DrugInformer Search

Provigil Related Joint stiffness

Official Government Database Reports25
Online Conversations4

Extracted from FDA Adverse Event Reports for all drugs with the same active ingredients. To view the active ingredient report, please click here.

Tell us about your Experience with Provigil

Thank you for sharing your experience with us!

Share Your Experience

Druginformer Identified Side Effects: Tremor, Eye pain, Tinnitus, Memory impairment, Obsessive-compulsive disorder, Amnesia, Condition aggravated, Disturbance in attention, Dry eye, Insomnia, Irritability, Joint stiffness, Loss of libido

Posted By Anonymous in askapatient.com on November 18, 2007 @ 12:00 am

Side Effects: severe ringing in ears, intermittent sharp/needle eye pain, stiff joints, very poor short term memory, zero sex drive, chewing inside mouth, more OCD, severe abdominal issues aggrevated...

Druginformer Identified Side Effects: Pain, Eye inflammation, Dry eye, Dry mouth, Joint stiffness, Vision blurred

Posted By Anonymous in askapatient.com on May 14, 2006 @ 12:00 am

... dosage from 200mg to 400mg for less than two weeks. back to 200mg for 2 months, just tried to increase dosage to 400mg again for less than a week, I start to feel pain behind the eyes. Hands/fingers w...

Druginformer Identified Side Effects: Chest pain, Sunburn, Joint stiffness

Posted By Anonymous in askapatient.com on April 29, 2005 @ 12:00 am

Side Effects: I notice that my neck seems more stiff then usual.I get chest pain in the evening, and my face feels like its been sunburned? I am not sure what to think. The Provigil has giv...

Druginformer Identified Side Effects: Joint stiffness, Insomnia

Posted By getting by in healingwell.com on December 5, 2009 @ 12:00 am

Sandi? Does hyperinsomnia mean that you sleep a lot? Because the provigil helps to keep you awake. I use to take it but I take adderall instead now. It keeps me awake during the day. Best wishes to...

* 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.