FDA批准异丙托溴铵与硫酸沙丁胺醇复方药物Combivent Respimat 用于采用常规支气管扩张剂气雾剂仍然发生支气管痉挛以及需要第二种支气管扩张剂的慢性阻塞性肺炎(COPD)患者治疗。
http://www.fda.gov/Drugs/DrugSafety/InformationbyDrugClass/ucm274684.htm
FDA Approves Combivent Respimat (ipratropium bromide and albuterol sulfate) Inhalation SprayWhat action is FDA taking today?
FDA is announcing the approval of Combivent Respimat (ipratropium bromide and albuterol sulfate) Inhalation Spray for “patients with chronic obstructive pulmonary disease (COPD) on a regular aerosol bronchodilator who continue to have evidence of bronchospasm and who require a second bronchodilator.” Combivent Respimat contains two different types of medicines that open airways in the lungs to help patients with COPD breathe better.
What is Combivent Respimat?
Combivent Respimat is a suitable alternative for patients who are currently using Combivent (ipratropium bromide and albuterol sulfate) Inhalation Aerosol. Combivent Inhalation Aerosol is being phased out because it contains chlorofluorocarbons (CFCs). CFCs are chemical compounds that decrease the ozone layer. As a result, Combivent Inhalation Aerosol will not be available after December 31, 2013.
Combivent Respimat does not contain CFCs.
Why are CFC inhalers being phased out?
Inhalers that contain CFCs are being phased out due to an international agreement called the Montreal Protocol on Substances that Deplete the Ozone Layer1. By signing this agreement, the United States promised to make it illegal to make or sell substances that decrease the ozone layer. Most inhalers that contain CFCs have already been phased out as part of this agreement. What impact will this have on patients?
Patients who use Combivent Inhalation Aerosol will have another treatment option and a suitable alternative when Combivent Inhalation Aerosol is no longer available.
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