Does MOMETASONE FUROATE Cause Product quality issue? 3,406 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 3,406 reports of Product quality issue have been filed in association with MOMETASONE FUROATE (Mometasone Furoate). This represents 29.3% of all adverse event reports for MOMETASONE FUROATE.
3,406
Reports of Product quality issue with MOMETASONE FUROATE
29.3%
of all MOMETASONE FUROATE reports
2
Deaths
33
Hospitalizations
How Dangerous Is Product quality issue From MOMETASONE FUROATE?
Of the 3,406 reports, 2 (0.1%) resulted in death, 33 (1.0%) required hospitalization, and 3 (0.1%) were considered life-threatening.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MOMETASONE FUROATE. However, 3,406 reports have been filed with the FAERS database.
What Other Side Effects Does MOMETASONE FUROATE Cause?
No adverse event (3,717)
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)
Drug ineffective (935)
What Other Drugs Cause Product quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
METHYLPHENIDATE (1,728)
Which MOMETASONE FUROATE Alternatives Have Lower Product quality issue Risk?
MOMETASONE FUROATE vs MOMETASONE FUROATE\OLOPATADINE
MOMETASONE FUROATE vs MONOMETHYL
MOMETASONE FUROATE vs MONTELUKAST
MOMETASONE FUROATE vs MONTELUKAST\MONTELUKAST
MOMETASONE FUROATE vs MONTMORILLONITE