Telgate 180mg Nic medicine supports the treatment of allergic rhinitis, urticaria (2 blisters x 10 tablets)
Dosage form Film bag tablets
Specifications Box of 2 blisters x 10 tablets
Ingredient Fexofenadin HCl
Ingredient
| Composition information | Content |
| Fexofenadin HCl | 180mg |
Uses
Indications
Telgate 180mg drug indicated symptomatic treatment in seasonal allergic rhinitis in adults and children over 6 years old, malefinity chronic urticaria in adults and children over 12 years old.
Pharmacokological
Fexofenadin is a second -generation antihistamine drug, which has a specific antagonistic and selective effect on peripheral H1 receptors. Fexofenadin is a metabolic substance that is active of terfenadin but no longer toxic to the heart due to not inhibiting potassium channel associated with myocardial cycles.
Fexofenadin has no significant effect on acetylcholin antagonism, dopamine antagonism and has no inhibiting receptor of Alpha 1 or beta - adrenergic. At the treatment dose, the drug does not cause sleep or affects the central nervous system. The drug has a fast and prolonged effect due to the slow -attached drug into the H1 receptor, forming a sustainable complex and separating slowly.
pharmacokinetics
The peak concentration in the blood is achieved after 2 to 3 hours. Fat -rich foods reduce the peak concentration in plasma by about 17% and extend the time to reach the peak concentration of the drug (until about 4 hours). Anti -antihistamine effect lasts more than 12 hours.
The ratio of the plasma protein of the drug is 60 to 70%, mainly with albumin and alpha1-acid glycoprotein. It is unclear whether the drug is through the placenta or excretion in breast milk, but when using terfenadin has detected fexofenadin is the metabolism of terfenadin in breast milk.
Fexofenadin does not go through blood-flabbit barriers. Fexofenadin is very little metabolized (about 5%, mainly in the intestinal mucosa. Only about 0.5 to 1.5% are metabolized in the liver thanks to the cytochrom P450 enzyme system into non -active substances). About 3.5% of fexofenadin dose metabolized through phase II (not related to the cytochrom P450 enzyme system) into methyl ester derivatives. This metabolic substance is only seen in the stool, so there may be the participation of intestinal bacteria in this metabolism.
FEXOFENADIN SELLING Time is about 14.4 hours, longer (31-72%) in people with kidney failure. The drug excreted mainly through the kidneys (approximately 80%) and urine (11-12%) in constant form.
Pharmacokinetics in people with renal failure:
Before taking Telgate 180mg Nic medicine supports the treatment of allergic rhinitis, urticaria (2 blisters x 10 tablets)
How to use
Tablets for oral tablets.
Dosage
Specific dose depends on the condition and level of progression of the disease. For a suitable dose, you need to consult a doctor or medical specialist.
What to do when using overdose?
What to do when forgetting 1 dose? However, if the time to relax with the next dose is too short, skip the dose and continue the calendar of the drug. Do not use double dose to compensate for missed dose.
Side Effects
When using Telgate often has unwanted effects (ADR) such as:
Common
Warnings
Before using the drug you need to read the instructions carefully and refer to the information below.
Contraindicated
Telgate drugs contraindicated in the following cases:
Precautions when using
although Fexofenadin is less likely to cause sleepiness, but still need to be cautious when driving or controlling machinery requires alertness.
Be careful and adjust the appropriate dose when taking drugs for people with impaired renal function because the drug level in plasma increases due to prolonged selling time. Be careful while taking the drug for the elderly (over 65 years old) often has renal physiological impairment.
Safety and effectiveness of drugs in children under 6 months of age has not been identified.
Need to stop Fexofenadin at least 24-48 hours before conducting injection antigen tests.
Use fexofenadin to make psoriasis worse.
Patients with cardiovascular disease, people with prolonged QT.
Drug interaction
erythromycin and ketoconazole increases fexofenadin levels in plasma but does not change the QT.
Fexofenadin concentration may increase due to erythromycin, ketoconazole, verapamil, p-glycoprotein inhibitors.
Unsuitable Fexofenadin with antacids containing aluminum, magnesi because it will reduce fexofenadin absorption.
Fexofenadin may increase alcohol concentration, TKTW sedatives, cholinergic substances.
Fexofenadin may reduce the concentration by acetylcholinininininiserase inhibitors (in TKTW), amphetamine, acid antacids, grapefruit juice, rifampin.
Storage
Leave a cool place, avoid light, temperature below 30⁰C.
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