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Modafinil Related Incontinence

Official FDA Reports26
Social Media Events3
Active Ingredients
  • Modafinil
Additional Drug Brands and Names
Additional Terms for Incontinence
  • Unable To Control My Bladder
  • Loss Bladder Control
  • Loss Of Bladder/bowel Control
  • Bladder Was Leaking
  • Loss Of Bladder Control
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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 Provigil.


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

Provigil

... was sleeping for at least 9 hours plus at least 2- 3 hrs of napping. I have taken dexadrine and adderall, both of which had annoying side effects: increased urgency to urinate , sweating (bad!), dry an...


Source:" Provigil Oral : User Ratings covering ...

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Did the author experience incontinence while taking provigil?

What is this?

Provigil

... by the way). I've been on it for 4 days .Now I have a horrible headache (used to get these and migraines and hadn't had one for years until now). I also have severe incontinence , which I haven't had w...


Source:" Nuvigil Side Effects

View full report on drug related incontinence

Did the author experience incontinence while taking provigil?

What is this?

Provigil

... like symptoms. My speech was impaired for 6 months. I had seizures they just disregarded it as that. I had to learn to walk for a week. It has never happened before. I have incontinence problems. I am...


Source:" Usage Ms

View full report on drug related incontinence

Did the author experience incontinence while taking provigil?

What is this?

Tell us about your Experience with Modafinil Related Incontinence

Thank you for sharing your experience with us!

Share Your Experience

Druginformer Identified Side Effects: Dry skin, Drug ineffective, Hyperhidrosis, Incontinence

Posted By Anonymous in fdb.rxlist.com on February 29, 2008 @ 12:00 am

I was prescribed provigil for chronic fatigue and difficulty concentrating. I was always really tired during the day, did not have sleep apnea or any other health problems and was sleeping for at leas...

Druginformer Identified Side Effects: Headache, Incontinence

Posted By Troubled By This in prescriptiondrug-info.com on February 1, 2011 @ 12:00 am

... pharmacy management company wouldn't allow me to continue with the Provigil I've taken for years (that works, by the way). I've been on it for 4 days .Now I have a horrible headache (used to get these...

Druginformer Identified Side Effects: Adverse event, Incontinence

Posted By kathlene in prescriptiondrug-info.com on November 12, 2008 @ 12:00 am

I use provigil for narcolepsy but have a question about whether or not I have MS. IAbout 8 months ago I was put in the hosp. due to stroke like symptoms. My speech was impaired for 6 months. I had sei...



* 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.