12 reports of this reaction
2.1% of all ANTIFUNGAL LIQUID SPRAY reports
#5 most reported adverse reaction
BLOOD POTASSIUM INCREASED is the #5 most commonly reported adverse reaction for ANTIFUNGAL LIQUID SPRAY, manufactured by ARMY & AIR FORCE EXCHANGE SERVICE. There are 12 FDA adverse event reports linking ANTIFUNGAL LIQUID SPRAY to BLOOD POTASSIUM INCREASED. This represents approximately 2.1% of all 575 adverse event reports for this drug.
Patients taking ANTIFUNGAL LIQUID SPRAY who experience blood potassium increased should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
BLOOD POTASSIUM INCREASED is a less commonly reported adverse event for ANTIFUNGAL LIQUID SPRAY, but still significant enough to appear in the safety profile.
In addition to blood potassium increased, the following adverse reactions have been reported for ANTIFUNGAL LIQUID SPRAY:
The following drugs have also been linked to blood potassium increased in FDA adverse event reports:
BLOOD POTASSIUM INCREASED has been reported as an adverse event in 12 FDA reports for ANTIFUNGAL LIQUID SPRAY. This does not prove causation, but indicates an association observed in post-market surveillance data.
BLOOD POTASSIUM INCREASED accounts for approximately 2.1% of all adverse event reports for ANTIFUNGAL LIQUID SPRAY, making it a notable side effect.
If you experience blood potassium increased while taking ANTIFUNGAL LIQUID SPRAY, 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.