1 reports of this reaction
2.3% of all NIGHTTIME COLD AND FLU RELIEF reports
#7 most reported adverse reaction
ASTHMA is the #7 most commonly reported adverse reaction for NIGHTTIME COLD AND FLU RELIEF, manufactured by Advanced Rx LLC. There are 1 FDA adverse event reports linking NIGHTTIME COLD AND FLU RELIEF to ASTHMA. This represents approximately 2.3% of all 43 adverse event reports for this drug.
Patients taking NIGHTTIME COLD AND FLU RELIEF who experience asthma should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
ASTHMA is a less commonly reported adverse event for NIGHTTIME COLD AND FLU RELIEF, but still significant enough to appear in the safety profile.
In addition to asthma, the following adverse reactions have been reported for NIGHTTIME COLD AND FLU RELIEF:
The following drugs have also been linked to asthma in FDA adverse event reports:
ASTHMA has been reported as an adverse event in 1 FDA reports for NIGHTTIME COLD AND FLU RELIEF. This does not prove causation, but indicates an association observed in post-market surveillance data.
ASTHMA accounts for approximately 2.3% of all adverse event reports for NIGHTTIME COLD AND FLU RELIEF, making it a notable side effect.
If you experience asthma while taking NIGHTTIME COLD AND FLU RELIEF, 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.