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Modafinil Related Headache

Official Government Database Reports89
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Extracted from FDA Adverse Event Reports for all drugs with the same active ingredients. To view the active ingredient report, please click here.

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Druginformer Identified Side Effects: Headache

Posted By 100000286519574 in facebook.com on May 8, 2013 @ 12:00 am

... to 200mg in a day. It wasn't difficult for me to get it prescribed. The first time I tried taking it I took 200mg a day for a week and noticed no benefits, just insomnia and headaches. My eyes felt as...

Druginformer Identified Side Effects: Headache, Nausea

Posted By Annie50 in www.dailystrength.org on January 1, 2009 @ 12:00 am

My son ( 21 ) is on Modafinil. When he first went on it he suffered with acute headaches and nausea. This lasted for a few weeks, but then it went away. He has been on this medication for just under a...

Druginformer Identified Side Effects: Headache, Vaginal haemorrhage

Posted By Tony in prescriptiondrug-info.com on November 21, 2005 @ 12:00 am

... fingers or ankles. CONTACT YOUR DOCTOR IMMEDIATELY if you experience calf/leg pain or swelling; trouble breathing or shortness of breath; chest pain; sudden severe headache, dizziness, or fainting; ab...

* 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.