Drug Guide
Alcaftadine
Classification
Therapeutic: Antiallergic (Antihistamine)
Pharmacological: H1 histamine receptor antagonist
FDA Approved Indications
- Allergic conjunctivitis
Mechanism of Action
Alcaftadine is an H1 histamine receptor antagonist that prevents histamine from binding to H1 receptors on conjunctival tissues, thereby reducing allergic response symptoms such as redness, itching, and swelling.
Dosage and Administration
Adult: One drop in the affected eye(s) once daily.
Pediatric: Safety and effectiveness in pediatric patients below 2 years have not been established.
Geriatric: No specific dosage adjustments required, but caution advised due to potential comorbidities.
Renal Impairment: No specific dosage adjustments recommended.
Hepatic Impairment: No specific data; use with caution.
Pharmacokinetics
Absorption: Minimal systemic absorption; primarily local action.
Distribution: Limited data; presumed to be localized in ocular tissues.
Metabolism: Not fully characterized; primarily topical application.
Excretion: Not well defined; systemic levels are low.
Half Life: Approximate ocular tissue half-life not specified; systemic half-life is brief due to minimal absorption.
Contraindications
- Hypersensitivity to alcaftadine or any component of the formulation.
Precautions
- Use with caution in patients with a history of hypersensitivity to other antihistamines.
- Use with caution in patients with active ocular infections; symptom relief may mask underlying conditions.
Adverse Reactions - Common
- Eye discomfort or stinging (Uncommon)
- Unpleasant taste in mouth (Uncommon)
- Other allergic conjunctivitis symptoms like redness or itching (Uncommon)
Adverse Reactions - Serious
- Eye pain, swelling, or vision changes (Rare)
- Hypersensitivity reactions, including rash, swelling, or difficulty breathing (Rare)
Drug-Drug Interactions
- Potential enhanced ocular dryness with other topical ophthalmic agents.
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Monitor for improvement in allergic symptoms and for any adverse reactions.
Diagnoses:
- Risk for infection, manifestation of allergic conjunctivitis
- Risk for injury related to visual disturbances
Implementation: Administer one drop in each affected eye once daily, instruct on proper instillation technique.
Evaluation: Assess symptom relief and monitor for adverse effects.
Patient/Family Teaching
- Instruct patient on proper eye drop administration technique.
- Advise to avoid touching the tip of the dropper to any surface.
- Inform about possible transient visual disturbances or taste disturbances.
- Emphasize adherence to prescribed dosage.
Special Considerations
Black Box Warnings: N/A
Genetic Factors: N/A
Lab Test Interference: None known.
Overdose Management
Signs/Symptoms: Localized irritation, systemic antihistamine effects (rare).
Treatment: Symptomatic treatment; ocular irrigation if necessary.
Storage and Handling
Storage: Store at room temperature, 20°C to 25°C (68°F to 77°F).
Stability: Stable under recommended conditions; discard opened bottles after 4 weeks.