Does UMECLIDINIUM Cause Gastrooesophageal reflux disease? 304 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 304 reports of Gastrooesophageal reflux disease have been filed in association with UMECLIDINIUM (Anoro Ellipta). This represents 4.8% of all adverse event reports for UMECLIDINIUM.
304
Reports of Gastrooesophageal reflux disease with UMECLIDINIUM
4.8%
of all UMECLIDINIUM reports
9
Deaths
188
Hospitalizations
How Dangerous Is Gastrooesophageal reflux disease From UMECLIDINIUM?
Of the 304 reports, 9 (3.0%) resulted in death, 188 (61.8%) required hospitalization, and 63 (20.7%) were considered life-threatening.
Is Gastrooesophageal reflux disease Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for UMECLIDINIUM. However, 304 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 Gastrooesophageal reflux disease?
ESOMEPRAZOLE (4,746)
OMEPRAZOLE (3,929)
PANTOPRAZOLE (3,456)
PREDNISONE (2,797)
LANSOPRAZOLE (2,482)
ADALIMUMAB (2,450)
ALENDRONATE (2,046)
ALBUTEROL (2,019)
OLMESARTAN MEDOXOMIL (1,819)
METHOTREXATE (1,757)
Which UMECLIDINIUM Alternatives Have Lower Gastrooesophageal reflux disease Risk?
UMECLIDINIUM vs UMECLIDINIUM\VILANTEROL TRIFENATATE
UMECLIDINIUM vs UMIFENOVIR
UMECLIDINIUM vs UNSPECIFIED INGREDIENT
UMECLIDINIUM vs UPADACITINIB
UMECLIDINIUM vs URAPIDIL