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Modafinil Related Accidental Poisoning

Official FDA Reports0
Social Media Events3
Active Ingredients
  • Modafinil
Additional Drug Brands and Names
Additional Terms for Accidental Poisoning
  • Poisoned

  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

Modafinil

... got worse, no medicines helped with the headache. Then I started itching. At first I didn't connect it to the Provigil, then I broke out EVERYWHERE with a rash that was like poison ivy just worse. So ...


Source:" comments/modafinil/provigil.html&sa=U&...

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Did the author experience accidental poisoning while taking modafinil?

What is this?

Provigil

... defeated the entire purpose of taking the medication. I also had a terrible rash on my face (my eye almost swelled shut), neck, and arms. At the time I blamed the rash on possible poison ivy since I ...


Source:" PROVIGIL: Side effects, ratings, and p...

View full report on drug related accidental poisoning

Did the author experience accidental poisoning while taking provigil?

What is this?

Provigil

provigil I took this for one month and the only descriptive words I could find for how bad it made me feel were that I feel poisoned . Every cell of my body seemed to feel awful. Sorry to be so vague, ...


Source:" Provigil

View full report on drug related accidental poisoning

Did the author experience accidental poisoning while taking provigil?

What is this?

Tell us about your Experience with Modafinil Related Accidental Poisoning

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Share Your Experience

Druginformer Identified Side Effects: Headache, Fatigue, Pruritus, Accidental poisoning, Adverse drug reaction

Posted By Anonymous in drugs.com on May 2, 2010 @ 12:00 am

I was put on Provigil a year and a half ago and can no longer take it. I was one of the ones that had a horrible reaction to it. At first it was just a headache then I would crash around 5... the the ...

Druginformer Identified Side Effects: Alopecia, Accidental poisoning, Acne, Hyperhidrosis, Hypertension, Mania, Psychomotor hyperactivity, Rash, Weight decreased, Decreased appetite

Posted By Anonymous in askapatient.com on July 24, 2009 @ 12:00 am

Side Effects: RASH, loss of appetite, mania, over-medicated feeling, acne, thinning hair Like many others, the first time I took it was great! I had energy, hyper mental clarity, and a fee...

Druginformer Identified Side Effects: Accidental poisoning

Posted By Anonymous in everydayhealth.com on January 14, 2005 @ 12:00 am

provigil I took this for one month and the only descriptive words I could find for how bad it made me feel were that I feel poisoned. Every cell of my body seemed to feel awful. Sorry to be so vague, ...



* 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.