282 reports of this reaction
2.3% of all BECLOMETHASONE DIPROPIONATE reports
#9 most reported adverse reaction
MALAISE is the #9 most commonly reported adverse reaction for BECLOMETHASONE DIPROPIONATE. There are 282 FDA adverse event reports linking BECLOMETHASONE DIPROPIONATE to MALAISE. This represents approximately 2.3% of all 12,391 adverse event reports for this drug.
Patients taking BECLOMETHASONE DIPROPIONATE who experience malaise should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
MALAISE is a less commonly reported adverse event for BECLOMETHASONE DIPROPIONATE, but still significant enough to appear in the safety profile.
In addition to malaise, the following adverse reactions have been reported for BECLOMETHASONE DIPROPIONATE:
The following drugs have also been linked to malaise in FDA adverse event reports:
MALAISE has been reported as an adverse event in 282 FDA reports for BECLOMETHASONE DIPROPIONATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
MALAISE accounts for approximately 2.3% of all adverse event reports for BECLOMETHASONE DIPROPIONATE, making it a notable side effect.
If you experience malaise while taking BECLOMETHASONE DIPROPIONATE, 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.