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Ventolin Related Headache

Official Government Database Reports629
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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, Headache, Dizziness, Asthma, Cough, Drug ineffective

Posted By Anonymous in askapatient.com on January 11, 2015 @ 12:00 am

Side Effects: Tastes like I'm coughing up paint fumes after usage. Headaches, muscle tremors, dizziness. And it DOESN'T work on my asthma much at all. I'm worse the next day after using it.

Druginformer Identified Side Effects: Headache, Dyspepsia

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

Side Effects: It gives you really bad heartburn if you use this daily. Also headaches. It may have some side effects but without it what would you do. I wouldn't be around.

Druginformer Identified Side Effects: Headache, Feeling jittery, Heart rate increased, Insomnia

Posted By Anonymous in everydayhealth.com on July 4, 2005 @ 12:00 am

Ventolin I hate to use it: the rapid heart rate, jitteryness, headache, insomnia, but use it in a severe attack when I need it: about once a year. Will use one puff if possible

Druginformer Identified Side Effects: Headache

Posted By Anonymous in everydayhealth.com on June 25, 2004 @ 12:00 am

... It only decreased attacks by 40 percent, better than without, but if I had better insurance I would not be using it. Also if I have an attack I also get a really bad headache by using it as a rescue...

* 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.