efficacy of Sipuleucel-T can be decreased when used in combination with Triamcinolone.

Approved Sitafloxacin The risk or severity of adverse effects can be increased when Triamcinolone is combined with Sitafloxacin. Experimental, Investigational The therapeutic efficacy of Sitagliptin can be decreased when used in combination with Triamcinolone. Approved, Investigational The therapeutic efficacy of Sotagliflozin can be decreased when used in combination with Triamcinolone.

Investigational The risk or severity of adverse effects can be increased when Triamcinolone is combined with Sparfloxacin. Approved, Investigational The risk or severity of adverse effects can be increased when SRT is combined with Triamcinolone.

Investigational The serum concentration of Triamcinolone can be decreased when it is combined with St. Investigational, Nutraceutical Triamcinolone may increase the fluid retaining activities of Stanozolol. Approved, Vet Approved The serum concentration of Triamcinolone can be increased when it is combined with Stiripentol. Approved The risk or severity of adverse effects can be increased when Sulfasalazine is combined with Triamcinolone. Approved The metabolism of Triamcinolone can be decreased when combined with Sulfisoxazole.

Approved, Vet Approved The risk or severity of adverse effects can be increased when Sulindac is combined with Triamcinolone. Approved The therapeutic efficacy of Sulodexide can be decreased when used in combination with Triamcinolone. Approved, Investigational The risk or severity of adverse effects can be increased when Suprofen is combined with Triamcinolone. Approved, Withdrawn Suxibuzone The risk or severity of adverse effects can be increased when Suxibuzone is combined with Triamcinolone.

Experimental The serum concentration of Triamcinolone can be increased when it is combined with Synthetic Conjugated Estrogens, A. Approved The serum concentration of Triamcinolone can be increased when it is combined with Synthetic Conjugated Estrogens, B. Approved The risk or severity of adverse effects can be increased when Triamcinolone is combined with Tacrine. Investigational, Withdrawn The risk or severity of adverse effects can be increased when Tacrolimus is combined with Triamcinolone.

Approved, Investigational The risk or severity of adverse effects can be increased when Tarenflurbil is combined with Triamcinolone. Investigational The serum concentration of Telaprevir can be decreased when it is combined with Triamcinolone. Approved, Withdrawn The metabolism of Triamcinolone can be decreased when combined with Telithromycin. Approved The risk or severity of adverse effects can be increased when Triamcinolone is combined with Temafloxacin. Withdrawn Tenidap The risk or severity of adverse effects can be increased when Tenidap is combined with Triamcinolone.

Experimental The risk or severity of adverse effects can be increased when Tenoxicam is combined with Triamcinolone. Approved Tepoxalin The risk or severity of adverse effects can be increased when Tepoxalin is combined with Triamcinolone.

Vet Approved The risk or severity of adverse effects can be increased when Teriflunomide is combined with Triamcinolone. Approved Triamcinolone may increase the fluid retaining activities of Testosterone. Approved, Investigational The risk or severity of adverse effects can be increased when Tiaprofenic acid is combined with Triamcinolone. Approved The serum concentration of Triamcinolone can be increased when it is combined with Tibolone. Approved, Investigational The metabolism of Triamcinolone can be decreased when combined with Ticlopidine.

Approved The risk or severity of adverse effects can be increased when Tinoridine is combined with Triamcinolone. Investigational The serum concentration of Triamcinolone can be decreased when it is combined with Tocilizumab. Approved Triamcinolone may increase the immunosuppressive activities of Tofacitinib. Approved, Investigational The therapeutic efficacy of Tolazamide can be decreased when used in combination with Triamcinolone. Approved The therapeutic efficacy of Tolbutamide can be decreased when used in combination with Triamcinolone.

Approved The risk or severity of adverse effects can be increased when Tolfenamic Acid is combined with Triamcinolone. Approved The risk or severity of adverse effects can be increased when Tolmetin is combined with Triamcinolone.

Approved Triamcinolone may increase the hypokalemic activities of Torasemide. Approved The risk or severity of adverse effects can be increased when Tranilast is combined with Triamcinolone. Approved, Investigational Trastuzumab may increase the neutropenic activities of Triamcinolone. Approved, Investigational Tribenoside The risk or severity of adverse effects can be increased when Tribenoside is combined with Triamcinolone.

Nursing Mothers It is not known whether oral application of corticosteroids could result in sufficient systemic absorption to produce detectable quantities in breast milk. Caution should be exercised when corticosteroid-containing dental pastes are prescribed for a nursing woman. Pediatric Use The safety and efficacy of triamcinolone acetonide dental paste in children is unknown.

Pediatric patients may demonstrate greater susceptibility to topical corticosteroid-induced HPA axis suppression and Cushing's Syndrome than mature patients because of a larger skin surface area to body weight ratio. Administration of corticosteroid-containing dental pastes to children should be limited to the least amount compatible with an effective therapeutic regimen.

Chronic corticosteroid therapy may interfere with the growth and development of children. Geriatric Use Clinical studies of triamcinolone acetonide dental paste did not include sufficient numbers of subjects age 65 and older to determine whether they respond differently from younger subjects. Other reported clinical experience has not identified differences in responses between the elderly and younger patients. Nursing Mothers It is not known whether topical administration of corticosteroids could result in sufficient systemic absorption to produce detectable quantities in breast milk.

Systemically administered corticosteroids are secreted into breast milk in quantities not likely to have a deleterious effect on the infant. Nevertheless, caution should be exercised when topical corticosteroids are administered to a nursing woman. Pediatric Use Pediatric patients may demonstrate greater susceptibility to topical corticosteroid-induced H PA axis suppression and Cushing's syndrome than mature patients because of a larger skin surface area to body weight ratio.

Administration of corticosteroid-containing dental pastes to children should be limited to the least amount compatible with an effective therapeutic regimen. Chronic corticosteroid therapy may interfere with the growth and development of children. Other reported clinical experience has not identified differences in responses between the elderly and younger patients.

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. Once absorbed through the skin, topical corticosteroids are handled through pharmacokinetic pathways similar to systemically administered corticosteroids.

Corticosteroids are bound to plasma proteins in varying degrees. Corticosteroids are metabolized primarily in the liver and are then excreted by the kidneys. Some of the topical corticosteroids and their metabolites are also excreted into the bile. Triamcinolone acetonide cream 0. Topical corticosteroids are contraindicated in those patients with a history of hypersensitivity to any of the components of the preparation.

Systemic absorption of topical corticosteroids has produced reversible hypo-thalamic-pituitary-adrenal HPA axis suppression, manifestations of Cushing's syndrome, hyperglycemia, and glycosuria in some patients. Conditions which augment systemic absorption include the application of the more potent steroids, use over large surface areas, prolonged use, and the addition of occlusive dressings.

If HPA axis suppression or elevation of the body temperature occurs, an attempt should be made to withdraw the drug, to reduce the frequencies of application, substitute a less potent steroid, or use a sequential approach when utilizing the occlusive technique.

Recovery of HPA axis function and thermal homeostasis are generally prompt and complete upon discontinuation of the drug. Triamcinolone cream will face hair go away Triamcinolone injection south africa. Triamcinolone acetonide acetate and miconazole nitrate and neomycin triamcinolone cream walgreens cream.

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