What Led to the Recall of Zantac?

The US Food and Drug Administration (FDA) is responsible for protecting public health by enacting measures that ensure the efficacy, safety, and security of human

The Risks of NDMA

N-nitrosodimethylamine, or NDMA, is a naturally-occurring chemical that can become carcinogenic if repeatedly ingested in large amounts. In recent years, the chemical has been discovered

Who Qualifies For A Zantac Lawsuit?

Zantac and other ranitidine-based drugs were recalled by the US Food and Drug Administration (FDA) on April 1st, 2020 because of their connection to the