Indications
Seasonal allergic rhinitis, chronic idiopathic urticaria.
$33.00
Active ingredient: | |
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Dosage form: | |
Indications for use: |
Seasonal allergic rhinitis, chronic idiopathic urticaria.
With caution: Chronic renal failure. (The recommended daily dose in such patients is 60 mg once).
1 coated tablet contains:
active substance:
fexofenadine 180 mg;
excipients:
microcrystalline cellulose,
starch,
lactose,
croscarmellose sodium (primellose),
povidone,
colloidal silicon dioxide,
magnesium stearate,
purified water.
shell:
hydroxypropylmethylcellulose (hypromellose), propylene glycol, purified talc, titanium dioxide, isopropyl alcohol, methylene chloride, dye rolled yellow varnish (for 180 mg tablets).
1 coated tablet contains:
Active ingredient:
fexofenadine 180 mg;
excipients:
microcrystalline cellulose,
starch,
lactose,
croscarmellose sodium (primellose),
povidone,
colloidal silicon dioxide,
magnesium stearate,
purified water.
shell:
hydroxypropylmethylcellulose (hypromellose), propylene glycol, purified talc, titanium dioxide, isopropyl alcohol, methylene chloride, dye rolled yellow varnish (for tablets 180 mg).
Fexofast has an antihistamine, anti-allergic effect. Fexofenadine hydrochloride is a non-sedative H1 – histamine receptor blocker and is a pharmacologically active metabolite of terfenadine.
The antihistamine effect manifests itself 1 hour after ingestion, reaches a maximum in 6 hours and lasts for 24 hours. With repeated use, there was no development of tolerance.
It does not have a choline-and adrenolytic, sedative effect. It does not cause changes in the function of calcium and potassium channels, the QT interval in therapeutic doses.
Pharmacokinetics
After oral use, it is rapidly absorbed from the gastrointestinal tract, the time after reaching the maximum concentration (TCmax) is 1-3 hours.
The average maximum concentration (cmax) after taking 180 mg is approximately 494 ng / ml, after taking 120 mg-427 ng/ml. Plasma protein binding is 60-70% (mainly with albumin and alpha-1-glycoprotein).
It does not cross the blood-brain barrier. The half-life (T 1/2) after repeated use is 14.4 hours.
In patients with moderate (creatinine clearance 41-80 ml/min) and severe (11-40 ml/min) renal insufficiency, T 1/2 increases by 59 and 72%, respectively; in patients on hemodialysis, T 1/2 increases by 31%.
It undergoes partial extrahepatic metabolism (5% of the dose). It is mainly excreted (80%) with bile,11% – unchanged by the kidneys.
Seasonal allergic rhinitis, chronic idiopathic urticaria.
With caution: Chronic renal failure. (The recommended daily dose in such patients is 60 mg once).
Rare (less than 1 case per 1000 appointments):
In some cases:
When combined with erythromycin or ketoconazole, the concentration of fexofenadine in plasma increases 2-3 times.
Taking aluminum-or magnesium-containing antacids 15 minutes before taking fexofenadine leads to a decrease in the bioavailability of the latter (the time interval between taking them should be at least 2 hours).
It does not interact with omeprazole, with drugs that are metabolized in the liver.
Fexofast is taken orally. Adults and children over 12 years of age with chronic idiopathic urticaria-180 mg 1 time a day.
Symptoms: dizziness, drowsiness, and dry mouth.
In case of overdose, it is recommended to carry out standard measures to remove the unabsorbed drug from the gastrointestinal tract.
Symptomatic and supportive care is recommended.
Hemodialysis is ineffective.
When taking the drug Fexofast, it is possible to perform work that requires high concentration of attention and speed of psychomotor reactions (with the exception of people who have a non-standard reaction to medications).
Thus, before starting to perform these tasks (driving vehicles, controlling mechanisms), it is necessary to first check the individual reaction to the drug.
Film-coated tablets
Store in a dry place, protected from light, at temperatures below 25 °C
3 years
Fexofenadine
Tablets
For adults, Children over 12 years of age
Allergy, Hives
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