Fexofenadine Hydrochloride
Renal impairment. Pregnancy, lactation; children <6 yr. Lactation: Excretion in milk unknown; use with caution (AAP states “compatible with nursing”)
Seasonal Allergic rhinitis, Hay fever, Chronic Idiopathic Urticaria, Allergy
Hypersensitivity.
N/A
>10% Vomiting (6-12%) 1-10% Headache (5-10%),Cough (4%),Diarrhea (3-4%),URTI (3%),Back pain (2-3%),Pyrexia (2%),Dysmenorrhea (2%),Dizziness (2%),Stomach discomfort (2%),Pain in extremity (2%),Somnolence (1-3%),Rhinorrhea (1-2%)
Fexofenadine, an active metabolite of terfenadine, is a competitive peripheral histamine H1-receptor antagonist on effector cells in the GI tract, blood vessels and respiratory tract.
Co-admin with ketoconazole or erythromycin may increase plasma levels of fexofenadine. May increase adverse effects of other anticholinergics and CNS depressants. May increase arrhythmogenic effect of antipsychotic agents (phenothiazines); avoid concurrent usage. May reduce the efficacy of betahistine. Pramlintide may increase the anticholinergic effect of fexofenadine. Bioavailability may be increased by verapamil. Efficacy may be reduced by rifampin.
Pregnancy category: C Lactation: Excretion in milk unknown; use with caution (AAP states “compatible with nursing”)
Adults: Seasonal Allergic Rhinitis/Chronic Idiopathic Urticaria 60 mg twice daily or 120 mg once daily or 180 mg once daily with water
Children: Seasonal Allergic Rhinitis <2 years: Use not recommended 2-12 years: 30 mg PO BID or 5 ml twice daily >12 years: 60 mg PO BID OR 180 mg PO qDay ODT 6-12 years: 30 mg PO BID Chronic Idiopathic Urticaria <6 months: Use not recommended 6 months-2 years: 15 mg PO BID or 2.5 ml twice daily 2-12 years: 30 mg PO BID >12 years: 60 mg PO BID OR 180 mg PO qDay ODT 6-12 years: 30 mg PO BID
Renal impairment (CrCl <80 mL/min): 60 mg PO qDay initially
Should be taken on an empty stomach. Take before meals. Take with water. Do not take w/ fruit juice. ODT: Allow to disintegrate on tongue, followed by swallowing with or without water;
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