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Chlorhexidine Gluconate Related Adverse Event

Official FDA Reports4
Social Media Events4
Active Ingredients
  • Chlorhexidine Gluconate
Additional Terms for Adverse Event
  • Vision Changes
  • Metallic Taste
  • Nasty Taste In My Mouth
  • Exertional
  • Fluctuation
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  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: Horrendous reaction within an hour that continues into a 3rd day without noticeable relief along with additional symptoms. Severe metallic taste , sloughing of mucous membranes, chapped...


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

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Did the author experience adverse event while taking peridex?

What is this?

Peridex

Side Effects: I experienced a very nasty taste in my mouth for several hours after rinsing with peridex .


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

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Did the author experience adverse event while taking peridex?

What is this?

Peridex

Side Effects: Was told to us this because flossing might dislodge the temporary crown . First time I used it I lost the ability to taste on the tip of my tongue. Same area also became numb. Not goo...


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

View full report on drug related adverse event

Did the author experience adverse event while taking peridex?

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Tell us about your Experience with Chlorhexidine Gluconate Related Adverse Event

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Share Your Experience

Druginformer Identified Side Effects: Adverse event, Discomfort, Dry mouth, Swollen tongue, Chapped lips

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

Side Effects: Horrendous reaction within an hour that continues into a 3rd day without noticeable relief along with additional symptoms. Severe metallic taste, sloughing of mucous membranes, chapped...

Druginformer Identified Side Effects: Adverse event

Posted By Anonymous in askapatient.com on May 3, 2013 @ 12:00 am

Side Effects: I experienced a very nasty taste in my mouth for several hours after rinsing with peridex.

Druginformer Identified Side Effects: Hypoaesthesia, Adverse event

Posted By Anonymous in askapatient.com on August 18, 2008 @ 12:00 am

... Effects: Was told to us this because flossing might dislodge the temporary crown. First time I used it I lost the ability to taste on the tip of my tongue. Same area also became numb. Not good.

Druginformer Identified Side Effects: Adverse event

Posted By Anonymous in askapatient.com on September 16, 2005 @ 12:00 am

Side Effects: when used daily, metallic taste...then down to 2 times a week and no side effects except a little staining at my dental hygiene appointments helped to control progression of p...



* 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.