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Naproxen Sodium Related Myocardial Infarction

Official FDA Reports326
Social Media Events3

  This report is for all products sharing this active ingredient. For more details, please use our Workbench for research on individual brands like Aleve.


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

Aleve

Side Effects: Took 1 aleve for a headache and couldn't sleep. Started iching and feeling dizzy. Started to feel very nauscous and couldn't breath. I knew wasn't a heart attack but knew I was about to...


Source:" ALEVE: Side effects, ratings, and pati...

View full report on drug related myocardial infarction

Did the author experience myocardial infarction while taking aleve?

What is this?

Aleve

Side Effects: INSTANT ITCHING,SWEATING, THROAT CLOSURE ENDED UPIN ER THEY THOUGHT I WAS HAVING A HEART ATTACK BLOOD PRESSURE DROPPED TO 79/49 JUST GOT A BILL FOR 4600.00 FOR OVER NIGHT HOSPITAL VSIT ...


Source:" ALEVE: Side effects, ratings, and pati...

View full report on drug related myocardial infarction

Did the author experience myocardial infarction while taking aleve?

What is this?

Aleve

Side Effects: My grandfather took Aleve for about 6-12 months. He ended up with bleeding ulcers and a ruptured vein. He died on the operating table of a massive heart attack which according to the ...


Source:" ALEVE: Side effects, ratings, and pati...

View full report on drug related myocardial infarction

Did the author experience myocardial infarction while taking aleve?

What is this?

Tell us about your Experience with Naproxen Sodium Related Myocardial Infarction

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Share Your Experience

Druginformer Identified Side Effects: Dizziness, Pruritus, Loss of consciousness, Myocardial infarction, Insomnia, Respiration abnormal

Posted By Anonymous in askapatient.com on October 11, 2011 @ 12:00 am

Side Effects: Took 1 aleve for a headache and couldn't sleep. Started iching and feeling dizzy. Started to feel very nauscous and couldn't breath. I knew wasn't a heart attack but knew I was about to...

Druginformer Identified Side Effects: Pruritus, Myocardial infarction, Hyperhidrosis, Blood pressure abnormal

Posted By Anonymous in askapatient.com on December 6, 2006 @ 12:00 am

Side Effects: INSTANT ITCHING,SWEATING, THROAT CLOSURE ENDED UPIN ER THEY THOUGHT I WAS HAVING A HEART ATTACK BLOOD PRESSURE DROPPED TO 79/49 JUST GOT A BILL FOR 4600.00 FOR OVER NIGHT HOSPITAL VSIT ...

Druginformer Identified Side Effects: Myocardial infarction, Ulcer, Sudden death, Haemorrhage

Posted By Anonymous in askapatient.com on December 20, 2004 @ 12:00 am

Side Effects: My grandfather took Aleve for about 6-12 months. He ended up with bleeding ulcers and a ruptured vein. He died on the operating table of a massive heart attack which according to the ...



* 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.