1 reports of this reaction
3.8% of all CAMPHOR (SYNTHETIC) reports
#20 most reported adverse reaction
PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE is the #20 most commonly reported adverse reaction for CAMPHOR (SYNTHETIC), manufactured by Kaz USA, Inc. There are 1 FDA adverse event reports linking CAMPHOR (SYNTHETIC) to PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE. This represents approximately 3.8% of all 26 adverse event reports for this drug.
Patients taking CAMPHOR (SYNTHETIC) who experience product administered to patient of inappropriate age should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE is moderately reported among CAMPHOR (SYNTHETIC) users, representing a notable but not dominant share of adverse events.
In addition to product administered to patient of inappropriate age, the following adverse reactions have been reported for CAMPHOR (SYNTHETIC):
The following drugs have also been linked to product administered to patient of inappropriate age in FDA adverse event reports:
PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE 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.
PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE accounts for approximately 3.8% of all adverse event reports for CAMPHOR (SYNTHETIC), making it a notable side effect.
If you experience product administered to patient of inappropriate age 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.