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5 Cards in this Set

  • Front
  • Back
1. List the four “non-sedating” anti-histamines (minor dry mouth).
• Loratadine (Claritin)
• Fexofenadine (Allegra)
• Cetirizine (Zyrtec)
• Desloratadine (Clarinex)
2. List the two sedating anti-histamines (significant dry mouth).
• Diphenhydramine (Benadryl)
• Chlorpheniramine (Chlor-Trimeton)
3. Describe the differences between the H1 and H2 receptors.
The H1 receptor is associated with hay fever reactions. The H2 receptor is associated with gastric acidity and will be described under drugs which lower gastric acidity.
4. For the prototypical “non-sedating” antihistamine cetirizine (Zyrtec), describe its use, pharmacologic category, mechanism of action and adverse effects having incidence greater than 10%. (From DIHD)
• Use
o perennial and seasonal allergic rhinitis and other allergic symptoms including urticaria; chronic idiopathic urticaria
• Pharmacologic category
o Histamine H1 Antagonist (Second generation)
• Mechanism
o Competes with histamine for H1-receptor sites on effector cells in the gastrointestinal tract, blood vessels, and respiratory tract
• Adverse effects having incidence greater than 10%
o CNS: Headache, somnolence
5. For the prototypical “sedating” antihistamine diphenhydramine (Benadryl), describe its use, pharmacologic category and mechanism of action. (From DIHD)
• Use
o Symptomatic relief of allergic symptoms caused by histamine release including nasal allergies and allergic dermatosis; adjunct to epinephrine in the treatment of anaphylaxis; nighttime sleep aid; prevention or treatment of motion sickness; antitussive; management of Parkinsonian syndrome including drug-induced extrapyramidal symptoms; topically for relief of pain and itching associated with insect bites, minor cuts and burns, or rashes due to poison ivy, poison oak, and poison sumac
• Pharmacologic category
o Histamine H1 Antagonist (First Generation)
• Mechanism of action
o Competes with histamine for H1-receptor sites on effector cells in the gastrointestinal tract, blood vessels, and respiratory tract; anticholinergic and sedative effects are also seen