BUTENAFINE HYDROCHLORIDE and CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR

Overview

CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR is the #18 most commonly reported adverse reaction for BUTENAFINE HYDROCHLORIDE, manufactured by Bayer Healthcare LLC.. There are 9 FDA adverse event reports linking BUTENAFINE HYDROCHLORIDE to CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR. This represents approximately 1.0% of all 901 adverse event reports for this drug.

Patients taking BUTENAFINE HYDROCHLORIDE who experience circumstance or information capable of leading to 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.

Reporting Frequency

CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR is a less commonly reported adverse event for BUTENAFINE HYDROCHLORIDE, but still significant enough to appear in the safety profile.

Other Side Effects of BUTENAFINE HYDROCHLORIDE

In addition to circumstance or information capable of leading to medication error, the following adverse reactions have been reported for BUTENAFINE HYDROCHLORIDE:

• DRUG INEFFECTIVE — 180 reports
• OFF LABEL USE — 59 reports
• PRODUCT USE ISSUE — 43 reports
• PRODUCT USE IN UNAPPROVED INDICATION — 34 reports
• PRURITUS — 31 reports
• CONDITION AGGRAVATED — 29 reports
• RASH — 21 reports
• DRUG EFFECT DECREASED — 19 reports
• DRUG INEFFECTIVE FOR UNAPPROVED INDICATION — 19 reports
• ERYTHEMA — 19 reports

Other Drugs Associated with CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR

The following drugs have also been linked to circumstance or information capable of leading to medication error in FDA adverse event reports:

Does BUTENAFINE HYDROCHLORIDE cause CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR?

CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR has been reported as an adverse event in 9 FDA reports for BUTENAFINE HYDROCHLORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.

How common is CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR with BUTENAFINE HYDROCHLORIDE?

CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR accounts for approximately 1.0% of all adverse event reports for BUTENAFINE HYDROCHLORIDE, making it a notable side effect.

What should I do if I experience CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR while taking BUTENAFINE HYDROCHLORIDE?

If you experience circumstance or information capable of leading to medication error while taking BUTENAFINE HYDROCHLORIDE, 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.

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