Does FORMOTEROL\MOMETASONE FUROATE Cause Device issue? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Device issue have been filed in association with FORMOTEROL\MOMETASONE FUROATE. This represents 0.1% of all adverse event reports for FORMOTEROL\MOMETASONE FUROATE.
5
Reports of Device issue with FORMOTEROL\MOMETASONE FUROATE
0.1%
of all FORMOTEROL\MOMETASONE FUROATE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Device issue From FORMOTEROL\MOMETASONE FUROATE?
Of the 5 reports.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FORMOTEROL\MOMETASONE FUROATE. However, 5 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 issue?
ADALIMUMAB (17,630)
SOMATROPIN (5,131)
PEGFILGRASTIM (5,071)
ETANERCEPT (4,143)
INSULIN GLARGINE (3,175)
EXENATIDE (2,862)
LEVONORGESTREL (2,623)
CARBIDOPA\LEVODOPA (2,574)
GOLIMUMAB (1,827)
USTEKINUMAB (1,716)
Which FORMOTEROL\MOMETASONE FUROATE Alternatives Have Lower Device issue 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