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Fenofibrate Related Neuropathy Peripheral

Official FDA Reports201
Social Media Events3
Active Ingredients
  • Fenofibrate
Additional Terms for Neuropathy Peripheral
  • Neuropathy
  • Neuropothy
  • Nuropathic Pain
  • Neuropathy/partial Numbness In Hands
  • Neruopathy

  This report is for all products sharing this active ingredient. For more details, please use our Workbench for research on individual brands like Tricor.


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

Tricor (micronized)

... I have been experiencing over the last few months. Okay, it's either Tricor or Lyrica, and that doesn't seem too possible since Lyrica is supposed to be "for" my muscle pain and neuropathy in my foot...


Source:" TRICOR (MICRONIZED): Side effects, rat...

View full report on drug related neuropathy peripheral

Did the author experience neuropathy peripheral while taking tricor (micronized)?

What is this?

Tricor (micronized)

... taking Tricor concomitantly with Lopid for nearly two years. Shortly thereafter I was led to believe my body was simply falling apart when the symptoms begin: Peripheral Neuropathy (numbness in the e...


Source:" TRICOR (MICRONIZED): Side effects, rat...

View full report on drug related neuropathy peripheral

Did the author experience neuropathy peripheral while taking tricor (micronized)?

What is this?

Tricor (micronized)

... imbalance. I called my internist and he order ed Tricor. After less than one day I have generalized joint and muscle pain. I have osteoarthritis and peripheral neuropathy from diabetes. This new p...


Source:" TRICOR (MICRONIZED): Side effects, rat...

View full report on drug related neuropathy peripheral

Did the author experience neuropathy peripheral while taking tricor (micronized)?

What is this?

Tell us about your Experience with Fenofibrate Related Neuropathy Peripheral

Thank you for sharing your experience with us!

Share Your Experience

Druginformer Identified Side Effects: Arthralgia, Neuropathy peripheral, Herpes zoster

Posted By Anonymous in askapatient.com on April 1, 2010 @ 12:00 am

Side Effects: I have been having rather strong joint pain. I think I have come to the conclusion that Tricor has caused me this severe joint pain I have been experiencing over the last few ...

Druginformer Identified Side Effects: Arthralgia, Pain, Myalgia, Hypoaesthesia, Neuropathy peripheral, Carpal tunnel syndrome

Posted By Anonymous in askapatient.com on February 20, 2009 @ 12:00 am

... I was led to believe my body was simply falling apart when the symptoms begin: Peripheral Neuropathy (numbness in the extremities – hands, fingers and feet); severe joint pain; muscle pain and inabil...

Druginformer Identified Side Effects: Blood test, Balance disorder, Arthralgia, Myalgia, Diabetes, Neuropathy peripheral, Erectile dysfunction, Blood cholesterol increased, Osteoarthritis

Posted By Anonymous in askapatient.com on August 30, 2008 @ 12:00 am

... taking Crestor. My cardiologist was concerned when I told him I was experiencing muscle and joint pain. He ordered that I stop the Crestor immediately. My next blood test showed elevated cholestrol...



* 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.