Does FRAXINUS AMERICANA POLLEN Cause Dyspnoea? 10 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 10 reports of Dyspnoea have been filed in association with FRAXINUS AMERICANA POLLEN (CENTER-AL - FRAXINUS AMERICANA POLLEN). This represents 14.7% of all adverse event reports for FRAXINUS AMERICANA POLLEN.
10
Reports of Dyspnoea with FRAXINUS AMERICANA POLLEN
14.7%
of all FRAXINUS AMERICANA POLLEN reports
0
Deaths
2
Hospitalizations
How Dangerous Is Dyspnoea From FRAXINUS AMERICANA POLLEN?
Of the 10 reports, 2 (20.0%) required hospitalization.
Is Dyspnoea Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FRAXINUS AMERICANA POLLEN. However, 10 reports have been filed with the FAERS database.
What Other Side Effects Does FRAXINUS AMERICANA POLLEN Cause?
Anaphylactic reaction (22)
Injection site reaction (9)
Local reaction (9)
Injection site erythema (6)
Urticaria (6)
False negative investigation result (5)
Injection site urticaria (5)
Throat irritation (5)
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)