AdverseEvent.ai
This page presents data from the FDA Adverse Event Reporting System (FAERS) and the FDA-approved drug label. A report submitted to FAERS does not prove a drug caused the reported event. Always consult a healthcare provider about medications.

Naproxen Sodium 220mg (naproxen sodium)

Last updated: June 21, 2026
Preview tracking

Naproxen Sodium 220mg is the brand name for naproxen sodium. According to the FDA-approved label, temporarily relieves minor aches and pains due to: minor pain of arthritis muscular aches backache menstrual cramps headache toothache the common cold temporarily reduces fever. FAERS contains 140,405 submissions naming this drug from 1998 through 2026; the top three reactions cited are drug ineffective, pain, and fatigue.

Most-Reported Reactions

Counts of the reactions most often cited in FAERS submissions that named Naproxen Sodium 220mg. Inclusion here does not establish causation - submitters describe what was observed, not what was confirmed. One submission can list several reactions, so the totals exceed the report count.

DRUG INEFFECTIVE 19,996 (14.2%) PAIN 12,287 (8.8%) FATIGUE 11,398 (8.1%) NAUSEA 10,568 (7.5%) ARTHRALGIA 10,354 (7.4%) HEADACHE 9,093 (6.5%) OFF LABEL USE 8,723 (6.2%) DIARRHOEA 8,373 (6.0%) DIZZINESS 7,835 (5.6%) VOMITING 7,342 (5.2%) RASH 7,116 (5.1%) DYSPNOEA 6,985 (5.0%) MALAISE 6,509 (4.6%) PAIN IN EXTREMITY 6,278 (4.5%) PRODUCT USE ISSUE 6,099 (4.3%)

Patient Demographics

Patient sex and age across the FAERS submissions that named Naproxen Sodium 220mg. Percentages here are computed only from submissions where these fields were filled in - many leave them blank.

By Sex

Female Male Unknown

By Age Group

0-17 18-44 45-64 65+

Severity Outcomes

Severity flags recorded across the 140,405 FAERS submissions that named Naproxen Sodium 220mg. Each bar shows the count of those reports carrying that flag. A single case can carry more than one (a hospitalization that became life-threatening, for example), so these bars are independent rates - they don't sum to 100%. Inclusion of a case under any flag does not establish that the drug caused the outcome.

DEATH 11,112 (7.9%) HOSPITALIZATION 35,564 (25.3%) LIFE-THREATENING 8,561 (6.1%) DISABLING 8,596 (6.1%)

Submissions Per Quarter

Quarterly count of FAERS submissions that named Naproxen Sodium 220mg. Ups and downs on this chart can track prescribing volume, news cycles, or shifts in how reports get filed, rather than the drug becoming safer or more dangerous.

1998 2002 2003 2004 2005 2006 2007 2008 2009 2010 2011 2012 2013 2014 2015 2016 2017 2018 2019 2020 2021 2022 2023 2024 2025 2026

From the FDA-Approved Label

Excerpts from the official FDA-approved prescribing information for Naproxen Sodium 220mg. This is the authoritative source on indications, warnings, and known adverse reactions.

Indications

temporarily relieves minor aches and pains due to: minor pain of arthritis muscular aches backache menstrual cramps headache toothache the common cold temporarily reduces fever

Warnings

Allergy alert: Naproxen sodium may cause a severe allergic reaction, especially in people allergic to aspirin. Symptoms may include hives facial swelling asthma (wheezing) shock skin reddening rash blisters If an allergic reaction occurs, stop use and seek medical help right away. Stomach bleeding warning: This product contains an NSAID, which may cause severe stomach bleeding. The chance is higher if you are age 60 or older have had stomach ulcers or bleeding problems take a blood thinning (anticoagulant) or steroid drug take other drugs containing prescription or nonprescription NSAIDs (aspirin, ibuprofen, naproxen, or others) have 3 or more alcoholic drinks every day while using this product take more or for a longer time than directed. Heart attack and stroke warning: NSAIDs, except aspirin, increase the risk of heart attack, heart failure, and stroke. These can be fatal. The risk is higher if you use more than directed or for longer than directed. Do not use if you have ever had an allergic reaction to any other pain reliever/fever reducer right before or after heart surgery Ask a doctor before use if the stomach bleeding warning applies to you you have a history of stomach pr...

FDA label effective date: 2018-12-14

Disclaimer

AdverseEvent.ai is not affiliated with the FDA. Adverse-event counts come from the FDA Adverse Event Reporting System (FAERS). Drug labels come from the FDA drug label dataset. A report submitted to FAERS does not prove a drug caused the reported event — always consult a healthcare provider about medications. This site is for informational purposes only and is not medical advice.