Does MOMETASONE FUROATE Cause Condition aggravated? 293 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 293 reports of Condition aggravated have been filed in association with MOMETASONE FUROATE (Mometasone Furoate). This represents 2.5% of all adverse event reports for MOMETASONE FUROATE.
293
Reports of Condition aggravated with MOMETASONE FUROATE
2.5%
of all MOMETASONE FUROATE reports
21
Deaths
182
Hospitalizations
How Dangerous Is Condition aggravated From MOMETASONE FUROATE?
Of the 293 reports, 21 (7.2%) resulted in death, 182 (62.1%) required hospitalization, and 25 (8.5%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MOMETASONE FUROATE. However, 293 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which MOMETASONE FUROATE Alternatives Have Lower Condition aggravated Risk?
MOMETASONE FUROATE vs MOMETASONE FUROATE\OLOPATADINE
MOMETASONE FUROATE vs MONOMETHYL
MOMETASONE FUROATE vs MONTELUKAST
MOMETASONE FUROATE vs MONTELUKAST\MONTELUKAST
MOMETASONE FUROATE vs MONTMORILLONITE