41 reports of this reaction
2.0% of all NIACINAMIDE reports
#9 most reported adverse reaction
PNEUMONIA ASPIRATION is the #9 most commonly reported adverse reaction for NIACINAMIDE, manufactured by Garam Of Nature. There are 41 FDA adverse event reports linking NIACINAMIDE to PNEUMONIA ASPIRATION. This represents approximately 2.0% of all 2,059 adverse event reports for this drug.
Patients taking NIACINAMIDE who experience pneumonia aspiration should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
PNEUMONIA ASPIRATION is a less commonly reported adverse event for NIACINAMIDE, but still significant enough to appear in the safety profile.
In addition to pneumonia aspiration, the following adverse reactions have been reported for NIACINAMIDE:
The following drugs have also been linked to pneumonia aspiration in FDA adverse event reports:
PNEUMONIA ASPIRATION has been reported as an adverse event in 41 FDA reports for NIACINAMIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
PNEUMONIA ASPIRATION accounts for approximately 2.0% of all adverse event reports for NIACINAMIDE, making it a notable side effect.
If you experience pneumonia aspiration while taking NIACINAMIDE, 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.