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Albuterol Related Somnolence

Official Government Database Reports664
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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: Agitation, Sleep disorder, Crying, Mania, Somnolence

Posted By Anonymous in askapatient.com on August 25, 2004 @ 12:00 am

Side Effects: The worst!! I was up ALL NIGHT wired the first night. Finally fell asleep at 6am! Extreme agitation, on edge, tearful. I almost felt manic. Stopped after 24 hours use. Felt like i...

Druginformer Identified Side Effects: Tremor, Somnolence

Posted By Rac87el in www.dailystrength.org

Its my HFA albuterol inhaler its called a rescue inhaler because without it I would quit breathing. It works great, the only side effects is fatigue,and tremors.

Druginformer Identified Side Effects: Somnolence

Posted By abbywondering in www.dailystrength.org

It works, but it makes me drowsy.

Druginformer Identified Side Effects: Somnolence

Posted By helsbells in www.dailystrength.org

since being diagnosed i am on all the right med, they are working but i still have bad days and i feel so tired all the time

Druginformer Identified Side Effects: Somnolence, Psychotic disorder

Posted By Anonymous in ehealthforum.com on September 5, 2008 @ 12:00 am

... can be the result of many conditions (organic and mental) including a side effect from Albuterol. Multivitamin supplements could help you only if the cause of your tiredness was a deficit of 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.