Mechanism of Action- stimulate beta2-adrenergic receptors, increasing the production of cyclic 3′5′ adenosine monophosphate (cAMP). -Increased cAMP relaxes airway smooth muscle and increases bronchial ciliary activity. Dosage and Time Frame for Response (Short Acting)-have a quick onset (peak effect 10 minutes) and a short duration of action (3–4 hours). -half-life can range from 2.7 hours to 6 hours. -SABAs are indicated for the relief of acute respiratory symptoms in asthma and COPD. Dosage and Time Frame for Response (Long Acting)- include formoterol, salmeterol, and vilanterol. - half-life can range from 5.5 hours to 11 hours. -Formoterol has an onset of action of 3 minutes and a 12-hour duration of action. -Salmeterol has an onset of action of about 2 hours and a 12-hour duration of action. -Vilanterol has an onset of action of about 15 minutes and a 24-hour duration of action. -LABAs are indicated for chronic maintenance therapy in COPD but only with an ICS for asthma. Oral and Paternal Forms-are available but have limited clinical use due to the quick onset of action, ease of administration, beta2-adrenergic specificity, and minimal systemic exposure with the inhaled route of administration. |
Contraindications-contraindicated in persons with a history of hypersensitivity to beta-adrenergic agonists or any component of the formulation. -should be used with caution in patients with known cardiovascular disease, diabetes mellitus, glaucoma, hyperthyroidism, or seizure disorders. Adverse Events (SABA)- Serious events: paradoxical bronchospasm, anaphylaxis, hypersensitivity reaction, angioedema, hypertension, hypotension, angina, cardiac arrest, arrhythmia, hypokalemia, and hyperglycemia. -Common adverse events: throat irritation, upper respiratory infection symptoms, cough, bad taste, tremor, dizziness, nervousness, nausea/vomiting, headache, palpitations, tachycardia, chest pain, pain, and hyperlactatemia. Adverse Events (LABA)-Serious events: paradoxical bronchospasm, asthma exacerbation, asthma-related death, laryngospasm, hypersensitivity reaction, anaphylaxis, hypertension, hypotension, angina, cardiac arrest, arrhythmia, hypokalemia, and hyperglycemia. -Common adverse events: headache, throat irritation, nasal congestion, rhinitis, tracheitis/bronchitis, pharyngitis, urticaria, rash, palpitations, tachycardia, tremor, and nervousness. |
Interactions- sympathomimetic drugs (e.g., catecholamines, catecholamine analogs, amphetamines) increase the risk for beta2-adrenergic agonist adverse effects and toxicities. -Nonselective and higher doses of beta1-selective adrenergic blocking drugs diminish the bronchodilator effects of the beta2-adrenergic agonists. -Concurrent administration of beta-adrenergic agonists and monoamine oxidase inhibitors (MAOIs) or tricyclic antidepressants (TCAs) increases blood pressure and the risk of stroke. Interactions Continued-MAOIs and TCAs must be discontinued at least 14 days prior to initiating. -Thiazide (e.g., hydrochlorothiazide) and loop diuretics (e.g., furosemide) enhance the hypokalemic effects. -The oxazolidinones (e.g., linezolid, tedizolid) enhance the hypertensive effects. -Atomoxetine, a selective norepinephrine reuptake inhibitor indicated for the management of attention-deficit hyperactivity disorder, may increase the tachycardic effects. |
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Beta2 Adrenergic Agonists Cheat Sheet (DRAFT) by eem57
Explanation of Beta2 Adrenergic Agonists
This is a draft cheat sheet. It is a work in progress and is not finished yet.