FDA warns of unapproved potassium phosphates drug product
[8/21/24] FDA remains concerned about the risk of aluminum toxicity associated with use of unapproved potassium phosphates product in pediatric patients, especially when used in parenteral nutrition. FDA is aware that some hospitals continue to buy Hospira’s...FDA warns consumers not to purchase or use EzriCare Artificial Tears
Update [8/25/2023] FDA is reminding the public that these recalled products should not be used, including off-label use in animals. FDA does not have direct knowledge of veterinary use of these products or of animal adverse events that are linked to the products;...FDA alerts health care professionals of risks to patients exposed to x
[11-8-2022] Health care professionals should be cautious of possible xylazine inclusion in fentanyl, heroin, and other illicit drug overdoses, as naloxone may not be able to reverse its effects. FDA is aware of increasing reports of serious side effects from...Bosentan REMS requirements will change June 27, 2022
On April 29, 2022, the U.S. Food and Drug Administration approved a modification to the Bosentan Risk Evaluation and Mitigation Strategy (REMS) program. Beginning June 27, 2022, system changes for health care professionals will go into effect. All stakeholders should...All Drug Purchases Are
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