Name some nonimmunologic drug reactions. - Nonimmunologic activation of effector pathways, such as direct release of histamine from mast cells and basophils by aspirin, nonsteroidal antiinflammatory drugs (NSAIDs), opiates, polymyxin B, d-tubocurarine, and radiocontrast media
- Overdosage
- Cumulative toxicity, such as the accumulation of drugs or metabolites in the skin (e.g., argyria with the use of silver nitrate spray)
- Normal pharmacologic effects of the drug that are not the primary therapeutic objective (e.g., alopecia following chemotherapy)
- Drug interactions (e.g., administration of ketoconazole may lead to higher levels of cyclosporine and increased toxicity)
- Metabolic changes, such as warfarin producing a hypercoagulable state that results in warfarin necrosis
- Exacerbation of preexisting dermatologic diseases (e.g., lithium can exacerbate acne, psoriasis, and subcorneal pustular dermatosis)
- Ecologic changes, such as antibiotics that reduce the bacteriologic flora, predisposing the patient to candidal infections
- Inherited enzyme or protein deficiencies (e.g., the phenytoin hypersensitivity syndrome occurs in patients deficient in epoxide hydrolase, an enzyme required for metabolism of a toxic epoxide derived from phenytoin)
- Jarisch-Herxheimer phenomenon secondary to bacterial endotoxins and microbial antigens that are liberated from antimicrobial treatment (e.g., a patient with syphilis develops fever, tender lymphadenopathy, arthralgias, and urticaria while being treated with penicillin)
Stern RS, Wintroub BU: Cutaneous reactions to drugs. In Freedberg IM, Eisen AZ, Wolff K, editors: Fitzpatrick’s dermatology in general medicine, ed 5, New York, 1999, McGraw-Hill, pp 1633–1642. |