DrugInformer Search

Ventolin Related Chest pain

Official Government Database Reports435
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: Chest pain, Dizziness, Vomiting, Anxiety, Panic attack

Posted By Anonymous in askapatient.com on December 21, 2012 @ 12:00 am

Side Effects: Horrible ! Dizzy, vomitting, Chest pains, and really bad anxiety and panic attacks.Heart beating really fast.

Druginformer Identified Side Effects: Chest pain

Posted By pljohns in forums.webmd.com on June 27, 2011 @ 12:00 am

... wanted to try me on Dulera and see if I could get off the neb twice a day and the separate inhaled steroid. It worked great, but the side effects about got me. I had TERRIBLE chest pain and major acid...

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...

* 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.