DrugInformer Search

Doxepin Hydrochloride Related Gait Disturbance

Official FDA Reports100
Social Media Events3
Active Ingredients
  • Doxepin Hydrochloride
Additional Terms for Gait Disturbance
  • Unsteady Gait
  • Loss Of Balance
  • Walking Compromised
  • Cab Hardly Walk
  • Very Unstable And Could Not Walk Without Help
Show more

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


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

Doxepin Hydrochloride

Side Effects: Stiffness and pain so bad I could hardly walk .

Like another patient, I took this a few years ago with no bad side effects. Then was off of it for a while. Started back on it a...


Source:" viewrating.asp

View full report on drug related gait disturbance

Did the author experience gait disturbance while taking doxepin hydrochloride?

What is this?

Doxepin Hydrochloride

Side Effects: I took this drug for quit awhile 3-4 yrs ago with no side effect. Now I started taking again with terrible side effects. Worst my legs ache so bad it is hard to walk . They ache so bad a...


Source:" viewrating.asp

View full report on drug related gait disturbance

Did the author experience gait disturbance while taking doxepin hydrochloride?

What is this?

Sinequan

Side Effects: buzzing feeling, didnt wake up til 1045 the next day..took 24hrs to sleep it off. unbalanced and felt drunk...just awful


Source:" viewrating.asp

View full report on drug related gait disturbance

Did the author experience gait disturbance while taking sinequan?

What is this?

Tell us about your Experience with Doxepin Hydrochloride Related Gait Disturbance

Thank you for sharing your experience with us!

Share Your Experience

Druginformer Identified Side Effects: Gait disturbance, Joint stiffness

Posted By Anonymous in askapatient.com on May 30, 2014 @ 12:00 am

Side Effects: Stiffness and pain so bad I could hardly walk. Like another patient, I took this a few years ago with no bad side effects. Then was off of it for a while. Started back on it a...

Druginformer Identified Side Effects: Headache, Fatigue, Drug effect increased, Gait disturbance, Tenderness

Posted By Anonymous in askapatient.com on December 2, 2013 @ 12:00 am

... Now I started taking again with terrible side effects. Worst my legs ache so bad it is hard to walk. They ache so bad at night so sleep. I have been bitchy, tired, sore, headaches but the worst are my...

Druginformer Identified Side Effects: Feeling drunk, Gait disturbance

Posted By Anonymous in askapatient.com on September 16, 2003 @ 12:00 am

Side Effects: buzzing feeling, didnt wake up til 1045 the next day..took 24hrs to sleep it off. unbalanced and felt drunk...just awful



* 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.