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Aleve Related Blindness

Official Government Database Reports30
Online Conversations3

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: Blindness, Sudden death, Fluid retention, Hypertension

Posted By Anonymous in askapatient.com on March 20, 2014 @ 12:00 am

... Worked for quite awhile for my foot injury, but it must have reached the tipping point because I almost died. Water retention led to extremely high blood pressure (260/110), vision loss in right eye f...

Druginformer Identified Side Effects: Headache, Dizziness, Blindness, Anxiety

Posted By Anonymous in askapatient.com on December 18, 2012 @ 12:00 am

Side Effects: Took one Aleve after breakfast, was OK until after lunch when a blinding headache hit, became dizzy and frightened. Had tried taking one Aleve several months ago. Same experience but ...

Druginformer Identified Side Effects: Nausea, Syncope, Vomiting, Blindness, Tinnitus, Hyperhidrosis

Posted By Anonymous in askapatient.com on October 11, 2006 @ 12:00 am

Side Effects: Took 2 aleve for a headache and 15 minutes later experienced nausea, vomiting, diarehea, pouring sweat, ringing in ears, loss of vision, fainting, and closing of throat.. in other words...

* 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.