DrugInformer Search

Chlorhexidine Gluconate Related Dyspnoea

Official FDA Reports205
Social Media Events3
Active Ingredients
  • Chlorhexidine Gluconate
Additional Terms for Dyspnoea
  • Shortness Of Breath
  • Difficulty Breathing
  • Trouble Breathing
  • Breathlessness
  • Sob
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 Chlorhexidine Gluconate.


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

Peridex

Side Effects: An hour after second use, my face, tongue, and throat area started to swell. I started to feel that I was starting to have difficulty breathing . I immediately rinsed mouth out and took ...


Source:" PERIDEX: Side effects, ratings, and pa...

View full report on drug related dyspnoea

Did the author experience dyspnoea while taking peridex?

What is this?

Peridex

Side Effects: nausea and shortness of breath ....burping etc....no I didn't swallow the whole shot....spat it out ..but you're not supposed to spit post op dental bone graft...but this was starting 9 ...


Source:" PERIDEX: Side effects, ratings, and pa...

View full report on drug related dyspnoea

Did the author experience dyspnoea while taking peridex?

What is this?

Peridex

Side Effects: Difficulty breathing for an hour or so after each use, terrible taste in my mouth and extremely dry patchy skin. All went away after discontinued use. And some gastro problems were reli...


Source:" PERIDEX: Side effects, ratings, and pa...

View full report on drug related dyspnoea

Did the author experience dyspnoea while taking peridex?

What is this?

Tell us about your Experience with Chlorhexidine Gluconate Related Dyspnoea

Thank you for sharing your experience with us!

Share Your Experience

Druginformer Identified Side Effects: Hypersensitivity, Dyspnoea, Swelling

Posted By Anonymous in askapatient.com on June 6, 2015 @ 12:00 am

... believe it was related to the rinse. I know it was as it was the only new thing after the dental surgery 2 days ago. The ER staff immediately noticed the allergic reaction and provided necessary care....

Druginformer Identified Side Effects: Eructation, Nausea, Bone graft, Dyspnoea

Posted By Anonymous in askapatient.com on May 2, 2011 @ 12:00 am

Side Effects: nausea and shortness of breath....burping etc....no I didn't swallow the whole shot....spat it out ..but you're not supposed to spit post op dental bone graft...but this was starting 9 ...

Druginformer Identified Side Effects: Flatulence, Dry skin, Dyspnoea, Product taste abnormal

Posted By Anonymous in askapatient.com on December 16, 2009 @ 12:00 am

... Difficulty breathing for an hour or so after each use, terrible taste in my mouth and extremely dry patchy skin. All went away after discontinued use. And some gastro problems were relieved when I qu...



* 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.