FDA: Policy Allows for Expanded Use of Certain Remote Patient Monitoring Devices
The policy is intended to remain in effect only for the duration of the COVID-19 public health emergency declared by the Department of Health and Human Services (HHS).
The policy is intended to remain in effect only for the duration of the COVID-19 public health emergency declared by the Department of Health and Human Services (HHS).
For patients suspected of having COVID-19, undergoing REMS-required testing to obtain a medication may put others at risk.
The American College of Allergy, Asthma and Immunology announced a growing shortage of albuterol inhalers in certain areas throughout the US during the COVID-19 pandemic.
Reports show infectee can develop symptoms before infector, indicating presymptomatic transmission.
In patients who were hospitalized with severe coronavirus disease, treatment with lopinavir-ritonavir did not provide a substantial benefit beyond standard care.
The FDA announced that it is working closely with other government agencies and academic centers to investigate the potential use of chloroquine for the treatment of coronavirus disease 2019 (COVID-19).
The FDA has issued a statement regarding the use of nonsteroidal anti-inflammatory drugs (NSAIDS) in patients with coronavirus disease 2019 (COVID-19).
Preparedness includes early detection and limiting exposure of health care workers, hospital employees
This week we talk about a phase 1 trial for a potential COVID-19 vaccine that is underway in Seattle; Concerns over COVID-19 and ACE inhibitor, ARB use; Safety labeling changes for SGLT2 inhibitors; A biosimilar to Herceptin; And new graphic warnings for cigarette packages.
Face mask shortage prompting the CDC to suggest the use of bandannas, if necessary.