FINASTERIDE and ADVERSE EVENT

Overview

ADVERSE EVENT is the #19 most commonly reported adverse reaction for FINASTERIDE, manufactured by Organon LLC. There are 1,535 FDA adverse event reports linking FINASTERIDE to ADVERSE EVENT. This represents approximately 1.5% of all 103,583 adverse event reports for this drug.

Patients taking FINASTERIDE who experience adverse event 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

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

Other Side Effects of FINASTERIDE

In addition to adverse event, the following adverse reactions have been reported for FINASTERIDE:

• FATIGUE — 3,948 reports
• ERECTILE DYSFUNCTION — 3,933 reports
• DEPRESSION — 3,499 reports
• ANXIETY — 2,966 reports
• DRUG INEFFECTIVE — 2,534 reports
• DIZZINESS — 2,377 reports
• SEXUAL DYSFUNCTION — 2,322 reports
• DIARRHOEA — 2,265 reports
• DEATH — 2,169 reports
• ASTHENIA — 2,106 reports

Other Drugs Associated with ADVERSE EVENT

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

Does FINASTERIDE cause ADVERSE EVENT?

ADVERSE EVENT has been reported as an adverse event in 1,535 FDA reports for FINASTERIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.

How common is ADVERSE EVENT with FINASTERIDE?

ADVERSE EVENT accounts for approximately 1.5% of all adverse event reports for FINASTERIDE, making it a notable side effect.

What should I do if I experience ADVERSE EVENT while taking FINASTERIDE?

If you experience adverse event while taking FINASTERIDE, 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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