2004
DOI: 10.1111/j.1365-2222.2004.02098.x
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Prophylactic management of children at risk for recurrent upper respiratory infections: the Preventia I Study

Abstract: The strong decrease in the rate of infections in the children at risk of recurrent infections, while not being influenced by loratadine treatment, should encourage future reflection in terms of prophylactic management. This study also confirms the long-term safety of loratadine and its metabolites in young children.

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Cited by 35 publications
(25 citation statements)
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“…In the prospective, multicenter, randomized, double-blind, placebo-controlled Preventia I study conducted over 12 months in 412 children who had experienced at least five episodes of upper respiratory tract infections, and no more than two episodes of wheezing during the previous 12 months, aged 12-30 months at enrollment, loratadine 5 mg/day (2.5 mg/day for children aged 24 ≤ months) was found to have a similar safety profile to that of placebo, confirming the long-term safety of loratadine in infants [47]. An intentional ingestion of 300 mg loratadine by a 6 years old child was reported without serious adverse effects showing loratadine to have a wide therapeutic index [48].…”
Section: Loratadinesupporting
confidence: 72%
“…In the prospective, multicenter, randomized, double-blind, placebo-controlled Preventia I study conducted over 12 months in 412 children who had experienced at least five episodes of upper respiratory tract infections, and no more than two episodes of wheezing during the previous 12 months, aged 12-30 months at enrollment, loratadine 5 mg/day (2.5 mg/day for children aged 24 ≤ months) was found to have a similar safety profile to that of placebo, confirming the long-term safety of loratadine in infants [47]. An intentional ingestion of 300 mg loratadine by a 6 years old child was reported without serious adverse effects showing loratadine to have a wide therapeutic index [48].…”
Section: Loratadinesupporting
confidence: 72%
“…Cetirizine, fexofenadine and levocetirizine are not metabolized to any extent. Moreover, while many second-generation H 1 -antihistamines are effective and safe in the treatment of allergic rhinitis in children, only cetirizine, levocetirizine and loratadine have been studied for long-term efficacy and safety in children (2230)(2231)(2232).…”
Section: Treatmentmentioning
confidence: 99%
“…These include randomized, controlled, masked studies of 6 to 12 months' duration with desloratadine, fexofenadine, and levocetirizine in adults, and of 12 to 18 months' duration with cetirizine, levocetirizine, and loratadine in very young children [20,21,46-48]. …”
Section: Adverse Effects Of H1 Antihistaminesmentioning
confidence: 99%
“…The long-term safety profiles of cetirizine, levocetirizine, and loratadine are similar to placebo, as confirmed in randomized, masked, controlled trials in young children aged 12 to 36 months. Studies of all 3 medications involved monitoring of adverse event reports, body mass and height measurements, blood hematology and chemistry tests, and for some of them, electrocardiograms, monitoring of developmental milestones and behavior, and objective tests of intellectual performance [46-48]. …”
Section: Adverse Effects Of H1 Antihistaminesmentioning
confidence: 99%