A client receives a subcutaneous omalizumab injection in the… | MyMerci
Adverse Effects/Contraindications/Interactions PPT
Question

A client receives a subcutaneous omalizumab injection in the clinic for severe allergic asthma. Which post-administration practice most reflects the FDA boxed warning?

Explanation
Correct (2): Omalizumab carries an FDA boxed warning for anaphylaxis — life-threatening, can occur with first or any subsequent dose, sometimes delayed up to 24 hours. Observation in a healthcare setting (2 hours initially, 30 minutes for stable later doses) with anaphylaxis kit ready. Self-injectable epinephrine (Auto-Injector) is provided to patient. (1,3) Unsafe. (4) Pre-medication does not eliminate anaphylaxis risk.

In-depth explanation

Memory Tip Omalizumab (anti-IgE) = "Anti-IgE = Anaphylaxis warning." All biologic asthma agents (omalizumab, mepolizumab, benralizumab, dupilumab) carry hypersensitivity warnings.

Clinical scenario

Scenario 28-year-old female with severe allergic asthma receiving omalizumab 300 mg SC every 4 weeks. Clinic-administered.

Key concepts

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For study reference only. Always follow current clinical guidelines and your institution’s protocols.