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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does NAPROXEN 16028/0144 Cause Dyspnoea? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Dyspnoea have been filed in association with NAPROXEN 16028/0144. This represents 12.8% of all adverse event reports for NAPROXEN 16028/0144.

5
Reports of Dyspnoea with NAPROXEN 16028/0144
12.8%
of all NAPROXEN 16028/0144 reports
0
Deaths
2
Hospitalizations

How Dangerous Is Dyspnoea From NAPROXEN 16028/0144?

Of the 5 reports, 2 (40.0%) required hospitalization.

Is Dyspnoea Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for NAPROXEN 16028/0144. However, 5 reports have been filed with the FAERS database.

What Other Side Effects Does NAPROXEN 16028/0144 Cause?

What Other Drugs Cause Dyspnoea?

ALBUTEROL (21,856) TREPROSTINIL (16,348) AMBRISENTAN (13,367) PREDNISONE (12,830) BUDESONIDE\FORMOTEROL (11,158) TIOTROPIUM (10,863) ADALIMUMAB (10,547) DUPILUMAB (10,310) FLUTICASONE\SALMETEROL (9,783) MEPOLIZUMAB (9,192)

Related Pages

NAPROXEN 16028/0144 Full Profile All Dyspnoea Reports All Drugs Causing Dyspnoea NAPROXEN 16028/0144 Demographics