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16/06/25 08:01

States Are Making It Easier to Get Ivermectin

In recent years, ivermectin has become a widely discussed drug, particularly in the context of the COVID-19 pandemic. Traditionally used as an antiparasitic medication for both humans and animals, ivermectin gained attention for its potential off-label use in treating COVID-19 symptoms. Despite ongoing debates about its efficacy and safety for viral infections, several U.S. states have moved to make it easier for residents to access this medication. This article explores the legislative and regulatory changes unfolding across states, the implications for public health, and the broader context surrounding ivermectin’s accessibility.

Background: Understanding Ivermectin’s Medical Use

Ivermectin is an FDA-approved medicine primarily used to treat parasitic infections such as river blindness, scabies, and certain types of worms. The drug’s antiparasitic properties have made it a staple in tropical medicine and veterinary care. However, the global COVID-19 crisis sparked interest in whether ivermectin could also provide antiviral benefits.

Initial laboratory studies suggested that ivermectin might inhibit the replication of SARS-CoV-2, the virus responsible for COVID-19. Despite some early enthusiasm, large-scale clinical trials and health authorities, including the FDA and WHO, have generally advised against using ivermectin for COVID-19 outside controlled clinical trials due to insufficient evidence supporting its effectiveness and concerns over dosage and safety.

Why Are States Making It Easier to Get Ivermectin?

In response to public demand and a desire to increase treatment options during the ongoing pandemic, some states have implemented policies to ease access to ivermectin. These changes include:

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