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PROAIR® DIGIHALER®
(albuterol sulfate) Inhalation Powder is a prescription medicine used in people 4 years of age and older to:
Do not use PROAIR DIGIHALER if you are allergic to albuterol sulfate, lactose, milk proteins, or any of the ingredients in PROAIR DIGIHALER. Ask your healthcare provider if you have any questions or are not sure
Before using PROAIR DIGIHALER, tell your healthcare provider about all of your medical conditions, including if you:
Tell your healthcare provider about all the medicines you take, especially:
Do not increase your dose or take extra doses of PROAIR DIGIHALER without first talking to your healthcare provider
Get medical help right away if PROAIR DIGIHALER no longer helps your symptoms, your symptoms get worse or you need to use your inhaler more often
While you are using PROAIR DIGIHALER, do not use other inhaled rescue medicines and asthma medicines unless your healthcare provider tells you to do so
PROAIR DIGIHALER may cause serious side effects, including:
The most common side effects of PROAIR DIGIHALER include:
These are not all of the possible side effects of PROAIR DIGIHALER. For more information, ask your healthcare provider or pharmacist
You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch, or call 1-800-FDA-1088
Please see full Prescribing Information for PROAIR DIGIHALER.
AIRDUO DIGIHALER and ARMONAIR DIGIHALER each contain a built-in electronic module that records and stores information about inhaler events. AIRDUO DIGIHALER and ARMONAIR DIGIHALER may be used with, and transmit information to, a mobile App. AIRDUO DIGIHALER and ARMONAIR DIGIHALER do not need to be connected to the app in order for you to take your medicine.
Please see full Prescribing Information for AIRDUO DIGIHALER and ARMONAIR DIGIHALER.
Devices comply with part 15 of the FCC Rules. Operation is subject to the following two conditions: (1) This device may not cause harmful interference, and (2) this device must accept any interference received, including interference that may cause undesired operation. Changes or modifications not expressly approved by Teva could void the user’s authority to operate the equipment.
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