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Albuterol Related Irritability

Official Government Database Reports264
Online Conversations5

Extracted from FDA Adverse Event Reports for all drugs with the same active ingredients. To view the active ingredient report, please click here.

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Druginformer Identified Side Effects: Tremor, Feeling jittery, Irritability

Posted By Anonymous in askapatient.com on October 25, 2011 @ 12:00 am

Side Effects: Extreme jittery-ness, shaking, irritability Despite the side effects, I am pro-albuterol. It has saved my life on numerous occasions. I take both the inhaler and the nebulize...

Druginformer Identified Side Effects: Irritability

Posted By Jasonp1978 in www.dailystrength.org

Have used this almost all my life and I'm irritated to hear the generic version will no longer be available.

Druginformer Identified Side Effects: Irritability

Posted By PEENUT22 in www.dailystrength.org


Druginformer Identified Side Effects: Irritability

Posted By sea2006 in forums.webmd.com on January 28, 2009 @ 12:00 am

... which also is what is occuring during an asthma attack in people who *do* have asthma. Side effects will likely be minimal and short-lived (hyperactivity, irritability, etc.) I wouldn't worry about...

Druginformer Identified Side Effects: Diabetes, Acne, Insomnia, Irritability, Menstruation irregular

Posted By orbust in drugs.com on February 29, 2008 @ 12:00 am

... of time can have adverse health affects. Adverse effects of prolonged use of oral steroids such as Albuterol include cataracts, glaucoma, osteoporosis, diabetes, fluid retention, susceptibility to in...

* Warning: The facts and figures contained in these reports are accurate to the best of our capability; however, our metrics are only meant to augment your medical knowledge, and should never be used as the sole basis for selecting a new medication. As with any medical decision, be sure to work with your doctor to ensure the best choices are made for your condition.

* About FAERS: The FDA Adverse Event Reporting System (FAERS) is used by FDA for activities such as looking for new safety concerns that might be related to a marketed product, evaluating a manufacturer's compliance to reporting regulations and responding to outside requests for information. Reporting of adverse events is a voluntary process, and not every report is sent to FDA and entered into FAERS. The FAERS database may contain duplicate reports, the report quality is variable, and many factors may influence reporting (e.g., media attention, length of time a drug is marketed, market share). For these reasons, FAERS case reports cannot be used to calculate incidence or estimates of risk for a particular product or compare risks between products.