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Ventolin Related Palpitations

Official Government Database Reports243
Online Conversations4

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: Tremor, Throat irritation, Dizziness, Palpitations, Eczema, Muscular weakness, Rash

Posted By Anonymous in askapatient.com on July 22, 2010 @ 12:00 am

Side Effects: shaking and weakness immediately, especially in arms and legs, slightly elevated heart rate (but my heart rate is usually low so within normal range), lightheadedness. The following da...

Druginformer Identified Side Effects: Palpitations, Drug tolerance increased

Posted By Anonymous in askapatient.com on May 20, 2006 @ 12:00 am

Side Effects: terrible palpitations I've been taking ventolin since I was a kid, but it stopped working for me. I spent a year with terrible asthma attacks before the doctors realized the ...

Druginformer Identified Side Effects: Tremor, Palpitations

Posted By Anonymous in everydayhealth.com on December 21, 2004 @ 12:00 am

... used it. I am now back to using it 3-4 times weekly and now each time I use it, it clears me up almost instantly. I have not had any side effects, except involuntary shaking (hands) and palpitations, ...

Druginformer Identified Side Effects: Palpitations, Skin tightness, Discomfort

Posted By Anonymous in everydayhealth.com on April 19, 2002 @ 12:00 am

effective, but... Relieves tightness effectively, but racing pulse is uncomfortable. Best used only occasionally. If you are using this more than a few times a week you need to up the dose of Steroid...

* 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.