5 reports of this reaction
5.8% of all PULSATILLA VULGARIS reports
#1 most reported adverse reaction
HYPOTHERMIA is the #1 most commonly reported adverse reaction for PULSATILLA VULGARIS. There are 5 FDA adverse event reports linking PULSATILLA VULGARIS to HYPOTHERMIA. This represents approximately 5.8% of all 86 adverse event reports for this drug.
Patients taking PULSATILLA VULGARIS who experience hypothermia should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
HYPOTHERMIA is moderately reported among PULSATILLA VULGARIS users, representing a notable but not dominant share of adverse events.
In addition to hypothermia, the following adverse reactions have been reported for PULSATILLA VULGARIS:
HYPOTHERMIA has been reported as an adverse event in 5 FDA reports for PULSATILLA VULGARIS. This does not prove causation, but indicates an association observed in post-market surveillance data.
HYPOTHERMIA accounts for approximately 5.8% of all adverse event reports for PULSATILLA VULGARIS, making it one of the most commonly reported side effect.
If you experience hypothermia while taking PULSATILLA VULGARIS, 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.