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Albuterol Related Decreased appetite

Official Government Database Reports868
Online Conversations4

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: Dizziness, Nausea, Drug ineffective, Insomnia, Mood altered, Decreased appetite

Posted By glorialady11183 in fdb.rxlist.com on August 11, 2010 @ 12:00 am

... so I knew when I was running low, now I can't tell. The American version also has tons of side effects that I never felt with my old inhaler. For the past 2 months I've been dizzy, had nausea, have tr...

Druginformer Identified Side Effects: Pain, Decreased appetite

Posted By KellyM in www.dailystrength.org

I still feel that I can not get enough air for my lungs, and it is sometimes painful for me to breathe. I have trouble eating and I can not stand to exercise anymore.

Druginformer Identified Side Effects: Discomfort, Decreased appetite

Posted By clk6389 in www.dailystrength.org

it works to help him some times. but he needs a neb treatment 4-5 times in an hour when he is sick. he eats less when he has to have it that often.

Druginformer Identified Side Effects: Dizziness, Throat irritation, Headache, Dry mouth, Decreased appetite

Posted By hoozzy in drugs.com on December 26, 2004 @ 12:00 am

You may experience some or all of these side effects: dry mouth, irritated throat,dizziness,headache,lightheadedness,heartbur n,loss of appetite,altered taste sensation,restlessness,anxiety,nervousne...

* 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.