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Generic Name
Fexofenadine hydrochloride
Trade Name
Fenadine
Manufacturer
JPM
Risk Category
C
  • Studies on animals show adverse effect and toxicity on fetus.
  • No adequate and well controlled studies done on pregnant women.
  • Drugs should be given only if the potential benefit outweighs the potential risk to the fetus.
FDA Pregnancy Risk Categories

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Indication
Indication
  • Active metabolite is H1-antihistamine
  • Treatment of symptoms of seasonal allergic rhinitis.
  • Treatment of urticaria.
  • Fetal Risk
    Fetal Risk
  • Not teratogenic but toxic with high doses in animals.
  • Inadequate human studies.
  • Breast Feeding
    Breast Feeding
  • It is not known if Fexofenadine is excreted in human milk.
  • There are no adequate and well-controlled studies in women during lactation.
  • Because many drugs are excreted in human milk, caution should be exercised when Fexofenadine hydrochloride is administered to a nursing woman.
  • Other Trade Names
     
    The information on this Web site is not intended as a substitute for the advice and care of your doctor or other health-care provider. Always consult your doctor if you have any questions about exposures during pregnancy and lactation, and before you take any medications. Please read the Terms and Conditions before using this website.
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