“May all be happy, may all be healed, may all be at peace and may no one ever suffer."
Fexofenadine Hydrochloride is an antihistamine with selective peripheral H1-receptor antagonist activity. It is rapidly absorbed after oral administration and peak plasma concentration is reached in 2-3 hours. It does not appear to cross the blood brain barrier.
Fexofenadine Hydrochloride is indicated for the relief of symptoms associated with seasonal allergic rhinitis in adults and children. It is also indicated for the treatment of uncomplicated skin manifestations of chronic idiopathic urticaria.
Seasonal Allergic Rhinitis-
Adults and children 12 years and older:
Children from 6 to 11 years:
Children from 2 to 11 years
Chronic Idiopathic Urticaria-
Adults and children 12 years and older:
Children from 6 to 11 years:
Children from 6 months to less than 2 years:
Children from 2 to 11 years:
Contraindicated in patients with known hypersensitivity to Fexofenadine Hydrochloride or any of its ingredients.
Common side effects are headache, fatigue, drowsiness, nausea, dry mouth and gastrointestinal disturbances.
Overdose Effects
In case of an overdose, standard measures to remove any unabsorbed drug should be employed. Symptomatic and supportive treatment is recommended. There has been no reported case of an acute overdose of Fexofenadine hydrochloride.
Caution should be exercised in elderly patient and patient with decreased renal function.
Pregnancy & Lactation
US FDA pregnancy category of Fexofenadine Hydrochloride is C. So, Fexofenadine Hydrochloride should be avoided in pregnancy and lactation unless the potential benefits to the other outweigh the possible risks to the fetus.