15 reports of this reaction
1.1% of all HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK reports
#15 most reported adverse reaction
GENERAL PHYSICAL HEALTH DETERIORATION is the #15 most commonly reported adverse reaction for HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK, manufactured by Boiron. There are 15 FDA adverse event reports linking HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK to GENERAL PHYSICAL HEALTH DETERIORATION. This represents approximately 1.1% of all 1,361 adverse event reports for this drug.
Patients taking HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK who experience general physical health deterioration should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
GENERAL PHYSICAL HEALTH DETERIORATION is a less commonly reported adverse event for HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK, but still significant enough to appear in the safety profile.
In addition to general physical health deterioration, the following adverse reactions have been reported for HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK:
The following drugs have also been linked to general physical health deterioration in FDA adverse event reports:
GENERAL PHYSICAL HEALTH DETERIORATION has been reported as an adverse event in 15 FDA reports for HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK. This does not prove causation, but indicates an association observed in post-market surveillance data.
GENERAL PHYSICAL HEALTH DETERIORATION accounts for approximately 1.1% of all adverse event reports for HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK, making it a notable side effect.
If you experience general physical health deterioration while taking HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK, 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.