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Proventil Related Headache

Official Government Database Reports249
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: Cardiac flutter, Weight increased, Headache, Loss of consciousness, Sleep disorder, Palpitations, Euphoric mood

Posted By Anonymous in askapatient.com on March 9, 2011 @ 12:00 am

Side Effects: Light Headed, Passing out, Heart Palpitations, Heavy pounding Heart and Head Aches. Severe stress and lack of sleep as a result of not knowing what was wrong with me for several months...

Druginformer Identified Side Effects: Headache, Cough

Posted By Anonymous in askapatient.com on February 14, 2010 @ 12:00 am

Side Effects: really bad headache the day after, coughing this inhaler works better then pro-air, but the headache I get after is completely unacceptable. BRING BACK CFC INHALERS!!

Druginformer Identified Side Effects: Headache, Feeling jittery, Anxiety

Posted By Anonymous in askapatient.com on October 30, 2007 @ 12:00 am

Side Effects: Jitters/anxiety for a few days after initial use; headaches. I've used it on and off for the last 10 years for mild asthmatic attacks and related bronchitis. The side-effects...

Druginformer Identified Side Effects: Headache, Decreased appetite

Posted By Anonymous in askapatient.com on April 24, 2006 @ 12:00 am


* 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.