Remove 2024 Remove Adverse Reactions Remove Vaccines
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Moderna receives U.S. FDA approval for RSV vaccine mRESVIA(R)

Express Pharma

mRESVIA is Moderna’s second approved product and reportedly the only RSV vaccine available in single-dose pre-filled syringes Moderna, announced that the U.S. This approval is also the first time an mRNA vaccine has been approved for a disease other than COVID-19. The primary analysis with 3.7 per cent (95.88 per cent CI 66.0

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Novavax’s updated Covid-19 vaccine receives FDA emergency use authorisation

Pharmaceutical Business Review

The Novavax COVID-19 Vaccine, Adjuvanted (2024-2025 Formula) [NVX-CoV2705] is now authorised for active immunisation against Covid-19. Following the EUA, the vaccine is also recommended by the US Centers for Disease Control and Prevention (CDC). Our updated vaccine targets JN.1, 1.” “Our updated vaccine targets JN.1,

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First chikungunya vaccine approved

European Pharmaceutical Review

The US Food and Drug Administration (FDA) has approved Valneva SE’s IXCHIQ ® , the first chikungunya vaccine to be authorised in the world. The single-dose, live-attenuated vaccine is indicated for preventing chikungunya virus disease in individuals over 18 years old who are at increased risk of contracting the virus.

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Every Claim You Make, Every Step You Take…CVM Will Be Watching You

FDA Law Blog: Biosimilars

Elanco is the manufacturer of recently approved Zenrelia (ilunocitinib tablets) (September 2024), which is indicated for control of pruritus associated with allergic dermatitis and control of atopic dermatitis in dogs at least 12 months of age. Further, information presented on the adverse reaction data was inconsistent with the PI.

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Amber Specialty Pharmacy Selected To Dispense NEMLUVIO® (nemolizumab-ilto) by Galderma for Prurigo Nodularis

Amber

12, 2024) – Amber Specialty Pharmacy, a leader in the specialty pharmacy industry, is excited to announce the availability of Galderma’s latest medication, NEMLUVIO® (nemolizumab-ilto), for the treatment of Prurigo Nodularis in adults. Avoid use of live vaccines during treatment with NEMLUVIO. Omaha, Neb.

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Pfizer’s ABRYSVO gains EU approval for RSV prevention in adults 18-59

Express Pharma

Pfizer announced that the European Commission (EC) has amended the marketing authorisation for ABRYSVO, the companys bivalent respiratory syncytial virus (RSV) prefusion F (RSVpreF) vaccine, to include the prevention of lower respiratory tract disease (LRTD) caused by RSV in individuals aged 18 to 59.