Does MOMETASONE FUROATE Cause Device use error? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Device use error have been filed in association with MOMETASONE FUROATE (Mometasone Furoate). This represents 0.0% of all adverse event reports for MOMETASONE FUROATE.
5
Reports of Device use error with MOMETASONE FUROATE
0.0%
of all MOMETASONE FUROATE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Device use error From MOMETASONE FUROATE?
Of the 5 reports.
Is Device use error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MOMETASONE FUROATE. However, 5 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 use error?
PEGFILGRASTIM (6,001)
ALBUTEROL (5,215)
ALBIGLUTIDE (4,056)
EVOLOCUMAB (4,002)
SOMATROPIN (2,801)
FLUTICASONE\SALMETEROL (1,749)
FLUTICASONE (783)
FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (766)
ERENUMAB-AOOE (711)
ETANERCEPT (665)
Which MOMETASONE FUROATE Alternatives Have Lower Device use error Risk?
MOMETASONE FUROATE vs MOMETASONE FUROATE\OLOPATADINE
MOMETASONE FUROATE vs MONOMETHYL
MOMETASONE FUROATE vs MONTELUKAST
MOMETASONE FUROATE vs MONTELUKAST\MONTELUKAST
MOMETASONE FUROATE vs MONTMORILLONITE