Does MOMETASONE FUROATE Cause Device malfunction? 1,332 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,332 reports of Device malfunction have been filed in association with MOMETASONE FUROATE (Mometasone Furoate). This represents 11.5% of all adverse event reports for MOMETASONE FUROATE.
1,332
Reports of Device malfunction with MOMETASONE FUROATE
11.5%
of all MOMETASONE FUROATE reports
0
Deaths
97
Hospitalizations
How Dangerous Is Device malfunction From MOMETASONE FUROATE?
Of the 1,332 reports, 97 (7.3%) required hospitalization, and 20 (1.5%) were considered life-threatening.
Is Device malfunction Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MOMETASONE FUROATE. However, 1,332 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)
Asthma (1,307)
Wheezing (1,142)
Cough (1,052)
Gastrooesophageal reflux disease (1,029)
Drug ineffective (935)
What Other Drugs Cause Device malfunction?
PEGFILGRASTIM (6,818)
EXENATIDE (3,273)
BUDESONIDE\FORMOTEROL (2,771)
ABATACEPT (2,459)
SOMATROPIN (2,311)
GOLIMUMAB (2,293)
SECUKINUMAB (2,259)
ALBUTEROL (2,257)
GUSELKUMAB (1,410)
ACLIDINIUM (1,325)
Which MOMETASONE FUROATE Alternatives Have Lower Device malfunction Risk?
MOMETASONE FUROATE vs MOMETASONE FUROATE\OLOPATADINE
MOMETASONE FUROATE vs MONOMETHYL
MOMETASONE FUROATE vs MONTELUKAST
MOMETASONE FUROATE vs MONTELUKAST\MONTELUKAST
MOMETASONE FUROATE vs MONTMORILLONITE