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(Pediatrics in Review. 2006;27:315-317.)
© 2006 American Academy of Pediatrics
In Brief |
| The first 300 words of the full text of this article appear below. |
Cytochrome P450: New Nomenclature and Clinical Implications. Cupp MJ, Tracy TS. Am Fam Physician. 1998;57 :107 116[Medline]
Drug-Drug Interactions. Reed MD, Blumer JL. In: Haddad LM, Shannon MW, Winchester JF, eds. Clinical Management of Poisoning and Drug Overdose. 3rd ed. Philadelphia, Pa: WB Saunders Company; 1998
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Cytochrome P450 Enzymes: Substrates, Inhibitors, and Inducers. In: Taketomo CK, Hodding JH, Kraus DM. Pediatric Dosage Handbook. 12th ed. Hudson, Ohio: Lexi-Comp; 2005
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A drug interaction occurs when one drug alters the effectiveness or toxicity of another. Clinically significant drug interactions, which pose potential harm to the patient, may result from changes in pharmaceutical, pharmacokinetic, or pharmacodynamic properties. Required in vitro studies conducted by drug manufacturers help predict the potential occurrence of a drug interaction, but they do not confirm the clinical relevance for patients, and they are not sufficiently sensitive to identify all potentially serious interactions, especially in the pediatric population.
Patient factors that increase the risk for drug interactions include being critically ill; receiving polypharmacy; having impaired hepatic or renal function, hypoxemia, or metabolic disturbances; and being elderly. Given the paucity of data on drug interactions in pediatric patients, children also should be considered at special risk. Drug characteristics that contribute to interactions include high potency, wide usage, action on vital organ functions, narrow therapeutic index, saturable hepatic metabolism, and extensive protein binding (>90%).
Drug interactions can be used strategically to benefit patients.
Catherine Tom-Revzon, PharmD
Arnold & Marie Schwartz College of Pharmacy and Health Sciences
Long Island University
Brooklyn, NY
Childrens Hospital at Montefiore
Bronx, NY
Henry M. Adam, MD
Editor, In Brief
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