Lomilan is an antihistamine, anti-allergic.
Pharmacodynamics
Loratadine refers to antihistamine drugs of systemic action, blockers of H1-histamine receptors. It has anti-allergic, antipruritic, antiexudative action. It reduces capillary permeability, prevents the development of tissue edema, relieves spasms of smooth muscles. Antiallergic effect shall develop within 30 minutes after the drug intake, it reaches its maximum effect after 8-12 hours and lasts for 24 hours.
It does not affect CNS and is not addictive.
Pharmacokinetics
Loratadine is quickly and completely absorbed from the gastrointestinal tract. The presence of food slows absorption.Cmax in serum is reached within 1 h after ingestion. Binding to plasma proteins is more than 95%. It is metabolized in the liver with the formation of the active metabolite descarboethoxyloratadine.
It does not penetrate through the BBB. T1/2 is about 8 hours, in the elderly and in chronic alcoholism it increases. It is excreted with the bile and the kidneys.
In chronic renal failure and hemodialysis the pharmacokinetics is almost unchanged.
Indications
Prevention and treatment of the following diseases and conditions:
seasonal and year-round allergic rhinitis;
allergic conjunctivitis;
allergic skin diseases (including chronic idiopathic urticaria);
pseudoallergic reactions;
allergic reactions to insect bites.
Pharmacological effect
Lomilan – antihistamine, antiallergic.
Pharmacodynamics
Loratadine is a systemic antihistamine, a H1-histamine receptor blocker. It has antiallergic, antipruritic, antiexudative effects. Reduces capillary permeability, prevents the development of tissue edema, and relieves spasms of smooth muscles. The antiallergic effect develops 30 minutes after taking the drug, reaches a maximum after 8–12 hours and lasts 24 hours.
It has no effect on the central nervous system and is not addictive.
Pharmacokinetics
Loratadine is quickly and completely absorbed from the gastrointestinal tract. The presence of food slows down absorption. Cmax in serum is achieved within 1 hour after administration. Communication with plasma proteins is more than 95%. Metabolized in the liver to form the active metabolite descarboethoxyloratadine.
Does not penetrate the BBB. T1/2 is about 8 hours, and increases in older people and chronic alcoholism. Excreted with bile and kidneys.
In chronic renal failure and hemodialysis, the pharmacokinetics remain virtually unchanged.
Active ingredient
Loratadine
Composition
Active ingredient:
loratadine 10 mg;
Excipients:
lactose – 71.3 mg;
corn starch – 15 mg;
gelatinized starch – 3 mg;
magnesium stearate – 0.7 mg
Contraindications
Hypersensitivity to any of the components of the tablets or suspension.
lactase deficiency, lactose intolerance, glucose-galactose malabsorption;
pregnancy;
lactation period;
children under 2 years of age (for suspension); 3 years (for tablets).
With caution: liver failure; severe renal failure (Cl creatinine).
Side Effects
From the immune system: very rarely – anaphylactic reactions.
From the nervous system: often – headache, drowsiness, increased nervous excitability, increased fatigue; infrequently – insomnia; very rarely – dizziness.
From the cardiovascular system: very rarely – tachycardia, rapid heartbeat, syncope, arrhythmia.
From the gastrointestinal tract: infrequently – increased appetite; very rarely – nausea, dry mouth, gastritis.
From the liver and biliary tract: very rarely – impaired liver function.
From the skin: very rarely – allergic reactions (rash), alopecia.
Interaction
Concomitant use of microsomal oxidation inducers (phenytoin, ethanol, barbiturates, rifampicin, tricyclic antidepressants) reduces the effectiveness of loratadine.
Possible interaction of the drug with inhibitors of cytochrome isoenzymes, such as CYP3A4 or CYP2D6 (ketoconazole, quinidine, itraconazole, erythromycin, fluoxetine), increases the concentration of the drug Lomilan® in the blood plasma, which can lead to increased side effects of the drug
Overdose
Symptoms: headache, drowsiness, palpitations, which can last for a long time.
Treatment: when taking an excessive amount of Lomilan®, it is recommended to rinse the stomach and prescribe an adsorbent (activated carbon). There is no specific antidote. Lomilan® is not eliminated by hemodialysis.
To date, it is also unknown whether Lomilan® is eliminated by peritoneal dialysis. After emergency treatment, it is necessary to monitor the patient medically.
Storage conditions
In a dry place, protected from light, at a temperature not exceeding 25 °C
Shelf life
4 years
Manufacturer
Lek d.d., Slovenia
Shelf life | 4 years |
---|---|
Conditions of storage | In a dry, light-protected place at a temperature not exceeding 25 °C |
Manufacturer | Lek d.d., Slovenia |
Medication form | pills |
Brand | Lek d.d. |
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