Does MOMETASONE FUROATE Cause Poor quality device used? 2,159 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 2,159 reports of Poor quality device used have been filed in association with MOMETASONE FUROATE (Mometasone Furoate). This represents 18.6% of all adverse event reports for MOMETASONE FUROATE.
2,159
Reports of Poor quality device used with MOMETASONE FUROATE
18.6%
of all MOMETASONE FUROATE reports
0
Deaths
29
Hospitalizations
How Dangerous Is Poor quality device used From MOMETASONE FUROATE?
Of the 2,159 reports, 29 (1.3%) required hospitalization, and 2 (0.1%) were considered life-threatening.
Is Poor quality device used Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MOMETASONE FUROATE. However, 2,159 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)
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 Poor quality device used?
SOMATROPIN (3,162)
ALBUTEROL (1,251)
FORMOTEROL\MOMETASONE FUROATE (1,091)
MEDROXYPROGESTERONE (80)
ETHINYL ESTRADIOL\ETONOGESTREL (77)
FOLLITROPIN (58)
ETONOGESTREL (55)
ETANERCEPT (46)
ESTRADIOL (41)
PEGFILGRASTIM (38)
Which MOMETASONE FUROATE Alternatives Have Lower Poor quality device used Risk?
MOMETASONE FUROATE vs MOMETASONE FUROATE\OLOPATADINE
MOMETASONE FUROATE vs MONOMETHYL
MOMETASONE FUROATE vs MONTELUKAST
MOMETASONE FUROATE vs MONTELUKAST\MONTELUKAST
MOMETASONE FUROATE vs MONTMORILLONITE