1 reports of this reaction
3.8% of all CAMPHOR (SYNTHETIC) reports
#15 most reported adverse reaction
MEDICATION ERROR is the #15 most commonly reported adverse reaction for CAMPHOR (SYNTHETIC), manufactured by Kaz USA, Inc. There are 1 FDA adverse event reports linking CAMPHOR (SYNTHETIC) to MEDICATION ERROR. This represents approximately 3.8% of all 26 adverse event reports for this drug.
Patients taking CAMPHOR (SYNTHETIC) who experience medication error should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
MEDICATION ERROR is moderately reported among CAMPHOR (SYNTHETIC) users, representing a notable but not dominant share of adverse events.
In addition to medication error, the following adverse reactions have been reported for CAMPHOR (SYNTHETIC):
The following drugs have also been linked to medication error in FDA adverse event reports:
MEDICATION ERROR has been reported as an adverse event in 1 FDA reports for CAMPHOR (SYNTHETIC). This does not prove causation, but indicates an association observed in post-market surveillance data.
MEDICATION ERROR accounts for approximately 3.8% of all adverse event reports for CAMPHOR (SYNTHETIC), making it a notable side effect.
If you experience medication error while taking CAMPHOR (SYNTHETIC), 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.