Simplivia's Chemfort® Closed System Drug-Transfer Device (CSTD) prevents the escape of hazardous drugs and drug vapors during preparation and administration.
The present invention provides safe pharmaceutical formulations for drugs used in the treatment of drug addiction, namely formulations which render the abusive administration of the drug contained in these formulations not feasible, together with processes for obtaining said formulations....
“Generic drugs are required to have the same active ingredient, strength, dosage form, and route of administration as the brand name product. Generic drug manufacturers must prove their product is the same as (bioequivalent) the brand name product.”– U.S. Food and Drug Administration[1] ...
A safe injection site is a medically supervised facility where individuals may use pre-obtained illicit drugs in a hygienic environment where trained staff are available to intervene in case of an overdose.
The U.S. Food and Drug Administration (FDA) recommends never taking drugs beyond their expiration date as it is risky with many unknown variables. For example, how your drug is stored before and after you receive it, chemical make-up, and original manufacturing date can all affect potency ...
U.S. Food and Drug Administration (FDA). Tablet Splitting. Updated 8/23/2013. Accessed August 9, 2024. https://www.fda.gov/drugs/buying-using-medicine-safely/tablet-splitting Elliott I, Mayxay M, Yeuichaixong S, et al. The practice and clinical implications of tablet splitting in intern...
Medication administration phase: Products could be removed for a discharged patient, medications might be documented as administered but not provided to patients, or substitute drugs might be administered in place of the product. Waste and removal phase:Controlled-substance waste might be removed from ...
1 For example, potassium chloride injection has a narrow safety index in veterinary patients and can interact with many other drugs when used in combination. Awareness of this drug’s maximum concentration and maximum rate of administration is important for patient safety.5 Awareness & Prevention...
The U.S. Food and Drug Administration dropped its “in-person” dispensing requirement for the first drug in medical abortion, mifepristone, in 2021, although the decision is part of what is now being challenged in the Supreme Court. The study found that 97.7% of a...
Anaphylactic reaction owing to ondansetron administration in a child with neuroblastoma and safe use of granisetron: a case report. A 1-year-old girl with stage-IV neuroblastoma developed ondansetron hydrochloride anaphylaxis. Safe use of granisetron as an antiemetic after skin prick, o... HA Demir...