DrugInformer Search

Albuterol Related Weight increased

Official Government Database Reports854
Online Conversations3

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

Tell us about your Experience with Albuterol

Thank you for sharing your experience with us!

Share Your Experience

Druginformer Identified Side Effects: Back pain, Pain, Anxiety, Insomnia, Muscle spasms, Weight increased

Posted By Anonymous in drugs.com on November 2, 2013 @ 12:00 am

My doctor put me on a dosage of 2 puffs every 4 hours as needed but when I used this amount I developed almost continuous anxiety attacks, insomnia, back and arm pain, wheezing, muscle spasm and jerki...

Druginformer Identified Side Effects: Cardiac flutter, Weight increased

Posted By rua in www.dailystrength.org

It works but tends to make my heart race and pound a bi

Druginformer Identified Side Effects: Weight increased, Cushingoid

Posted By converse4 in healingwell.com on April 21, 2011 @ 12:00 am

about a month ago I was hospitalized for the first time ever and was on constant albuterol for two days and was taking massive amounts of Prednisone. I was in the ICU and at the hospital for 8 days a...

* 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.