CALENDULA OFFICINALIS and BURNS FIRST DEGREE

1 reports of this reaction

1.8% of all CALENDULA OFFICINALIS reports

#11 most reported adverse reaction

Overview

BURNS FIRST DEGREE is the #11 most commonly reported adverse reaction for CALENDULA OFFICINALIS, manufactured by Seroyal USA. There are 1 FDA adverse event reports linking CALENDULA OFFICINALIS to BURNS FIRST DEGREE. This represents approximately 1.8% of all 56 adverse event reports for this drug.

Patients taking CALENDULA OFFICINALIS who experience burns first degree 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

BURNS FIRST DEGREE1 of 56 reports

BURNS FIRST DEGREE is a less commonly reported adverse event for CALENDULA OFFICINALIS, but still significant enough to appear in the safety profile.

Other Side Effects of CALENDULA OFFICINALIS

In addition to burns first degree, the following adverse reactions have been reported for CALENDULA OFFICINALIS:

Frequently Asked Questions

Does CALENDULA OFFICINALIS cause BURNS FIRST DEGREE?

BURNS FIRST DEGREE has been reported as an adverse event in 1 FDA reports for CALENDULA OFFICINALIS. This does not prove causation, but indicates an association observed in post-market surveillance data.

How common is BURNS FIRST DEGREE with CALENDULA OFFICINALIS?

BURNS FIRST DEGREE accounts for approximately 1.8% of all adverse event reports for CALENDULA OFFICINALIS, making it a notable side effect.

What should I do if I experience BURNS FIRST DEGREE while taking CALENDULA OFFICINALIS?

If you experience burns first degree while taking CALENDULA OFFICINALIS, 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.

Related Pages

CALENDULA OFFICINALIS Full ProfileAll Drugs Causing BURNS FIRST DEGREESeroyal USA Drugs
Disclaimer: This analysis is based on FDA adverse event reports and is for informational purposes only. Reports do not prove causation. Always consult your healthcare provider.