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Desloratadine

Antihistamine

Antihistamine
CDSCO approved
EXCRETION
not curated
INTERACTIONS
none in our sources
PREGNANCY
Most manufacturers advise avoiding use during pregnancy; however, there is no evidence of teratogenicity.
FDA category + note

Mechanism

Desloratadine is a second-generation H1 antagonist that causes less sedation and psychomotor impairment than older antihistamines because it penetrates the blood brain barrier only to a slight extent. Its effect is confined to the suppression of symptoms attributable to histamine released by antigen-antibody reactions.

Indications

Symptomatic relief of allergic rhinitisSymptomatic relief of urticariaSymptomatic relief of chronic idiopathic urticariaallergic rhinitisconjunctivitishay feverpollinosisurticariadermographismatopic eczemaacute allergic reactions to drugs and foods

Dosing

Adult
5 mg once daily by mouth
Pediatric
Child 1 5 years: 1.25 mg once daily by mouth; Child 6 11 years: 2.5 mg once daily by mouth; Child 12 17 years: 5 mg once daily by mouth
Renal adjustment
In adults and children: Use half normal dose if eGFR 30 50 mL/minute/1.73 m2. Use half normal dose and reduce dose frequency to alternate days if eGFR 10 30 mL/minute/1.73 m2. Avoid if eGFR less than 10 mL/minute/1.73 m2. Use with caution in severe impairment.

Pharmacokinetics

Bioavailability
DL: —
Protein binding
DL: 82–87%
Metabolism
Metabolite of loratadine
Excretion
DL: —

Contraindications

  • Hypersensitivity to loratadine

Side effects

Common
AstheniaDry mouthHeadachenon-interference with psychomotor performance
Serious
  • Akathisia
  • Arrhythmias
  • Diarrhoea
  • Dizziness
  • Drowsiness
  • Gastrointestinal discomfort
  • Hallucination
  • Hepatic disorders
  • Insomnia
  • Myalgia
  • Nausea
  • Palpitations
  • Seizure
  • Vomiting
  • Abnormal behavior
  • Photosensitivity reaction
  • QT interval prolongation

Pregnancy & lactation

Pregnancy

Most manufacturers advise avoiding use during pregnancy; however, there is no evidence of teratogenicity.

Lactation

Most antihistamines are present in breast milk in varying amounts; although not known to be harmful, most manufacturers advise avoiding their use in mothers who are breast-feeding.

Drug interactions

Alcohol
Moderate
Database

Additive CNS depressant effects, potentially leading to increased drowsiness, sedation, impaired psychomotor performance, and reduced alertness.

Advise patients to avoid or limit alcohol consumption while taking desloratadine, especially during activities requiring mental alertness (e.g., driving, operating machinery). While desloratadine is less sedating than older antihistamines, the combination with alcohol can still be problematic.

Cimetidine
Moderate
Database

Increased plasma concentrations of desloratadine and its active metabolite, 3-hydroxydesloratadine, leading to a potential for increased antihistaminic effects.

Monitor for increased antihistaminic effects (e.g., sedation). While desloratadine has a good safety profile, caution is advised. Dose adjustment of desloratadine is generally not required based on current evidence, but individual patient response should be considered.

Clarithromycin
Moderate
Database

Increased plasma concentrations of desloratadine and its active metabolite, 3-hydroxydesloratadine, leading to a potential for increased antihistaminic effects. While desloratadine has a good cardiac safety profile, the combination with other QTc-prolonging drugs should be considered with caution.

Monitor for increased antihistaminic effects (e.g., sedation). While desloratadine has a good safety profile, caution is advised, especially in patients with pre-existing cardiac conditions. Dose adjustment of desloratadine is generally not required based on current evidence, but individual patient response should be considered.

Erythromycin
Moderate
Database

Increased plasma concentrations of desloratadine and its active metabolite, 3-hydroxydesloratadine, leading to a potential for increased antihistaminic effects. While desloratadine has a good cardiac safety profile, the combination with other QTc-prolonging drugs should be considered with caution.

Monitor for increased antihistaminic effects (e.g., sedation). While desloratadine has a good safety profile, caution is advised, especially in patients with pre-existing cardiac conditions. Dose adjustment of desloratadine is generally not required based on current evidence, but individual patient response should be considered.

Source: DDInter

Ketoconazole
Moderate
Database

Increased plasma concentrations of desloratadine and its active metabolite, 3-hydroxydesloratadine, leading to a potential for increased antihistaminic effects and possibly a slight increase in QTc interval, though generally not clinically significant with desloratadine alone.

Monitor for increased antihistaminic effects (e.g., sedation). While desloratadine has a good safety profile, caution is advised, especially in patients with pre-existing cardiac conditions. Dose adjustment of desloratadine is generally not required based on current evidence, but individual patient response should be considered.

Source: DDInter

Ritonavir
Moderate
Database

Significantly increased plasma concentrations of desloratadine and its active metabolite, 3-hydroxydesloratadine, leading to a potential for increased antihistaminic effects and possibly a slight increase in QTc interval, though generally not clinically significant with desloratadine alone.

Monitor closely for increased antihistaminic effects (e.g., sedation). While desloratadine has a good safety profile, the magnitude of interaction with potent inhibitors like ritonavir warrants caution. Consider using an alternative antihistamine or reducing the desloratadine dose if adverse effects occur.

6 additional low-confidence interactions hidden — those rows lack a documented mechanism or management plan in our sources.

Related guidelines

Other Antihistamine drugs

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Sources: KD Tripathi 7e, Goodman & Gilman 14e, Katzung, BNF·Verified: 2026-05-10 · House clinical team