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Antihistamines & Antiallergics

Fexostad 60

 

Pack size:

Box of 1 blister x 10 film-coated tablets.

 

Composition:

Each film-coated tablet contains fexofenadine hydrochloride 60 mg.

 

Shelf-life:

36 months from the date of manufacturing.

Store in a well-closed container, in a dry place. Do not store above 30oC.

 

  • Indications and Dosage & Administration
  • Contraindications
  • Adverse reactions
  • Precautions

  • Relief of symptoms associated with seasonal allergic rhinitis in adults and children 6 years of age and older. Symptoms treated effectively were sneezing, rhinorrhea, itchy nose/ palate/ throat, itchy/ watery/ red eyes.
    Adults and children 12 years and older:
    60 mg twice daily, or 180 mg once daily. A dose of 60 mg once daily is recommended as the starting dose in patients with decreased renal function.
    Children 6 to 11 years:
    30 mg twice daily. A dose of 30 mg once daily is recommended as the starting dose in pediatric patients with decreased renal function.
  • Treatment of uncomplicated skin manifestations of chronic idiopathic urticaria in adults and children 6 years of age and older. It significantly reduces pruritus and the number of wheals.
    Adults and children 12 years and older:
    60 mg twice daily. A dose of 60 mg once daily is recommended as the starting dose in patients with decreased renal function.
    Children 6 to 11 years:
    30 mg twice daily. A dose of 30 mg once daily is recommended as the starting dose in pediatric patients with decreased renal function.
     
  • For oral administration.
     

Or as advised by physicians.

 

  • Patients with known hypersensitivity to fexofenadine or to any ingredient of the drug.

     

  • The frequency and magnitude of laboratory abnormalities were similar in fexofenadine hydrochloride and placebo treated patients.
  • In rare cases, hypersensitivity reactions include urticaria, pruritus and systemic anaphylaxis have been reported.

     

  • Although clinical experience generally has not revealed differences in responses between geriatric and younger patients to the drug, it should be considered that fexofenadine is substantially excreted by the kidneys and the risk of severe adverse reactions to the drug may be increased in patients with impaired renal function. Because geriatric patients may have decreased renal function, monitoring renal function may be useful and dosage should be selected with caution in these patients.
  • Safety and efficacy of fexofenadine hydrochloride have not been established in children younger than 6 years of age.
  • Pregnancy: There are no adequate and controlled studies to date using fexofenadine in pregnant women, and fexofenadine hydrochloride should be used during pregnancy only when the potential benefits justify the possible risks to the fetus.
  • Lactation: Since there are no adequate and controlled studies to date on the use of fexofenadine during lactation in humans and because many drugs are excreted in human milk, fexofenadine should be used with caution in nursing women, and a decision should be made whether to discontinue nursing or the drug.
  • Effects on ability to drive and use machines: On the basis of the pharmacodynamic profile and reported adverse events it is unlikely that fexofenadine hydrochloride will produce an effect on the ability to drive or use machines. In objective tests, fexofenadine has been shown to have no significant effects on central nervous system function. This means that patients may drive or perform tasks that require concentration. However, in order to identify sensitive people who have an unusual reaction to drugs, it is advisable to check the individual response before driving or performing complicated tasks.

     

Contact us

FACTORY 1: K63/1 Nguyen Thi Soc St., Xuan Thoi Dong, Hoc Mon, HCMC
Tel: +84 28 3718 2141 - Fax: +84 28 3718 2140

FACTORY 2: 40 Tu Do Avenue, VietNam-Singapore Industrial Park, Binh Duong
Tel: +84 274 376 7470 - Fax: +84 274 376 7469
Email : stada@stada.com.vn
Website: www.stada.com.vn



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