DrugInformer Search

Albuterol Related Arrhythmia

Official Government Database Reports255
Online Conversations4
Share

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: Arrhythmia

Posted By Anonymous in fdb.rxlist.com on January 17, 2008 @ 12:00 am

oth my son and myself use this drug for asthmatic symptoms...it is very effective.Many cpomplain of the jitters and racing heart,did anyone tell you that you should be using a spacer...EVEN FOR ADULT...

Druginformer Identified Side Effects: Feeling jittery, Arrhythmia

Posted By johnse04 in www.dailystrength.org

Jittery, excessive heartbea

Druginformer Identified Side Effects: Arrhythmia

Posted By stampfreak in www.dailystrength.org

This drug conflicts with my heart arrhythmia so I avoid taking it unless I have no other option.

Druginformer Identified Side Effects: Chest pain, Syncope, Hypersensitivity, Memory impairment, Arrhythmia, Confusional state, Migraine, Muscular weakness

Posted By WillowJ in www.dailystrength.org

Very bad racing heart, maybe chest pain (can't remember for sure), very faint and weak, migraine with confusion. Cannot use. List as allergy/intolerance.


* 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.