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Nortriptyline Hydrochloride Related Dysgeusia

Official FDA Reports56
Social Media Events4
Active Ingredients
  • Nortriptyline Hydrochloride
Additional Terms for Dysgeusia
  • Bad Taste In Mouth
  • Bitter Taste
  • Altered Taste
  • Food Tasted A Bit Different
  • Changes In Taste
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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 Nortriptyline.


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

Nortriptyline Hydrochloride

Side Effects: So far all the side effects seem temporary. Cold hands/feet, white face. Bad taste in mouth . Fuzzy in the beginning. Nothing serious so far.

Mood lifted considerably. Ab...


Source:" Nortriptyline

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Did the author experience dysgeusia while taking nortriptyline hydrochloride?

What is this?

Nortriptyline Hydrochloride

Side Effects: Dry mouth, bad tast in mouth , difficulty sleeping, vivid dreams, hot flushes, hard to get motivated, hearing effected.


Source:" viewrating.asp

View full report on drug related dysgeusia

Did the author experience dysgeusia while taking nortriptyline hydrochloride?

What is this?

Nortriptyline Hydrochloride

Side Effects: Sleeping difficulties, nasty taste in mouth, vomiting, blurred vision, somnolence and insomnia. Strange dreams when I do sleep, and bouts of depression worse than normal.

Star...


Source:" viewrating.asp

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Did the author experience dysgeusia while taking nortriptyline hydrochloride?

What is this?

Tell us about your Experience with Nortriptyline Hydrochloride Related Dysgeusia

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Share Your Experience

Druginformer Identified Side Effects: Abnormal dreams, Dry mouth, Dysgeusia, Insomnia, Hot flush

Posted By Anonymous in askapatient.com on January 21, 2013 @ 12:00 am

Side Effects: Dry mouth, bad tast in mouth, difficulty sleeping, vivid dreams, hot flushes, hard to get motivated, hearing effected.

Druginformer Identified Side Effects: Vomiting, Abnormal dreams, Depression, Dysgeusia, Insomnia, Somnolence, Vision blurred

Posted By Anonymous in askapatient.com on August 6, 2012 @ 12:00 am

Side Effects: Sleeping difficulties, nasty taste in mouth, vomiting, blurred vision, somnolence and insomnia. Strange dreams when I do sleep, and bouts of depression worse than normal. Star...

Druginformer Identified Side Effects: Constipation, Dizziness, Dry skin, Dysgeusia

Posted By Anonymous in askapatient.com on October 13, 2004 @ 12:00 am

Mostly constipation and mouth dryness with bad taste. A few occasions of dizziness when standing up. At 50 mg was improving my mood a bit, but didn't like side effects, a...

Druginformer Identified Side Effects: Confusional state, Dysgeusia, Peripheral coldness, Skin hyperpigmentation

Posted By Anonymous in druglib.com

Side Effects: So far all the side effects seem temporary. Cold hands/feet, white face. Bad taste in mouth. Fuzzy in the beginning. Nothing serious so far. Mood lifted considerably. Ab...



* 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.