PANTHENOL and ANAEMIA

Overview

ANAEMIA is the #8 most commonly reported adverse reaction for PANTHENOL, manufactured by LAON COMMERCE co ltd. There are 28 FDA adverse event reports linking PANTHENOL to ANAEMIA. This represents approximately 1.8% of all 1,581 adverse event reports for this drug.

Patients taking PANTHENOL who experience anaemia 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

ANAEMIA is a less commonly reported adverse event for PANTHENOL, but still significant enough to appear in the safety profile.

Other Side Effects of PANTHENOL

In addition to anaemia, the following adverse reactions have been reported for PANTHENOL:

• NAUSEA — 42 reports
• GENERAL PHYSICAL HEALTH DETERIORATION — 37 reports
• CONDITION AGGRAVATED — 31 reports
• DYSPNOEA — 31 reports
• VOMITING — 31 reports
• ABDOMINAL PAIN — 30 reports
• PYREXIA — 30 reports
• DRY MOUTH — 27 reports
• ASTHENIA — 23 reports
• BLOOD CHOLESTEROL INCREASED — 23 reports

Other Drugs Associated with ANAEMIA

The following drugs have also been linked to anaemia in FDA adverse event reports:

Does PANTHENOL cause ANAEMIA?

ANAEMIA has been reported as an adverse event in 28 FDA reports for PANTHENOL. This does not prove causation, but indicates an association observed in post-market surveillance data.

How common is ANAEMIA with PANTHENOL?

ANAEMIA accounts for approximately 1.8% of all adverse event reports for PANTHENOL, making it a notable side effect.

What should I do if I experience ANAEMIA while taking PANTHENOL?

If you experience anaemia while taking PANTHENOL, 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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