Systematic (IUPAC) name | |
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8-chloro-6,11-dihydro-11-(4-piperdinylidene)- 5H-benzo[5,6]cyclohepta[1,2-b]pyridine | |
Clinical data | |
Trade names | Clarinex |
AHFS/Drugs.com | monograph |
MedlinePlus | a602002 |
Licence data | EMA:Link, US FDA:link |
Pregnancy cat. | B1(AU) C(US) |
Legal status | POM (UK) ℞-only (US) |
Routes | oral |
Pharmacokinetic data | |
Bioavailability | Rapidly absorbed |
Protein binding | 85% |
Metabolism | Liver |
Half-life | 27 hours |
Excretion | 40% as conjugated metabolites into urine Similar amount into the feces |
Identifiers | |
CAS number | 100643-71-8 |
ATC code | R06AX27 |
PubChem | CID 124087 |
DrugBank | APRD00324 |
ChemSpider | 110575 |
UNII | FVF865388R |
KEGG | D03693 |
ChEBI | CHEBI:291342 |
ChEMBL | CHEMBL1172 |
Chemical data | |
Formula | C19H19ClN2 |
Mol. mass | 310.82 |
SMILES | eMolecules & PubChem |
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Desloratadine is a drug used to treat allergies. It is marketed under several trade names such as NeoClarityn, Claramax, Clarinex, Larinex, Aerius, Dazit, Azomyr and Delot. It is an active metabolite of loratadine, which is also on the market.
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Desloratadine is available as tablets (including orally disintegrating and extended release) and as syrup.[1] In Colombia (South America) it is marketed under Dexio from Laboratorios Bussié, as tablets and as syrup to children.
Desloratadine is a tricyclic antihistamine, which has a selective and peripheral H1-antagonist action. It is an antagonist at histamine H1 receptors, and an antagonist at all subtypes of the muscarinic acetylcholine receptor. It has a long-lasting effect and in moderate and low doses, does not cause drowsiness because it does not readily enter the central nervous system.[2]
Most common side-effects are fatigue, dry mouth, headache, and gastrointestinal disturbances.
Desloratadine is the major metabolite of loratadine. There are no head-to-head randomised controlled trials of the two drugs. A survey of patients dissatisfied with loratadine published in August 2003 reported equal or better satisfaction with desloratadine,[3] concluding:
When severity of disease was controlled for in the analysis, a pattern emerged suggesting greater levels of satisfaction amongst loratadine dissatisfied patients who converted to desloratadine. Point estimates suggest a consistent pattern favoring desloratadine patient satisfaction, with statistically significant results reported for sum of adverse effects, nighttime awakening due to symptoms, symptom severity just prior to the next dose, and overall satisfaction (p < 0.05).
A November 2003 article published in the journal American Family Physician about the safety, tolerability, effectiveness, price, and simplicity of desloratadine concluded the following:[4]
Desloratadine is similar in effectiveness to fexofenadine and would be expected to produce results similar to loratadine and other nonsedating antihistamines. There is no clinical advantage to switching a patient from loratadine to desloratadine. However, it may be an option for patients whose medical insurance no longer covers loratadine if the co-pay is less than the cost of the over-the-counter product.
In Canada, desloratadine is available without a prescription, and as a generic. Prices are comparable to those of loratadine.
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