METHYLPHENIDATE HYDROCHLORIDE and FEELING ABNORMAL
1,751 reports of this reaction
1.7% of all METHYLPHENIDATE HYDROCHLORIDE reports
#11 most reported adverse reaction
Overview
FEELING ABNORMAL is the #11 most commonly reported adverse reaction for METHYLPHENIDATE HYDROCHLORIDE, manufactured by Sandoz Inc. There are 1,751 FDA adverse event reports linking METHYLPHENIDATE HYDROCHLORIDE to FEELING ABNORMAL. This represents approximately 1.7% of all 101,957 adverse event reports for this drug.
Patients taking METHYLPHENIDATE HYDROCHLORIDE who experience feeling abnormal should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
Reporting Frequency
FEELING ABNORMAL1,751 of 101,957 reports
FEELING ABNORMAL is a less commonly reported adverse event for METHYLPHENIDATE HYDROCHLORIDE, but still significant enough to appear in the safety profile.
Other Side Effects of METHYLPHENIDATE HYDROCHLORIDE
In addition to feeling abnormal, the following adverse reactions have been reported for METHYLPHENIDATE HYDROCHLORIDE:
Does METHYLPHENIDATE HYDROCHLORIDE cause FEELING ABNORMAL?
FEELING ABNORMAL has been reported as an adverse event in 1,751 FDA reports for METHYLPHENIDATE HYDROCHLORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
How common is FEELING ABNORMAL with METHYLPHENIDATE HYDROCHLORIDE?
FEELING ABNORMAL accounts for approximately 1.7% of all adverse event reports for METHYLPHENIDATE HYDROCHLORIDE, making it a notable side effect.
What should I do if I experience FEELING ABNORMAL while taking METHYLPHENIDATE HYDROCHLORIDE?
If you experience feeling abnormal while taking METHYLPHENIDATE HYDROCHLORIDE, 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.
Disclaimer: This analysis is based on FDA adverse event reports and is for informational purposes only. Reports do not prove causation. Always consult your healthcare provider.