30 reports of this reaction
1.9% of all SELENIUM SULFIDE reports
#10 most reported adverse reaction
PRODUCT ODOUR ABNORMAL is the #10 most commonly reported adverse reaction for SELENIUM SULFIDE, manufactured by Chattem, Inc.. There are 30 FDA adverse event reports linking SELENIUM SULFIDE to PRODUCT ODOUR ABNORMAL. This represents approximately 1.9% of all 1,547 adverse event reports for this drug.
Patients taking SELENIUM SULFIDE who experience product odour 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.
PRODUCT ODOUR ABNORMAL is a less commonly reported adverse event for SELENIUM SULFIDE, but still significant enough to appear in the safety profile.
In addition to product odour abnormal, the following adverse reactions have been reported for SELENIUM SULFIDE:
The following drugs have also been linked to product odour abnormal in FDA adverse event reports:
PRODUCT ODOUR ABNORMAL has been reported as an adverse event in 30 FDA reports for SELENIUM SULFIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
PRODUCT ODOUR ABNORMAL accounts for approximately 1.9% of all adverse event reports for SELENIUM SULFIDE, making it a notable side effect.
If you experience product odour abnormal while taking SELENIUM SULFIDE, 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.