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GoodRx released a list of 19 of the most influential drugs and vaccines approved by the FDA in 2024 to treat a variety of conditions. These medications are “slated to make a big clinical impact."
The drug brought in annual sales of $1.66 billion as of April 2024, according to Teva. Teva's generic launch comes days after the U.S. Food and Drug Administration tentatively approved London ...
2024 could bring more effective ways to treat Alzheimer’s, schizophrenia, and hemophilia. ... 2023 was a strong year for innovative new drugs, with new medications for Alzheimer’s disease, ...
The American Society of Health-System Pharmacists (ASHP) reported that 323 "active medication shortages" were reported in January–March 2024. As a result of drug scarcity, many healthcare systems were forced to either ration out essential drugs, triage patients based on the severity of their condition and their need for the drug, or both.
In most cases, generic products become available after the patent protections afforded to the drug's original developer expire. Once generic drugs enter the market, competition often leads to substantially lower prices for both the original brand-name product and its generic equivalents. In most countries, patents give 20 years of protection.
Pharmacists are significantly involved in advising patients on the use of medications, particularly generic drugs, which have become prevalent as a cost-saving measure in the healthcare system. While pharmacists can suggest the substitution of prescribed medications with generics, the final decision usually remains with the prescribing physician.
The initial list includes common prescriptions such as penicillin, metformin, lithium and albuterol asthma inhalers, as well as drugs for high cholesterol, high blood pressure and other chronic ...
Authorized generics are prescription drugs produced by brand pharmaceutical companies and marketed under a private label, at generic prices. Authorized generics compete with generic products in that they are identical to their brand counterpart in both active and inactive ingredients; [1] whereas according to the U.S. Food and Drug Administration's Office of Generic Drugs, generic drugs are ...