NIACINAMIDE and OFF LABEL USE

Overview

OFF LABEL USE is the #1 most commonly reported adverse reaction for NIACINAMIDE, manufactured by Garam Of Nature. There are 108 FDA adverse event reports linking NIACINAMIDE to OFF LABEL USE. This represents approximately 5.2% of all 2,059 adverse event reports for this drug.

Patients taking NIACINAMIDE who experience off label use 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

OFF LABEL USE is moderately reported among NIACINAMIDE users, representing a notable but not dominant share of adverse events.

Other Side Effects of NIACINAMIDE

In addition to off label use, the following adverse reactions have been reported for NIACINAMIDE:

• FATIGUE — 78 reports
• DRUG INEFFECTIVE — 67 reports
• DIARRHOEA — 54 reports
• SOMNOLENCE — 50 reports
• GASTROOESOPHAGEAL REFLUX DISEASE — 49 reports
• HEADACHE — 48 reports
• NAUSEA — 48 reports
• PNEUMONIA ASPIRATION — 41 reports
• COMA — 38 reports
• ASTHENIA — 37 reports

Other Drugs Associated with OFF LABEL USE

The following drugs have also been linked to off label use in FDA adverse event reports:

Does NIACINAMIDE cause OFF LABEL USE?

OFF LABEL USE has been reported as an adverse event in 108 FDA reports for NIACINAMIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.

How common is OFF LABEL USE with NIACINAMIDE?

OFF LABEL USE accounts for approximately 5.2% of all adverse event reports for NIACINAMIDE, making it one of the most commonly reported side effect.

What should I do if I experience OFF LABEL USE while taking NIACINAMIDE?

If you experience off label use while taking NIACINAMIDE, 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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