DrugInformer Search

Albuterol Related Tachycardia

Official FDA Reports943
Social Media Events5
Active Ingredients
  • Albuterol
Additional Terms for Tachycardia
  • Heart Is Racing Like Crazy
  • Faster Beat
  • Hearth Starts Racing
  • Heart Would Beat Faster Than Usual
  • Heart Beats Faster
Show more

  This report is for all products sharing this active ingredient. For more details, please use our Workbench for research on individual brands like Albuterol.


Explanation

The quarterly trend chart illustrates changing levels of adverse events over time. Results from both the FDA Adverse Event Database (AERS) and adverse events extracted from social media by Druginformer are plotted side-by-side for easy comparison.


List of Possible Side Effects Reported

Report Date Dosage Indication Outcome Country Gender Age Weight (lbs)

* DrugInformer calculates alarm using a proprietary algorithm. Alarm should not be taken as an ofiicial signal from the FDA or other regulatory entity.


Social Media Comments From Around the Web

The following are comments from users that experienced side effects while taking Milnacipran Hydrochloride

Albuterol

severe tachycardia and chest pain often results


Source:" Albuterol

View full report on drug related tachycardia

Did the author experience tachycardia while taking albuterol?

What is this?

Albuterol

major tachycardia


Source:" Albuterol

View full report on drug related tachycardia

Did the author experience tachycardia while taking albuterol?

What is this?

Albuterol

... pocket mistometer and a nebulizer. When I get bad, the only thing that helps is a Prednisone taper. Sometimes taking too much causes headaches and my hearth starts racing

I've tried every ...


Source:" PROVENTIL: Side effects, ratings, and ...

View full report on drug related tachycardia

Did the author experience tachycardia while taking albuterol?

What is this?

Tell us about your Experience with Albuterol Related Tachycardia

Thank you for sharing your experience with us!

Share Your Experience

Druginformer Identified Side Effects: Headache, Tachycardia

Posted By Anonymous in askapatient.com on March 11, 2009 @ 12:00 am

... for all of my 61 years. I use both a pocket mistometer and a nebulizer. When I get bad, the only thing that helps is a Prednisone taper. Sometimes taking too much causes headaches and my hearth sta...

Druginformer Identified Side Effects: Chest discomfort, Tremor, Chest pain, Dizziness, Cardiovascular disorder, Tachycardia, Palpitations, Arrhythmia

Posted By Anonymous in everydayhealth.com on March 31, 2004 @ 12:00 am

... has ended me up in the ER on several occasions over the past few years when my heart was beating greater than 170 bpm and I was having chest pain/dizziness accompanying chest pressure. Plus, I don't k...

Druginformer Identified Side Effects: Chest pain, Tachycardia

Posted By Lynzzie in www.dailystrength.org

severe tachycardia and chest pain often results

Druginformer Identified Side Effects: Tachycardia

Posted By nikitaselias in www.dailystrength.org

major tachycardia

Druginformer Identified Side Effects: Tachycardia, Reversible airways obstruction

Posted By els in healingwell.com on January 20, 2007 @ 12:00 am

... emphysema and reversible airway obstruction. It does induce cardiac stimulation with usage. There for adverse effects with use can be palpitation, tachycardia, hypertension, angina, hypotension, and...



* 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.