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Frequently bought together
DESLIN 5/MG FC TAB 30/TAB
- Sku : I-021593
Key features
DESLIN 5 mg film-coated tablets contain the active ingredient desloratadine, a second-generation (non-sedating) H1-antihistamine. It selectively antagonizes peripheral histamine H1 receptors to reduce histamine-mediated allergic symptoms such as sneezing, rhinorrhea, pruritus and wheals. DESLIN is indicated for symptomatic relief of seasonal and perennial allergic rhinitis and for chronic idiopathic urticaria. Available over-the-counter in a pack of 30 film-coated tablets.- Brand: DESLIN
- Active Ingredient: DESLORATADINE
- Strength: 5mg
- Dosage Form: Film-coated tablet
- Pack Size: 30 Tablets
- Route: Oral use
- Prescription Status: OTC
- Therapeutic Class: Antiallergic
- Pharmacological Group: Other Antihistamines
- Drug Class: Second-generation (non-sedating) H1-antihistamine; active metabolite of loratadine.
- Manufacturer: AJA PHARMACEUTICAL INDUSTRIES
- Country of Origin: Saudi Arabia
- SFDA Registration No.: 1608222495
- Shelf Life: 36 months
- Storage: store below 30°c
- Symptom Target: Allergy, Runny Nose
- Sedating: No
Frequently bought together
Indications
Approved Uses
Allergic rhinitis (seasonal and perennial) and chronic idiopathic urticaria.
Off-Label Uses
Allergic conjunctivitis; pruritus associated with atopic dermatitis (symptomatic relief).
Dosage & Administration
Dosing by Condition
Allergic rhinitis or chronic idiopathic urticaria: Adults and adolescents ≥12 years: 5 mg orally once daily.
Initial Dose
5 mg once daily.
Maintenance Dose
5 mg once daily.
Maximum Dose
5 mg once daily.
Children's Dosage
Not recommended for children under 12 years with this tablet formulation; pediatric doses specified for oral solution or other forms.
Dose Adjustment Notes
In renal or hepatic impairment, consider a starting regimen of 5 mg every other day (particularly in severe impairment).
How to Take
Swallow the 5 mg film-coated tablet whole with water; may be taken with or without food; take once daily.
Side Effects
Common Side Effects
Headache, pharyngitis, dry mouth, fatigue, somnolence, myalgia, nausea, dizziness, dysmenorrhea.
Side Effect Frequency
Common (≥1% to <10%): fatigue, dry mouth, headache; other reported adverse effects include somnolence and dizziness (frequency varies by source/age group). Rare/very rare: hypersensitivity reactions (including anaphylaxis/angioedema), tachycardia/palpitations, seizures, and hepatitis/elevated liver enzymes.
Safety & Warnings
Contraindications
Hypersensitivity to desloratadine, loratadine, or any excipients/components of the formulation.
Warnings & Precautions
Use with caution in severe renal impairment and severe hepatic impairment; caution in patients with a history of seizures (particularly children); monitor for hypersensitivity reactions.
Age Restriction
This product is a 5 mg film‑coated tablet; use is generally for adults and adolescents ≥12 years (younger children require age‑appropriate formulations such as oral solution).
Driving Warning
May Cause Drowsiness
Drug Interactions
Drug Interactions
Potential increased desloratadine exposure with strong/moderate metabolic inhibitors reported in studies (e.g., ketoconazole, erythromycin, azithromycin, fluoxetine, cimetidine); alcohol/CNS depressants may add to drowsiness in susceptible patients.
Interaction Severity
MODERATE: Strong/moderate CYP/P-gp inhibitors such as ketoconazole, erythromycin, fluoxetine, and cimetidine may increase desloratadine exposure; clinical significance is usually low. MINOR/CAUTION: Alcohol/CNS depressants-possible additive drowsiness in susceptible patients.
Food Interaction
No restriction.
Alcohol Interaction
Avoid
Special Populations
Pregnancy
Consult Doctor
Breastfeeding
Consult Doctor
Children
Not recommended for children under 12 years with this tablet formulation; pediatric doses specified for oral solution or other forms.
Elderly
Standard adult dosing; no specific dose adjustment required, but use with caution if renal function is reduced
Kidney Impairment
Adults with renal impairment: 5 mg every other day.
Liver Impairment
Adults with hepatic impairment: 5 mg every other day.
Storage & Patient Advice
Stopping the Medicine
Safe to stop anytime
Overdose
Symptoms may include somnolence, tachycardia, and headache; manage with standard supportive care and consider measures to reduce absorption if recent ingestion; desloratadine is not removed by hemodialysis; seek medical attention/poison center advice.
Patient Counseling
Take 1 tablet (5 mg) once daily with or without food; may cause drowsiness in some-use caution with driving until you know your response; avoid alcohol if it makes you sleepy; do not exceed the recommended dose; store below 30°C; seek medical advice if pregnant/breastfeeding or if you have significant kidney/liver disease or persistent/worsening symptoms.
Monitoring Requirements
No routine monitoring
Pharmacology
Mechanism of Action
Selective peripheral histamine H1-receptor antagonist that blocks histamine-mediated allergic symptoms (e.g., sneezing, rhinorrhea, pruritus, wheals).
Onset of Action
Within 3 hours.
Duration of Effect
24 hours.
Bioavailability
Desloratadine is well absorbed with measurable plasma levels within ~30 minutes; Tmax occurred at approximately 3 hours post dose; neither food nor grapefruit juice had an effect on the bioavailability.
Metabolism
Hepatic metabolism: desloratadine is metabolized to 3-hydroxydesloratadine (followed by glucuronidation); the specific CYP enzymes responsible are not definitively established, and a subset of patients are poor metabolizers with higher systemic exposure.
Product Information
Available Dosage Forms
Film-coated tablet; oral solution (syrup).
Composition per Dose
Each film-coated tablet: 5 mg desloratadine
Generic Availability
Yes
OTC Alternatives
Loratadine, cetirizine, and fexofenadine (typical adult OTC doses: loratadine 10 mg daily; cetirizine 10 mg daily; fexofenadine 120-180 mg daily depending on indication).
Symptom Target
Allergy, Runny Nose
Sedating
No
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