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flurandrenolide (Cordran, Cordran SP)

 

Classes: Corticosteroids, Topical

Dosing and uses of Cordran, Cordran SP (flurandrenolide)

 

Adult dosage forms and strengths

lotion

  • 0.05%

cream

  • 0.025%
  • 0.05%

ointment

  • 0.05%

tape

  • 4mcg/cm²

 

Inflammatory/Pruritic Dermatoses

Tape: Apply qDay-q12hr

Cream/Lotion: apply qDay-q6hr (typically q8-12hr)

 

Pediatric dosage forms and strengths

lotion

  • 0.05%

ointment/cream

  • 0.025%
  • 0.05%

tape

  • 4mcg/cm²

 

Inflammatory/Pruritic Dermatoses

Tape: Apply qDay-q12hr

Cream/Lotion: apply qDay-q6hr (typically q8-12hr)

Limit to minimum amount necessary for therapeutic efficacy

 

Cordran, Cordran SP (flurandrenolide) adverse (side) effects

Frequency not defined

Skin atrophy

Striae

Acneform lesions

Eruptions

Miliaria

Burning

Irritation

Secondary infection

Hypertrichosis

Acne

Pigmentation changes

HPA suppression (with higher potency used >2 wk)

 

Postmarketing Reports

Skin: Skin striae, hypersensitivity, skin atrophy, contact dermatitis, skin discoloration

 

Warnings

Contraindications

Lesions exuding serum

Intertriginous areas (tape)

Hypersensitivity

Ophthalmic use

 

Cautions

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

Children may exhibit greater susceptibility to corticosteroid-induced HPA axis suppression and Cushing's syndrome due to larger skin surface area to body weight ratio  

Use med to very high potency for <2 wk to reduce local and systemic side effects

Use low potency for chronic therapy

Kaposi's sarcoma reported with prolonged corticosteroid therapy    

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

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

 

Pregnancy and lactation

Pregnancy category: C

Lactation: Excretion in milk unknown; use with caution

 

Pregnancy categories

A: Generally acceptable. Controlled studies in pregnant women show no evidence of fetal risk.

B: May be acceptable. Either animal studies show no risk but human studies not available or animal studies showed minor risks and human studies done and showed no risk.

C: Use with caution if benefits outweigh risks. Animal studies show risk and human studies not available or neither animal nor human studies done.

D: Use in LIFE-THREATENING emergencies when no safer drug available. Positive evidence of human fetal risk.

X: Do not use in pregnancy. Risks involved outweigh potential benefits. Safer alternatives exist.

NA: Information not available.

 

Pharmacology of Cordran, Cordran SP (flurandrenolide)

Mechanism of action

Corticosteroids decrease inflammation by stabilizing leukocyte lysosomal membranes, preventing release of destructive acid hydrolases from leukocytes; inhibiting macrophage accumulation in inflamed areas; reducing leukocyte adhesion to capillary endothelium; reducing capillary wall permeability and edema formation; decreasing complement components; antagonizing histamine activity and release of kinin from substrates; reducing fibroblast proliferation, collagen deposition, and subsequent scar tissue formation

 

Pharmacokinetics

Absorption: Minimal (~1%); nature of skin at application; occlusion and inflammation may increase absorption

Distribution: Throughout local skin

Metabolism: Liver

Excretion: Urine; feces (small amounts)