13 reports of this reaction
1.4% of all NEOSTIGMINE METHYLSULFATE reports
#18 most reported adverse reaction
DEMENTIA is the #18 most commonly reported adverse reaction for NEOSTIGMINE METHYLSULFATE, manufactured by Exela Pharma Sciences, LLC. There are 13 FDA adverse event reports linking NEOSTIGMINE METHYLSULFATE to DEMENTIA. This represents approximately 1.4% of all 959 adverse event reports for this drug.
NEOSTIGMINE METHYLSULFATE has an overall safety score of 85 out of 100. Patients taking NEOSTIGMINE METHYLSULFATE who experience dementia should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DEMENTIA is a less commonly reported adverse event for NEOSTIGMINE METHYLSULFATE, but still significant enough to appear in the safety profile.
In addition to dementia, the following adverse reactions have been reported for NEOSTIGMINE METHYLSULFATE:
The following drugs have also been linked to dementia in FDA adverse event reports:
DEMENTIA has been reported as an adverse event in 13 FDA reports for NEOSTIGMINE METHYLSULFATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
DEMENTIA accounts for approximately 1.4% of all adverse event reports for NEOSTIGMINE METHYLSULFATE, making it a notable side effect.
If you experience dementia while taking NEOSTIGMINE METHYLSULFATE, 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.