Does MOMETASONE FUROATE\OLOPATADINE Cause Device issue? 43 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 43 reports of Device issue have been filed in association with MOMETASONE FUROATE\OLOPATADINE. This represents 4.3% of all adverse event reports for MOMETASONE FUROATE\OLOPATADINE.
43
Reports of Device issue with MOMETASONE FUROATE\OLOPATADINE
4.3%
of all MOMETASONE FUROATE\OLOPATADINE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Device issue From MOMETASONE FUROATE\OLOPATADINE?
Of the 43 reports.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MOMETASONE FUROATE\OLOPATADINE. However, 43 reports have been filed with the FAERS database.
What Other Side Effects Does MOMETASONE FUROATE\OLOPATADINE Cause?
Device delivery system issue (347)
Product use in unapproved indication (318)
Drug dose omission by device (274)
Product use issue (228)
Drug ineffective (98)
Epistaxis (78)
Wrong technique in device usage process (70)
Device occlusion (54)
Wrong technique in product usage process (47)
Product delivery mechanism issue (45)
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 MOMETASONE FUROATE\OLOPATADINE Alternatives Have Lower Device issue Risk?
MOMETASONE FUROATE\OLOPATADINE vs MONOMETHYL
MOMETASONE FUROATE\OLOPATADINE vs MONTELUKAST
MOMETASONE FUROATE\OLOPATADINE vs MONTELUKAST\MONTELUKAST
MOMETASONE FUROATE\OLOPATADINE vs MONTMORILLONITE
MOMETASONE FUROATE\OLOPATADINE vs MORNIFLUMATE