1,101 reports of this reaction
1.7% of all ATOMOXETINE HYDROCHLORIDE reports
#11 most reported adverse reaction
PRESCRIBED OVERDOSE is the #11 most commonly reported adverse reaction for ATOMOXETINE HYDROCHLORIDE, manufactured by Eli Lilly and Company. There are 1,101 FDA adverse event reports linking ATOMOXETINE HYDROCHLORIDE to PRESCRIBED OVERDOSE. This represents approximately 1.7% of all 63,960 adverse event reports for this drug.
Patients taking ATOMOXETINE HYDROCHLORIDE who experience prescribed overdose should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
PRESCRIBED OVERDOSE is a less commonly reported adverse event for ATOMOXETINE HYDROCHLORIDE, but still significant enough to appear in the safety profile.
In addition to prescribed overdose, the following adverse reactions have been reported for ATOMOXETINE HYDROCHLORIDE:
The following drugs have also been linked to prescribed overdose in FDA adverse event reports:
PRESCRIBED OVERDOSE has been reported as an adverse event in 1,101 FDA reports for ATOMOXETINE HYDROCHLORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
PRESCRIBED OVERDOSE accounts for approximately 1.7% of all adverse event reports for ATOMOXETINE HYDROCHLORIDE, making it a notable side effect.
If you experience prescribed overdose while taking ATOMOXETINE 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.