SPIRIVA RESPIMAT Reviews (TIOTROPIUM BROMIDE)

Average Rating: 1.0 (1 Ratings)

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 Type: Rx Drug

  

SPIRIVA RESPIMAT  (TIOTROPIUM BROMIDE):  Tiotropium is used to treat lung diseases such as asthma and COPD (bronchitis, emphysema). It must be used regularly to prevent wheezing and shortness of breath. It works by relaxing the muscles around the airways so that they open up and you can breathe more easily. Tiotropium 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: 2014-09-24 (Sources: U.S. Centers for Medicare Services, FDA)

  

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RATING  REASONSIDE EFFECTS FOR SPIRIVA RESPIMACOMMENTSSEXAGEDURATION/
DOSAGE		DATE ADDED
 
 1  Asthma Chest pain, skin irritation, burning sore throat, insomnia The sore throat occurred the first day as did minor pain in left breast and 'burning' sensation on the skin of my back. F 45 1 weeks
2.5 MG 1X day		 4/17/2016
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SPIRIVA RESPIMAT  (TIOTROPIUM BROMIDE):  Tiotropium is used to treat lung diseases such as asthma and COPD (bronchitis, emphysema). It must be used regularly to prevent wheezing and shortness of breath. It works by relaxing the muscles around the airways so that they open up and you can breathe more easily. Tiotropium 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: 2014-09-24 (Sources: U.S. Centers for Medicare Services, FDA)

     

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