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Agency will require a Limitation of Use section in the prescribing information of all extended-release ADHD stimulants.
The U.S. Food and Drug Administration is revising the labeling of all extended-release attention-deficit/hyperactivity ...
Ballari (Karnataka) Jun 18 (PTI) Bodies of a woman and her three children were found floating in a pond in a village in Ballari district on Wednesday. Police suspect it to be a case of suicide though ...
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movie review ★★★ ‘Elio:’ Close Encounters of the Nerd Kind Disney/Pixar’s enjoyable space story will appeal more to sci-fi fans than their young kids. Zoe Saldaña stars.
Abstract and Introduction Abstract Purpose. Tenfold dosing medication errors reported to U.S. poison control centers in children younger than six years of age were evaluated. Methods. A ...
This approval expands the approved dosing options for prescribers treating LEMS as well as broadening the indication to include pediatric patients. "We are pleased to receive the approval for both the ...
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Celltrion secures FDA nod for STEQEYMA® pediatric dosing - MSNINCHEON, South Korea, June 16, 2025 /PRNewswire/ -- Celltrion, Inc. today announced that the U.S. Food and Drug Administration (FDA) has approved a new presentation of STEQEYMA® (ustekinumab-stba ...
The FDA previously approved STEQEYMA® 45mg/0.5mL, 90mg/mL in a single-dose prefilled syringe for subcutaneous injection, and 130mg/26mL in a single-dose vial for intravenous infusion in December 2024 ...
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