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LORADAY SYRUP
- Sku : I-003653
Key features
LORADAY Syrup is a syrup formulation containing loratadine 1 mg/mL as the active ingredient. It acts as a selective peripheral histamine H1-receptor antagonist (often described as an inverse agonist), reducing histamine-mediated allergic symptoms with minimal central nervous system penetration at usual doses. It is indicated for the symptomatic treatment of seasonal and perennial allergic rhinitis and chronic idiopathic urticaria. Available OTC in a 100 mL syrup.- Brand: LORADAY
- Active Ingredient: LORATADINE 1mg/ml
- Strength: 1mg/ml
- Dosage Form: Syrup
- Pack Size: 100 ml
- Route: Oral use
- Prescription Status: OTC
- Therapeutic Class: Antiallergic
- Pharmacological Group: Other Antihistamines
- Drug Class: Second-generation (peripherally selective) H1-antihistamine with low sedating potential.
- Manufacturer: KUWAIT SAUDI PHARMACEUTICAL INDUSTRIES
- Country of Origin: Kuwait
- SFDA Registration No.: 0801256555
- Shelf Life: 36 months
- Storage: store below 25°c
- Symptom Target: Allergy, Runny Nose
- Sedating: No
Frequently bought together
Indications
Approved Uses
Symptomatic treatment of allergic rhinitis (seasonal/perennial) and chronic idiopathic urticaria.
Dosage & Administration
Dosing by Condition
Allergic rhinitis or urticaria: Adults and children ≥12 years: 10 mg once daily (10 mL of 1 mg/mL syrup). Children 2-11 years: if >30 kg, 10 mg once daily (10 mL); if ≤30 kg, 5 mg once daily (5 mL).
Initial Dose
10mg once daily for adults and children 6 years and older.
Maintenance Dose
10mg once daily for adults and children 6 years and older; 5mg once daily for children 2-5 years.
Maximum Dose
10mg per day for adults and children 6 years and older; 5mg per day for children 2-5 years.
Children's Dosage
Children 2-5 years: 5mg (5ml) once daily. Children 6 years and older: 10mg (10ml) once daily. Not recommended under 2 years. Weight-based dosing (>30kg vs ≤30kg) is not specified in authoritative sources reviewed.
Dose Adjustment Notes
In severe hepatic impairment or severe renal impairment (e.g., CrCl/GFR <30 mL/min), use a lower initial dose or extend the dosing interval (commonly 10 mg every other day in adults).
How to Take
Shake well before use; measure the dose with an oral syringe/medicine spoon; may be taken with or without food; administer once daily as directed.
Side Effects
Common Side Effects
Headache, fatigue, dry mouth; somnolence/drowsiness can occur but is generally uncommon at recommended doses.
Safety & Warnings
Contraindications
Hypersensitivity to loratadine or any excipients
Age Restriction
Not recommended for children under 2 years of age.
Drug Interactions
Drug Interactions
CYP3A4/CYP2D6 inhibitors (e.g., ketoconazole, erythromycin, cimetidine) can increase loratadine/desloratadine exposure; clinically significant effects are uncommon at recommended doses.
Food Interaction
No restriction.
Special Populations
Children
Children 2-5 years: 5mg (5ml) once daily. Children 6 years and older: 10mg (10ml) once daily. Not recommended under 2 years. Weight-based dosing (>30kg vs ≤30kg) is not specified in authoritative sources reviewed.
Kidney Impairment
Severe renal impairment (GFR/CrCl <30 mL/min): adults and children ≥6 years or >30 kg: 10 mg every other day; children 2-5 years: 5 mg every other day.
Storage & Patient Advice
Missed Dose
Take the missed dose when remembered; if it is close to the next dose, skip the missed dose and resume the regular schedule; do not double doses.
Patient Counseling
Shake well and measure doses accurately; take once daily and do not exceed the recommended dose; may be taken with or without food; drowsiness is uncommon but if it occurs avoid driving/alcohol; seek medical advice if symptoms persist/worsen; store below 25°C and keep out of reach of children.
Monitoring Requirements
Patients require monitoring for symptomatic relief, sedation, and potential anticholinergic effects. Renal and hepatic function should be closely monitored in patients with kidney or liver impairment. Cardiac function should be observed in individuals with history of cardiac arrhythmias.
Pharmacology
Mechanism of Action
Selective peripheral histamine H1-receptor antagonist (often described as an inverse agonist) that reduces histamine-mediated allergic symptoms with minimal CNS penetration at usual doses.
Onset of Action
1-3 hours.
Duration of Effect
Approximately 24 hours (supports once-daily dosing).
Half-Life
Loratadine: ~8-12 hours; active metabolite (desloratadine/descarboethoxyloratadine): ~17-24 hours (often cited around ~27 hours in some references).
Bioavailability
Oral bioavailability is not ~100%; loratadine undergoes significant first-pass metabolism and has incomplete systemic availability (commonly cited as ~40% or described as variable).
Excretion
Approximately 40% in urine and ~42% in feces, primarily as metabolites (over ~10 days).
Protein Binding
97-99%.
Product Information
Available Dosage Forms
For this product (LORADAY): Syrup (oral).
Composition per Dose
Each 5ml: Loratadine 5mg (1mg/ml)
Generic Availability
Yes
OTC Alternatives
Other OTC second-generation antihistamines: cetirizine, levocetirizine, fexofenadine; (first-generation option: chlorpheniramine, more sedating).
Symptom Target
Allergy, Runny Nose
Sedating
No
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