Does FORMOTEROL\MOMETASONE FUROATE Cause Device malfunction? 655 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 655 reports of Device malfunction have been filed in association with FORMOTEROL\MOMETASONE FUROATE. This represents 8.0% of all adverse event reports for FORMOTEROL\MOMETASONE FUROATE.
655
Reports of Device malfunction with FORMOTEROL\MOMETASONE FUROATE
8.0%
of all FORMOTEROL\MOMETASONE FUROATE reports
0
Deaths
20
Hospitalizations
How Dangerous Is Device malfunction From FORMOTEROL\MOMETASONE FUROATE?
Of the 655 reports, 20 (3.1%) required hospitalization, and 1 (0.2%) 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 FORMOTEROL\MOMETASONE FUROATE. However, 655 reports have been filed with the FAERS database.
What Other Side Effects Does FORMOTEROL\MOMETASONE FUROATE Cause?
Dyspnoea (2,560)
Asthma (2,482)
Product quality issue (2,458)
No adverse event (2,315)
Wheezing (1,912)
Drug dose omission (1,474)
Therapeutic product effect incomplete (1,394)
Cough (1,188)
Loss of personal independence in daily activities (1,148)
Poor quality device used (1,091)
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)
MOMETASONE FUROATE (1,332)
Which FORMOTEROL\MOMETASONE FUROATE Alternatives Have Lower Device malfunction Risk?
FORMOTEROL\MOMETASONE FUROATE vs FORTEO
FORMOTEROL\MOMETASONE FUROATE vs FOSAMAX
FORMOTEROL\MOMETASONE FUROATE vs FOSAMPRENAVIR
FORMOTEROL\MOMETASONE FUROATE vs FOSAPREPITANT
FORMOTEROL\MOMETASONE FUROATE vs FOSAPREPITANT DIMEGLUMINE