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Albuterol Related Nausea

Official Government Database Reports2,955
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, Somnolence

Posted By Anonymous in fdb.rxlist.com on August 21, 2010 @ 12:00 am

it works ok but not always, and the nausea and dizziness accompanied by fatigue made me stop

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: Nausea, Hypersensitivity

Posted By ResilientWoman in www.dailystrength.org

Prefer to use it in my nebulizer. I have trouble with the propellants in asthma inhalers. Sometimes I'm allergic to them. Sometimes they just make me nauseous. No side effects with nebulizer prepa...

Druginformer Identified Side Effects: Nausea

Posted By Aurora60 in healingwell.com on January 11, 2009 @ 12:00 am

... I only use albuterol if I am having a really bad day. Otherwise I use symbicort as my long term inhaler and I never have any side effects anymore. At first I had a litle nausea but it passed quickl...

* 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.