Does UMECLIDINIUM Cause Haemoptysis? 163 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 163 reports of Haemoptysis have been filed in association with UMECLIDINIUM (Anoro Ellipta). This represents 2.6% of all adverse event reports for UMECLIDINIUM.
163
Reports of Haemoptysis with UMECLIDINIUM
2.6%
of all UMECLIDINIUM reports
60
Deaths
104
Hospitalizations
How Dangerous Is Haemoptysis From UMECLIDINIUM?
Of the 163 reports, 60 (36.8%) resulted in death, 104 (63.8%) required hospitalization, and 152 (93.3%) were considered life-threatening.
Is Haemoptysis Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for UMECLIDINIUM. However, 163 reports have been filed with the FAERS database.
What Other Side Effects Does UMECLIDINIUM Cause?
Dyspnoea (1,817)
Asthma (1,433)
Wheezing (1,111)
Therapeutic product effect incomplete (980)
Cough (913)
Drug ineffective (734)
Loss of personal independence in daily activities (711)
Obstructive airways disorder (654)
Chronic obstructive pulmonary disease (588)
Condition aggravated (580)
What Other Drugs Cause Haemoptysis?
RIVAROXABAN (1,961)
ASPIRIN (1,255)
APIXABAN (846)
TREPROSTINIL (838)
ALBUTEROL (652)
CLOPIDOGREL BISULFATE (643)
PREDNISONE (618)
WARFARIN (555)
ADALIMUMAB (472)
TIOTROPIUM (462)
Which UMECLIDINIUM Alternatives Have Lower Haemoptysis Risk?
UMECLIDINIUM vs UMECLIDINIUM\VILANTEROL TRIFENATATE
UMECLIDINIUM vs UMIFENOVIR
UMECLIDINIUM vs UNSPECIFIED INGREDIENT
UMECLIDINIUM vs UPADACITINIB
UMECLIDINIUM vs URAPIDIL