Does MOMETASONE FUROATE Cause Device dislocation? 92 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 92 reports of Device dislocation have been filed in association with MOMETASONE FUROATE (Mometasone Furoate). This represents 0.8% of all adverse event reports for MOMETASONE FUROATE.
92
Reports of Device dislocation with MOMETASONE FUROATE
0.8%
of all MOMETASONE FUROATE reports
0
Deaths
79
Hospitalizations
How Dangerous Is Device dislocation From MOMETASONE FUROATE?
Of the 92 reports, 79 (85.9%) required hospitalization, and 20 (21.7%) were considered life-threatening.
Is Device dislocation Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MOMETASONE FUROATE. However, 92 reports have been filed with the FAERS database.
What Other Side Effects Does MOMETASONE FUROATE Cause?
No adverse event (3,717)
Product quality issue (3,406)
Poor quality device used (2,159)
Drug dose omission (2,005)
Dyspnoea (1,522)
Device malfunction (1,332)
Asthma (1,307)
Wheezing (1,142)
Cough (1,052)
Gastrooesophageal reflux disease (1,029)
What Other Drugs Cause Device dislocation?
LEVONORGESTREL (13,757)
COPPER (6,955)
CARBIDOPA\LEVODOPA (2,937)
ETONOGESTREL (2,909)
TREPROSTINIL (1,626)
MIRENA (677)
BACLOFEN (492)
PARAGARD 380A (479)
ADALIMUMAB (372)
EPOPROSTENOL (358)
Which MOMETASONE FUROATE Alternatives Have Lower Device dislocation Risk?
MOMETASONE FUROATE vs MOMETASONE FUROATE\OLOPATADINE
MOMETASONE FUROATE vs MONOMETHYL
MOMETASONE FUROATE vs MONTELUKAST
MOMETASONE FUROATE vs MONTELUKAST\MONTELUKAST
MOMETASONE FUROATE vs MONTMORILLONITE