DrugInformer Search

Proventil Related Anxiety

Official Government Database Reports214
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.

Tell us about your Experience with Proventil

Thank you for sharing your experience with us!

Share Your Experience

Druginformer Identified Side Effects: Feeling jittery, Anxiety, Abasia

Posted By Anonymous in askapatient.com on May 1, 2008 @ 12:00 am

Side Effects: Jitteryness, major anxiety I took this (2 puffs before exercise) about 4 times but couldn't stand the anxiety and jitters. Doc said to try MaxAir.

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: Anxiety, Decreased appetite

Posted By Anonymous in askapatient.com on August 22, 2006 @ 12:00 am

Side Effects: loss of appetite, some anxiety seems to help ease breathing somewhat. Only took one spray each day.

Druginformer Identified Side Effects: Tremor, Anxiety, Insomnia

Posted By Anonymous in askapatient.com on January 27, 2006 @ 12:00 am

Side Effects: sleeplessness and anxiety. Tremors

* 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.