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Naproxen Sodium Related Anaphylactic Shock

Official FDA Reports136
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: Genitals and feet began burning and itching. Began to have trouble breathing and went into anaphylactic shock . Passed out before paramedics arrived. Blood pressure could not be measured...


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

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Did the author experience anaphylactic shock while taking aleve?

What is this?

Aleve

... ER, given Benedryl. Told not to take any other related drugs: ibuprofen, asprin, naproxin. Once you have a reaction, subsequent reactions will get worse and worse to the point of anaphylactic shock ....


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

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Did the author experience anaphylactic shock while taking aleve?

What is this?

Aleve

... 24 hours, I had a slight relapse and ended up back in the emergency room. Although the ER termed this severe allergic reaction, my symptoms were identical to a case of anaphylactic shock I had a doze...


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

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Tell us about your Experience with Naproxen Sodium Related Anaphylactic Shock

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Share Your Experience

Druginformer Identified Side Effects: Anaphylactic shock, Loss of consciousness, Pruritus, Burning sensation, Dyspnoea

Posted By Anonymous in askapatient.com on February 21, 2015 @ 12:00 am

Side Effects: Genitals and feet began burning and itching. Began to have trouble breathing and went into anaphylactic shock. Passed out before paramedics arrived. Blood pressure could not be measured...

Druginformer Identified Side Effects: Pruritus, Anaphylactic shock, Palpitations, Rash, Swelling, Tachypnoea

Posted By Anonymous in askapatient.com on December 21, 2010 @ 12:00 am

Side Effects: Swelling of the hands, itching, red rash covering torso, hands and face. Elevated heart rate shallow rapid breathing. Went to ER, given Benedryl. Told not to take any other r...

Druginformer Identified Side Effects: Dizziness, Pain, Pruritus, Dry skin, Burning sensation, Hypersensitivity, Anaphylactic shock, Swelling

Posted By Anonymous in askapatient.com on August 21, 2007 @ 12:00 am

... B.M.'s. At that time, I began turning red and swell all over. Every part of me itched. Even my face felt like it was on fire. My throat was dry and chest was hurting. I felt faint. Rescue squad...



* 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.