Does ULMUS AMERICANA POLLEN Cause Dyspnoea? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Dyspnoea have been filed in association with ULMUS AMERICANA POLLEN (CENTER-AL - ULMUS AMERICANA POLLEN). This represents 9.1% of all adverse event reports for ULMUS AMERICANA POLLEN.
6
Reports of Dyspnoea with ULMUS AMERICANA POLLEN
9.1%
of all ULMUS AMERICANA POLLEN reports
0
Deaths
2
Hospitalizations
How Dangerous Is Dyspnoea From ULMUS AMERICANA POLLEN?
Of the 6 reports, 2 (33.3%) required hospitalization.
Is Dyspnoea Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ULMUS AMERICANA POLLEN. However, 6 reports have been filed with the FAERS database.
What Other Side Effects Does ULMUS AMERICANA POLLEN Cause?
Anaphylactic reaction (19)
Injection site erythema (10)
Local reaction (9)
Urticaria (9)
Chest discomfort (7)
Injection site reaction (7)
Rash (7)
Pruritus (6)
False negative investigation result (5)
Injection site swelling (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)