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Chlorhexidine Gluconate Related Swelling

Official FDA Reports75
Social Media Events5

  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...

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Peridex

Side Effects: After one week my teeth have a brownish stain. It has impaired my sense of taste as well, but not completely lost.

It has stopped the red swelling and bleeding. I will find ou...


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

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Peridex

Side Effects: Unknowingly rinsed with it after cleaning at dentist thinking it was more mouthwash...intense bitterness and loss of taste immediately. Have swelling in neck, fullness in ears and woke...


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

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Tell us about your Experience with Chlorhexidine Gluconate Related Swelling

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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: Swelling

Posted By Anonymous in askapatient.com on October 29, 2010 @ 12:00 am

Side Effects: After one week my teeth have a brownish stain. It has impaired my sense of taste as well, but not completely lost. It has stopped the red swelling and bleeding. I will find ou...

Druginformer Identified Side Effects: Ageusia, Photophobia, Vertigo, Sensory loss, Swelling

Posted By Anonymous in askapatient.com on January 13, 2010 @ 12:00 am

Side Effects: Unknowingly rinsed with it after cleaning at dentist thinking it was more mouthwash...intense bitterness and loss of taste immediately. Have swelling in neck, fullness in ears and woke...

Druginformer Identified Side Effects: Burning sensation, Swelling, Tenderness

Posted By Anonymous in askapatient.com on August 31, 2006 @ 12:00 am

swelling of lips, face and tongue, alteration in taste, coated tongue, inflamatiom of salivary gland, soreness and burning pain on lining of cheeks and tongue -----unbearable

Druginformer Identified Side Effects: Pain, Burning sensation, Hypoaesthesia, Discomfort, Oedema, Paraesthesia, Swelling, Haemorrhage, Oral discomfort

Posted By Anonymous in askapatient.com on February 21, 2006 @ 12:00 am

Side Effects: numbness, burning, aching and swollen salivary glands, swelling of tongue, constant oral discomfort, constant tingling sensation on tongue and roof of mouth, increasing sense of impendi...



* 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.