
Zantac Recalled Because of NDMA
In a move that was unsurprising, the FDA announced this week that they requesting all Zantac or Ranitinde products be removed from the pharmacies, shelves, stores, and market. The decision has been expected for months.
What an Exciting Day for the Prevention of HIV
As of Monday July 16th – the Food and Drug Administration – approved the Truvada as a prescription medication to prevent high risk patients from being exposed to HIV.