1 reports of this reaction
9.1% of all HYOSCYAMUS NIGER reports
#10 most reported adverse reaction
MYDRIASIS is the #10 most commonly reported adverse reaction for HYOSCYAMUS NIGER, manufactured by Amneal Pharmaceuticals LLC. There are 1 FDA adverse event reports linking HYOSCYAMUS NIGER to MYDRIASIS. This represents approximately 9.1% of all 11 adverse event reports for this drug.
Patients taking HYOSCYAMUS NIGER who experience mydriasis should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
MYDRIASIS is moderately reported among HYOSCYAMUS NIGER users, representing a notable but not dominant share of adverse events.
In addition to mydriasis, the following adverse reactions have been reported for HYOSCYAMUS NIGER:
The following drugs have also been linked to mydriasis in FDA adverse event reports:
MYDRIASIS has been reported as an adverse event in 1 FDA reports for HYOSCYAMUS NIGER. This does not prove causation, but indicates an association observed in post-market surveillance data.
MYDRIASIS accounts for approximately 9.1% of all adverse event reports for HYOSCYAMUS NIGER, making it a notable side effect.
If you experience mydriasis while taking HYOSCYAMUS NIGER, 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.