TUDORZA PRESSAIR Reviews (ACLIDINIUM BROMIDE)

Average Rating: 5.0 (1 Ratings)

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 Type: Rx Drug

  

TUDORZA PRESSAIR  (ACLIDINIUM BROMIDE):  Aclidinium is used to control and prevent symptoms (such as wheezing, shortness of breath) caused by ongoing lung disease (chronic obstructive pulmonary disease-COPD which includes bronchitis and emphysema). It works by relaxing the muscles around the airways so that they open up and you can breathe more easily. Aclidinium belongs to a class of drugs known as anticholinergics. Controlling symptoms of breathing problems can decrease time lost from work or school. This medication must be used regularly to be effective. It does not work right away and should not be used to relieve sudden breathing problems. If wheezing or sudden shortness of breath occurs, use your quick-relief inhaler (such as albuterol, also called salbutamol in some countries) as prescribed.   FDA Approval Date: 2012-07-23 (Sources: U.S. Centers for Medicare Services, FDA)

  

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RATING  REASONSIDE EFFECTS FOR TUDORZA PRESSAICOMMENTSSEXAGEDURATION/
DOSAGE		DATE ADDED
 
 5  Asthma Headaches at first but went away as my body adjusted to the medication. Works great!!! M 35 5 months
400 mcg		 2/6/2015
  

TUDORZA PRESSAIR  (ACLIDINIUM BROMIDE):  Aclidinium is used to control and prevent symptoms (such as wheezing, shortness of breath) caused by ongoing lung disease (chronic obstructive pulmonary disease-COPD which includes bronchitis and emphysema). It works by relaxing the muscles around the airways so that they open up and you can breathe more easily. Aclidinium belongs to a class of drugs known as anticholinergics. Controlling symptoms of breathing problems can decrease time lost from work or school. This medication must be used regularly to be effective. It does not work right away and should not be used to relieve sudden breathing problems. If wheezing or sudden shortness of breath occurs, use your quick-relief inhaler (such as albuterol, also called salbutamol in some countries) as prescribed.   FDA Approval Date: 2012-07-23 (Sources: U.S. Centers for Medicare Services, FDA)

     

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