Naproxen Sodium

Average User Review Score

* Based on 6 reviews from across the web.

Wikipedia

Naproxen /nəˈprɒksən/ (INN; brand names: Aleve, Naprosyn and many others) is a nonselective COX inhibitor; usually sold as the sodium salt, naproxen is a nonsteroidal anti-inflammatory drug (NSAID) of the propionic acid class (which puts it in the same class as ibuprofen) commonly used for relief of a wide variety of pain, fever, swelling and stiffness.

Common adverse events from online conversations

Common adverse events from FDA database

* Extracted from FDA Adverse Event Reports for all drugs with the same active ingredients.

Tell us about your Experience with Naproxen Sodium

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Druginformer Identified Side Effects: None

Posted By kirby in drugs.com on September 4, 2004 @ 12:00 am

“Joanna is correct. Blue oval pill imprinted L 368 is 220 mg naproxen sodium sold over the counter.”

Druginformer Identified Side Effects: None

Posted By kirby in drugs.com on July 21, 2004 @ 12:00 am

“According to one database, blue oval G17 is 220 mg naproxen sodium. I can't confirm the info with other sources, but I think it's accurate since a blue round tablet imprinted with G14 is 220 mg...”

Druginformer Identified Side Effects: None

Posted By Sue9C in drugs.com on July 10, 2004 @ 12:00 am

“I have very bad allergies and Naproxen Sodium has worked wonders for me. Susan Cherry”

Druginformer Identified Side Effects: None

Posted By Anonymous in ehealthforum.com

“Is it safe to take naproxen sodium and acetominophen at the same time or should the times be staggered? Thanks!”

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* 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.