Does FORMOTEROL\GLYCOPYRROLATE Cause Device issue? 139 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 139 reports of Device issue have been filed in association with FORMOTEROL\GLYCOPYRROLATE. This represents 9.3% of all adverse event reports for FORMOTEROL\GLYCOPYRROLATE.
139
Reports of Device issue with FORMOTEROL\GLYCOPYRROLATE
9.3%
of all FORMOTEROL\GLYCOPYRROLATE reports
0
Deaths
15
Hospitalizations
How Dangerous Is Device issue From FORMOTEROL\GLYCOPYRROLATE?
Of the 139 reports, 15 (10.8%) required hospitalization.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FORMOTEROL\GLYCOPYRROLATE. However, 139 reports have been filed with the FAERS database.
What Other Side Effects Does FORMOTEROL\GLYCOPYRROLATE Cause?
Dyspnoea (302)
Death (231)
Device malfunction (145)
Wrong technique in device usage process (139)
Off label use (134)
Cough (129)
Chronic obstructive pulmonary disease (125)
Intentional product misuse (115)
Intentional device misuse (103)
Wrong technique in product usage process (101)
What Other Drugs Cause Device issue?
ADALIMUMAB (17,630)
SOMATROPIN (5,131)
PEGFILGRASTIM (5,071)
ETANERCEPT (4,143)
INSULIN GLARGINE (3,175)
EXENATIDE (2,862)
LEVONORGESTREL (2,623)
CARBIDOPA\LEVODOPA (2,574)
GOLIMUMAB (1,827)
USTEKINUMAB (1,716)
Which FORMOTEROL\GLYCOPYRROLATE Alternatives Have Lower Device issue Risk?
FORMOTEROL\GLYCOPYRROLATE vs FORMOTEROL\MOMETASONE
FORMOTEROL\GLYCOPYRROLATE vs FORMOTEROL\MOMETASONE FUROATE
FORMOTEROL\GLYCOPYRROLATE vs FORTEO
FORMOTEROL\GLYCOPYRROLATE vs FOSAMAX
FORMOTEROL\GLYCOPYRROLATE vs FOSAMAX PLUS D