US FDA approves AstraZeneca's flu vaccine for self-administration
FluMist is the first vaccine to prevent influenza that does not need to be administered by a healthcare provider, the ...
STAT18m
FDA’s new head of device safety held senior role at company troubled by safety warnings
“Olympus’ continued failure to meet FDA requirements demonstrates a troubling disregard for patient safety,” said Jeffrey ...
FDA Approves Zevra's Miplyffa for Niemann-Pick Disease Type C — Update
Zevra Therapeutics has won Food and Drug Administration approval of Miplyffa for Niemann-Pick disease type C, or NPC, making it the first drug cleared in the U.S. for the rare neurodegenerative ...
FDA Approves Nasal Spray Influenza Vaccine for Self- or Caregiver-Administration
Today, the U.S. Food and Drug Administration approved FluMist for self- or caregiver-administration. FluMist is approved for the prevention of influenza disease caused by influenza virus subtypes A ...
Revised Schedule M compliant: Teams formed to inspect drug units
Indore: The food and drugs administration (FDA) department has identified over 40 pharmaceutical enterprises in Madhya Pradesh that has to undergo com.
Psyence Group Enters into Agreement to Dispose of Stake in PsyLabs
The completion of the Proposed Transaction is subject to the fulfilment, or waiver, of certain conditions, including board approvals, regulatory approvals, a satisfactory due diligence process, and ...
Health.com33m
Multiple Reports Have Found Lead in Cinnamon—Is It Still Safe to Eat?
Recent testing from Consumer Reports and the FDA has found elevated levels of lead in cinnamon products and spice mixes. You ...
REDNVIA eyes US market with repurposed drug for heart valve disorder
Creating a novel drug has always been a risky endeavor for biopharmaceutical companies. Developers and investors face ...
Punchng on MSN37m
NAFDAC warns of substandard antimalaria, antibiotics in circulation
The National Agency for Food and Drug Administration and Control has raised the alarm over the circulation of substandard and ...
Nationwide Snack Recall Update As FDA Sets Highest Risk Level
The snacks now have a Class I risk level, meaning there is a "reasonable probability" they could cause "serious adverse ...
precisionmedicineonline40m
Janssen's Rybrevant, Chemo Regimen Nets FDA Approval in EGFR-Mutated NSCLC
The agency reviewed data from the MARIPOSA-2 trial and approved the regimen for patients with common EGFR mutations who are progressing on EGFR inhibitors.