Does UMECLIDINIUM Cause Intercepted product administration error? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Intercepted product administration error have been filed in association with UMECLIDINIUM (Anoro Ellipta). This represents 0.1% of all adverse event reports for UMECLIDINIUM.
7
Reports of Intercepted product administration error with UMECLIDINIUM
0.1%
of all UMECLIDINIUM reports
0
Deaths
0
Hospitalizations
How Dangerous Is Intercepted product administration error From UMECLIDINIUM?
Of the 7 reports.
Is Intercepted product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for UMECLIDINIUM. However, 7 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 Intercepted product administration error?
EVOLOCUMAB (2,508)
DENOSUMAB (1,209)
ERENUMAB-AOOE (1,015)
ETANERCEPT (574)
DARBEPOETIN ALFA (385)
PEGFILGRASTIM (356)
LEUPROLIDE (307)
ERYTHROPOIETIN (301)
ROMOSOZUMAB-AQQG (115)
BENZYL ALCOHOL\ETANERCEPT (112)
Which UMECLIDINIUM Alternatives Have Lower Intercepted product administration error Risk?
UMECLIDINIUM vs UMECLIDINIUM\VILANTEROL TRIFENATATE
UMECLIDINIUM vs UMIFENOVIR
UMECLIDINIUM vs UNSPECIFIED INGREDIENT
UMECLIDINIUM vs UPADACITINIB
UMECLIDINIUM vs URAPIDIL