Does POA PRATENSIS POLLEN 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 POA PRATENSIS POLLEN (Kentucky Bluegrass (June) Standardized). This represents 15.6% of all adverse event reports for POA PRATENSIS POLLEN.
5
Reports of Dyspnoea with POA PRATENSIS POLLEN
15.6%
of all POA PRATENSIS POLLEN reports
0
Deaths
1
Hospitalizations
How Dangerous Is Dyspnoea From POA PRATENSIS POLLEN?
Of the 5 reports, 1 (20.0%) required hospitalization, and 1 (20.0%) were considered life-threatening.
Is Dyspnoea Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for POA PRATENSIS POLLEN. However, 5 reports have been filed with the FAERS database.
What Other Side Effects Does POA PRATENSIS POLLEN Cause?
Cough (9)
Anaphylactic reaction (8)
Throat irritation (8)
False negative investigation result (5)
Rhinorrhoea (5)
Swelling face (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)