HealthDay News — Girls with mental illness and neurodevelopmental conditions have lower uptake of human papillomavirus (HPV) vaccination, according to a study published in the September issue of The ...

MM-II is a proprietary suspension of large empty liposomes composed of dipalmitoylphosphatidylcholine and dimyristoylphosphatidylcholine.

Vaccination effectiveness did not differ with inverse probability of vaccination weighting or for those aged 60 to 74 years and 75 years and older ...

The Food and Drug Administration (FDA) has granted full approval to Filspari ® (sparsentan) to slow kidney function decline in adults with primary immunoglobulin A (IgA) nephropathy who are at risk ...

Three point six percent did not get prescription medications due to cost; 3.4% did not take medication as prescribed due to cost.

The product can be administered subcutaneously and intravenously, though each route of administration has a different final concentration.

The Food and Drug Administration (FDA) has cleared DaylightRx, a prescription digital therapeutic for the treatment of generalized anxiety disorder (GAD).

The PDUFA date refers to the deadline set by the US Food and Drug Administration for reviewing drug applications.

Humanized mAb directed against pituitary adenylate cyclase-activating polypeptide ligand reduces migraines over 4 weeks ...

HealthDay News — First-generation antihistamines are associated with a higher seizure risk in young children, according to a study published online August 28 in JAMA Network Open.

HealthDay News — Inhaler devices are a substantial source of greenhouse gas emissions in the US, according to a research letter published online August 29 in the Journal of the American Medical ...

The Food and Drug Administration (FDA) has authorized the emergency use of the Novavax COVID-19 Vaccine, Adjuvanted (2024-2025 Formula). The 2023-2024 formulation of the vaccine is no longer ...