| Term 
 | Definition 
 
        | acne treatment -synthetic retinoid administered orally
 USE: reserved only for sever cystic acne not responding to standard therapy, reduces size and function of sebaceous glands
 SE: hypervitaminosis A, dryness and itching of skin and mucous membranes, headache, corneal opacities, alopecia, muscle/joint pains, TERATOGENIC
 TOX: suspend drug at least 1 month before discontinuing contraceptives, start contraceptives at least 1 month before beginning this drug and for at least 1 menstrual cycle following drug cessation
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        | Term 
 | Definition 
 
        | acne treatment MOA: naphtoic acid derivative resembling retinoic acid in structure and effects
 -unlike RA, photochemically stable and shows little decrease in efficacy in combo with benzoyl peroxide
 -applied topically
 -less irritant than tretoin
 USE: pts with mild to moderate acne vulgaris
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        | Term 
 
        | Retinoic acid (Tretinoin) |  | Definition 
 
        | acne treatment -acid form of Vit A
 MOA: decreases cohesion between epidermal cells and increases their turnover -> transformation of closed comedones into open ones -> expulsion; stabilizes lysosomes, increases RNA polymerase activity, PGE2, cAMP levels, incorporation of thymidine into DNA
 USE: topically for acne vulgaris (remains mostly in epidermis)
 PK: during 1st 4-6 weeks make seem to make acne worse, but after 8-12 weeks condition will improve
 TOX: slight erythema with mild peeling, skin irritation; must avoid sun because drug may increase UV light potential to produce skin tumors
 -apply to dry skin only
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        | Term 
 | Definition 
 
        | sunshade MOA: contains opaque compounds known to reflect UV light, little used
 USE:  infants-6 months to 2 yrs
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        | Term 
 | Definition 
 
        | sunscreen MOA: contain chemical compounds to absorb UV light responsible for most erythema and tannning sun exposure
 -for children greater than two years old, adults
 -half-life of about 2 yrs
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        | Term 
 
        | Psoralens (Trioxsalen, Methoxsalen) |  | Definition 
 
        | repigmentation MOA: photoactivated by long-wavelength UV light -> intercalate with DNA
 USE: repigment depigmented macules of vitiligo
 TOX: long-term use -> cataracts and skin cancer
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        | Term 
 
        | Hydroquinone (reversible), Monobenzone (irreversible) |  | Definition 
 
        | depigmentation H-MOA: inhibt tyrosinase -> block synthesis of melanin
 M-MOA: toxic to melanocytes
 USE: reduce skin hyperpigmentation
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        | Term 
 | Definition 
 
        | antiectoparasiticide USE: pediculosis capitis, corporis, pubis, scabies
 -lack of systemic side effects makes it a safe alternative scabicide in infants and pregnancy
 SE: skin staining, unpleasant odor
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        | Term 
 | Definition 
 
        | antiectoparasiticide USE: pediculosis capitis, corporis, pubis, scabies
 PK: shampoo or lotion prep
 TOX: neurotoxicity and nephrotoxicity (some systemic absorption may occur after cutaneous use), concentrated in fatty tissue and brain
 -not used during pregnancy, infants, seizure-prone individuals
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        | Term 
 | Definition 
 
        | antiviral USE: recurrent orolabial HSV infections in immunocompromised pts
 -cream applied at first signs of infection, reapplied every 2h for 4d reduces time of viral shedding and decreases healing time by one day
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        | Term 
 | Definition 
 
        | antiviral USE: primary cutaneous HS and limited mucocutaneous HS in immunocompromised pts, decreases duration of viral shedding
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        | Term 
 | Definition 
 
        | antifungal USE: fingernail and toenail onychomycosis (6 or 12 weeks-daily dose)
 SE: pt monitored for hepatic dysfunction
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        | Term 
 | Definition 
 
        | antifungal USE: common dermatophyte infections-tinea infections of scalp and nonhairy skin, fingernails and toenails-relapse is common
 SE: diarrhea, photosensitivity, headaches
 CI: porphyria, hepatic failure, long-term use requires periodic evaluation of liver, hematopoietic and liver function
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        | Term 
 | Definition 
 
        | antifungal SE: may interfere with ventricular function -> thorough cardiac examination and monitoring
 CI: with midazolam or triazolam b/c prolong the sedative and hypnotic effects; use with HMG-CoA reductase inhibitors increases risk of rhabdomyolysis
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        | Term 
 | Definition 
 
        | antifungal USE: cutaneous infections cause by epidermophyton, microsporium, trichophyton fungi
 TOX: gynecomastia, hepatitis, increased liver function enzymes, long-term use-periodic evaluation
 CI: with midazolam or triazolam b/c prolong the sedative and hypnotic effects; use with HMG-CoA reductase inhibitors increases risk of rhabdomyolysis
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        | Term 
 
        | Bacitracin, Clindamycin, Metronidazole, Mupriocin, Neomycin, Polymixin |  | Definition 
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        | Term 
 | Definition 
 
        | immunomodulator MOA: stimulate IFN-a release from peripheral mononuclear cells and macrophages
 USE: perianal and external genital warts
 -applied topically
 SE: inflammatory rxn at site of application
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        | Term 
 | Definition 
 
        | immunomodulator MOA: block release by mast cells of various inflammatory mediators
 USE: atopic dermatitis
 SE: burning sensation at application site
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        | Term 
 | Definition 
 
        | trichogenic -5-alpha reductase inhibitor
 MOA: blocks conversion of testosterone to dihydrotestosterone
 USE: promotes hair growth, prevents further hair loss
 -treat for at least 3-6 months, continued treatment to sustain benefit
 SE: decrease libido, ejaculation disorder, erectile dysfunction
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        | Term 
 | Definition 
 
        | trichogenic -reverse progressive miniaturization of terminal scalp hairs
 -effect is not permanent and cessation of txt leads to hair loss in 4-6 months
 -percutaneous absorption in normal scalp is minimal, but possible effects on blood pressure (monitor pts with cardiac disease)
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        | Term 
 | Definition 
 
        | antipruitic USE: relief in pruitis associated with atopic dermatitis or lichen simplex chronicus
 MOA: unknown
 SE: drowsiness, anticholinergic effects, allergic dermatitis
 CI: pts with untreated narrow-angle glaucoma or tendency to urinary retention
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        | Term 
 | Definition 
 
        | keratolytic topical-absorbed percutaneously -> excreted in urine
 MOA: solubilize cell surface proteins that keep stratum corneum intact -> desquamation of keratotic debris
 TOX: salicylism, if toxic use hemodialysis
 -children at high risk, careful use in pts with diabetes or peripheral vascular disease
 SE: urticarial, anaphylactic, erythema multiforme rxs in pts allergic to salicylates
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        | Term 
 | Definition 
 
        | anti-inflammatories, anti-pruitic USE: psoriasis, dermatitis, lichen simplex, chronicus
 SE: folliculitis, phototoxicity, allergic contact dermatitis
 -in pts with erythrodermal or generalized pustular psoriasis -> risk of total body exfoliation
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        | Term 
 
        | Betamethasone, Hydrocortisone |  | Definition 
 
        | anti-inflammatories, corticosteroids very responsive: atopic dermatitis, seborrheic dermatitis
 less responsive: psoriasis of palms and soles, vitiligo
 least responsive: intralesional therapy (keloids, cysts)
 -topical prep-variable absorption from healthy skin, increased absorption in damaged skin
 SE: depressed, cigarette-like skin, steroid rosacea
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        | Term 
 | Definition 
 
        | psoriasis treatment MOA: immunosuppressive protein-blocks lymphocyte activation
 USE: moderate-severe chronic plaque psoriasis
 -administered IM
 -not to be used in pts with clinically significant infection or history of cancer
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        | Term 
 | Definition 
 
        | psoriasis treatment MOA: synthetic vit D3 derivative
 USE: plaque-type psoriasis vulgaris of moderate severity
 -improvement noted after 2 weeks of treatment, continued improvement up to 8 weeks
 SE: burning, itching, dryness of treatment area, avoid facial contact, may produce ocular irritation
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        | Term 
 | Definition 
 
        | psoriasis treatment MOA: acetylenic retinoid prodrug hydrolyzed to active form tazarotenic acid -> binds retinoic acid receptors resulting in modified gene expression
 -MOA in psoriasis is unknown
 -teratogenic effects
 -cautin if used in women of childbearing potential
 SE: burning, stinging skin sensation, erythema, localized edema-minimize skin exposure
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        | Term 
 | Definition 
 
        | psoriasis treatment MOA: etretinate metabolite
 -effective orally in psoriasis (esp. pustular form)
 TOX: similar to those seen for isotretinoin-hypervitaminosis, teratogenic
 -not used by pregnant females or those who may become pregnant during treatment or for at least 3 years after treatment is discontinued
 -ETHANOL strictly prohibited during treatment and 2 months after discontinuing therapy
 -3 yr restriction in blood donation
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