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Chlorhexidine Gluconate Related Hypersensitivity

Official FDA Reports22
Social Media Events3
Active Ingredients
  • Chlorhexidine Gluconate
Additional Terms for Hypersensitivity
  • Allergic
  • Alleregic Reaction
  • Sensitive Finger Tips
  • Sensitivity To Many Things
  • Allergies Worsened
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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

... 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....


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

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Did the author experience hypersensitivity while taking peridex?

What is this?

Peridex

... two uses; this was similar to the 'pins & needles' sensation of a limb that falls asleep. This alarmed me and caused me to call my dentist, who told me that I am likely hypersensitive to the active in...


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

View full report on drug related hypersensitivity

Did the author experience hypersensitivity while taking peridex?

What is this?

Chlorhexidine Gluconate

Chlorhexidine Gluconate under the brand name Chloraprep was used on my skin prior to a surgical procedure to prevent infection. I've had a severe allergic reaction to it, with hives, rash, itching, re...


Source:" chlorhexidine gluconate MM : User Rati...

View full report on drug related hypersensitivity

Did the author experience hypersensitivity while taking chlorhexidine gluconate?

What is this?

Tell us about your Experience with Chlorhexidine Gluconate Related Hypersensitivity

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: Hypersomnia, Hypoaesthesia, Hypersensitivity, Paraesthesia

Posted By Anonymous in askapatient.com on August 31, 2010 @ 12:00 am

Side Effects: I had numbness and tingling on the tip of my tongue after only two uses; this was similar to the 'pins & needles' sensation of a limb that falls asleep. This alarmed me and caused me to...

Druginformer Identified Side Effects: Erythema, Pruritus, Hypersensitivity, Urticaria, Rash

Posted By LJDunlap in fdb.rxlist.com on April 23, 2010 @ 12:00 am

... under the brand name Chloraprep was used on my skin prior to a surgical procedure to prevent infection. I've had a severe allergic reaction to it, with hives, rash, itching, redness, etc. covering the...



* 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.