Does MORUS RUBRA POLLEN Cause Dyspnoea? 11 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Dyspnoea have been filed in association with MORUS RUBRA POLLEN (CENTER-AL - MORUS RUBRA POLLEN). This represents 22.0% of all adverse event reports for MORUS RUBRA POLLEN.
11
Reports of Dyspnoea with MORUS RUBRA POLLEN
22.0%
of all MORUS RUBRA POLLEN reports
0
Deaths
1
Hospitalizations
How Dangerous Is Dyspnoea From MORUS RUBRA POLLEN?
Of the 11 reports, 1 (9.1%) required hospitalization.
Is Dyspnoea Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MORUS RUBRA POLLEN. However, 11 reports have been filed with the FAERS database.
What Other Side Effects Does MORUS RUBRA POLLEN Cause?
Anaphylactic reaction (12)
Cough (9)
Throat irritation (9)
Injection site reaction (7)
Pruritus (6)
Urticaria (6)
Dizziness (5)
Flushing (5)
Headache (5)
Injection site erythema (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)