2 reports of this reaction
4.7% of all NIGHTTIME COLD AND FLU RELIEF reports
#1 most reported adverse reaction
MIOSIS is the #1 most commonly reported adverse reaction for NIGHTTIME COLD AND FLU RELIEF, manufactured by Advanced Rx LLC. There are 2 FDA adverse event reports linking NIGHTTIME COLD AND FLU RELIEF to MIOSIS. This represents approximately 4.7% of all 43 adverse event reports for this drug.
Patients taking NIGHTTIME COLD AND FLU RELIEF who experience miosis should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
MIOSIS is moderately reported among NIGHTTIME COLD AND FLU RELIEF users, representing a notable but not dominant share of adverse events.
In addition to miosis, the following adverse reactions have been reported for NIGHTTIME COLD AND FLU RELIEF:
MIOSIS has been reported as an adverse event in 2 FDA reports for NIGHTTIME COLD AND FLU RELIEF. This does not prove causation, but indicates an association observed in post-market surveillance data.
MIOSIS accounts for approximately 4.7% of all adverse event reports for NIGHTTIME COLD AND FLU RELIEF, making it one of the most commonly reported side effect.
If you experience miosis 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.