This report is for all products sharing this active ingredient. For more details, please use our Workbench for research on individual brands like Aleve.
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.
Report Date | Dosage | Indication | Outcome | Country | Gender | Age | Weight (lbs) |
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* DrugInformer calculates alarm using a proprietary algorithm. Alarm should not be taken as an ofiicial signal from the FDA or other regulatory entity.
Druginformer Identified Side Effects: Dizziness, Vomiting, Hypoaesthesia, Accidental poisoning, Muscular weakness, Paraesthesia, Peripheral coldness, Emotional distress, Abasia
Posted By Anonymous in askapatient.com on September 24, 2009 @ 12:00 am
“... Wow! I went home and slept and rested for the rest of day and night since I could not do much else. It has been three days since and still have weak and tired moments and some dizziness. I found this ...”
Druginformer Identified Side Effects: Loss of consciousness, Scar, Emotional distress, Chronic gastrointestinal bleeding
Posted By Anonymous in askapatient.com on April 15, 2007 @ 12:00 am
“Side Effects: After 7 days of taking Aleve (2 x per day) I had sudden, painless, massive GI bleeding; was rushed to the emergency room, passed out, more blood, code blue. I required 4 units of bloo...”
* 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.
Social Media Comments From Around the Web
The following are comments from users that experienced side effects while taking Milnacipran Hydrochloride
Aleve
“Side Effects: Severe illness, with vomiting, numb tingling feet and cold hands. Very weak could not walk without assitance. Became emotional at times(not like me). I thought I may die. I felt as if I...”
Source:" ALEVE: Side effects, ratings, and pati...
View full report on drug related emotional distress
Did the author experience emotional distress while taking aleve?
What is this?Aleve
“... to the emergency room, passed out, more blood, code blue. I required 4 units of blood transfusion. Fortunately I survived this near-death experience, but it has left some big emotional scars. I hav...”
Source:" ALEVE: Side effects, ratings, and pati...
View full report on drug related emotional distress
Did the author experience emotional distress while taking aleve?
What is this?