1,094 reports of this reaction
3.1% of all MOMETASONE FUROATE AND FORMOTEROL FUMARATE DIHYDRATE reports
#5 most reported adverse reaction
POOR QUALITY DEVICE USED is the #5 most commonly reported adverse reaction for MOMETASONE FUROATE AND FORMOTEROL FUMARATE DIHYDRATE, manufactured by Organon LLC. There are 1,094 FDA adverse event reports linking MOMETASONE FUROATE AND FORMOTEROL FUMARATE DIHYDRATE to POOR QUALITY DEVICE USED. This represents approximately 3.1% of all 35,067 adverse event reports for this drug.
Patients taking MOMETASONE FUROATE AND FORMOTEROL FUMARATE DIHYDRATE who experience poor quality device used should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
POOR QUALITY DEVICE USED is moderately reported among MOMETASONE FUROATE AND FORMOTEROL FUMARATE DIHYDRATE users, representing a notable but not dominant share of adverse events.
In addition to poor quality device used, the following adverse reactions have been reported for MOMETASONE FUROATE AND FORMOTEROL FUMARATE DIHYDRATE:
The following drugs have also been linked to poor quality device used in FDA adverse event reports:
POOR QUALITY DEVICE USED has been reported as an adverse event in 1,094 FDA reports for MOMETASONE FUROATE AND FORMOTEROL FUMARATE DIHYDRATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
POOR QUALITY DEVICE USED accounts for approximately 3.1% of all adverse event reports for MOMETASONE FUROATE AND FORMOTEROL FUMARATE DIHYDRATE, making it a notable side effect.
If you experience poor quality device used while taking MOMETASONE FUROATE AND FORMOTEROL FUMARATE DIHYDRATE, contact your healthcare provider. They can evaluate whether the symptom is related to your medication and discuss potential adjustments to your treatment plan. Do not stop taking prescribed medication without consulting your doctor.