DrugInformer Search

Ventolin Related Pain

Official Government Database Reports516
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 Ventolin

Thank you for sharing your experience with us!

Share Your Experience

Druginformer Identified Side Effects: Tremor, Dizziness, Pain, Cerebrovascular accident, Euphoric mood

Posted By Anonymous in askapatient.com on October 3, 2011 @ 12:00 am

... seemed fine.When mixed with qvar, I almost passed out, lightheaded and immediately my arm hurt and leg all on my left side. I thought I as experiencing a stroke. I was really trembling and didn't know...

Druginformer Identified Side Effects: Chest pain, Pain

Posted By bresky in mdjunction.com on June 12, 2010 @ 12:00 am

I know I sometimes get chest pain as a side effect of the medication mainly because my pulse goes extremely high. I sit at around 150 sometimes when I go in before I even get the nebulizers mainly bec...

Druginformer Identified Side Effects: Pain

Posted By Anonymous in facebook.com on May 14, 2009 @ 12:00 am

... lung function test is accurate. I'm unable to perform exercises longer than 30 seconds before I feel like I need huge gulps of air and my heart beats like a maniac. Oh and also, my legs ache for a few...

* 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.