Tag: Liver enzymes

In controlled clinical trials, finasteride has been associated with only a low rate of transient serum aminotransferase elevations, a rate that was often no higher than with placebo. However, questions about long-term use and liver health remain, prompting a closer look at whether is finasteride bad for your liver, particularly for those with pre-existing conditions.

Finasteride was first approved in 1992 and is used to treat both benign prostatic hyperplasia and male pattern hair loss [1.8.3]. A common concern for users is its safety profile: **is finasteride hard on your liver?** This article examines the evidence.

While minoxidil is primarily known for stimulating hair growth, its metabolism in the liver is a crucial step in how the body processes the medication, naturally prompting the question: **Does minoxidil increase liver enzymes?** Medical literature indicates that while uncommon serum aminotransferase elevations have been reported, minoxidil is not convincingly linked to clinically apparent acute liver injury.

Recent case reports have documented severe drug-induced liver injury (DILI) from self-administration of fenbendazole in humans [1.2.1, 1.2.2]. This raises the critical question: is fenbendazole hard on your liver, and what are the actual risks associated with its use?

Many practitioners recommend cycling berberine usage, with some suggesting a break of two to four weeks after an eight-week cycle. Knowing how long of a break should you take from berberine is crucial for maintaining its efficacy, minimizing potential side effects like liver enzyme fluctuations, and preventing disruptions to the gut microbiome.

While millions of people have used alendronate since its approval, serious liver injury is an extremely rare adverse effect. The bisphosphonate medication, most commonly prescribed for osteoporosis, is not significantly metabolized by the liver, which contributes to its generally safe profile concerning hepatic function.

According to the National Library of Medicine, drug-induced liver injury (DILI) is among the most common reasons for liver enzyme elevation. This guide explores **what medications cause high ALT levels** by outlining common culprits, discussing their mechanisms, and explaining the clinical management of medication-related hepatotoxicity.

An estimated 80% to 90% of adults consume some form of caffeine every day, but how it affects you is largely dictated by a single, powerful liver enzyme. This crucial enzyme, known as CYP1A2, dictates your body's ability to process and eliminate caffeine, explaining why some people are unfazed by an espresso while others get the jitters from a single cup.