Does UMECLIDINIUM Cause Incorrect product administration duration? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Incorrect product administration duration have been filed in association with UMECLIDINIUM (Anoro Ellipta). This represents 0.1% of all adverse event reports for UMECLIDINIUM.
5
Reports of Incorrect product administration duration with UMECLIDINIUM
0.1%
of all UMECLIDINIUM reports
0
Deaths
0
Hospitalizations
How Dangerous Is Incorrect product administration duration From UMECLIDINIUM?
Of the 5 reports.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for UMECLIDINIUM. However, 5 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 Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which UMECLIDINIUM Alternatives Have Lower Incorrect product administration duration Risk?
UMECLIDINIUM vs UMECLIDINIUM\VILANTEROL TRIFENATATE
UMECLIDINIUM vs UMIFENOVIR
UMECLIDINIUM vs UNSPECIFIED INGREDIENT
UMECLIDINIUM vs UPADACITINIB
UMECLIDINIUM vs URAPIDIL