European Pharmaceutical Review

OCTOBER 17, 2024

This decision was granted a couple of weeks following approval by the US and Drug Administration (FDA). Approximately 40 million people in the US experience Type I allergic reactions due to food, venom or insect stings, 4 and the numbers are similar in Europe. What are the main advantages of EURneffy over similar treatments?

Food and Drug Administration 121

Food and Drug Administration Medicine Consulting Food 121

European Pharmaceutical Review

DECEMBER 18, 2023

Treatment-related side effects included nausea and headache but were generally mild. “As Psilocybin-assisted therapy Psilocybin-assisted therapy combines psilocybin with psychological support from trained therapists.

Food and Drug Administration 116

Food and Drug Administration Patients Side effects Safety 116

Pharmaceutical Technology

JULY 20, 2022

On 6 July, in an effort to accelerate access, the US Food and Drug Administration (FDA) allowed pharmacists to also begin prescribing the drug to eligible individuals with Covid-19. The pharmacist can then review their medical history to make sure there are no concerns of drug-drug interactions with Paxlovid.

Food and Drug Administration 111

Food and Drug Administration Physicians Medical Prescription 111

European Pharmaceutical Review

DECEMBER 27, 2023

Chimeric antigen receptor (CAR) T cells are the first example of a “living drug”. The CAR T cells need to persist in the blood to expand and elicit maximal effect, and there is a correlation between expansion and persistence and response. Furthermore, point-of-care CAR T-cell manufacturing provides clinical benefits.

Manufacturing 104

Manufacturing Food and Drug Administration Patients Pharma 104

Pharma Marketing Network

OCTOBER 3, 2024

Marketers must adhere to regulations set forth by bodies such as the Food and Drug Administration (FDA) in the United States and the European Medicines Agency (EMA) in Europe. Pharmaceutical marketers must provide truthful and non-misleading information about their products, including potential risks and side effects.

Marketing 52

Marketing Pharmaceutical Healthcare Healthcare 52

Healthcare Success

OCTOBER 17, 2024

Lee Aase: As a way of, you know, kind of in keeping with how the Mayo Brothers had done old fashioned analog, social networking in the 1920s, 1930s, visiting lots of countries when they had to go by ship and by air airplane and trained to get there. I'm like, it's controlled drugs. And like you could broadcast without an FCC license.

Healthcare 109

Healthcare Healthcare Patients Insurance 109

European Pharmaceutical Review

NOVEMBER 9, 2023

Following her presentation on age-related disease at BioFuture 2023, Executive Vice President of Drug Development for MyMD Pharmaceuticals ® , Jenna Brager, shares with EPR why the company’s next-generation tumour necrosis factor (TNF)-alpha inhibitor has potential in inflammatory and autoimmune disorders.

Food and Drug Administration 115

Food and Drug Administration Side effects Pharmaceutical Leads 115