Patients may report side effects to the FDA at 1-800-FDA-1088. Please click here for the full Prescribing Information, including Patient Information, for JOURNAVX. About Vertex ...
Feb. 5. 2025 – The FDA has approved a new pill to treat adults with a type of blood cancer called mantle cell lymphoma (MCL). This treatment is for people who are newly diagnosed or haven't h ...
WEDNESDAY, Feb. 5, 2025 (HealthDay News) -- The U.S. Food and Drug Administration has approved Symbravo (meloxicam and rizatriptan) for the acute treatment of migraine with or without aura in adults.
The people didn’t elect Elon Musk. The world’s richest man’s approval rating is at its lowest level and a majority of voters say they don’t favor his outsized role in President Donald ...
The FDA is reviewing the application for bentracimab for use as a ticagrelor reversal agent in patients with uncontrolled bleeding or in those who require urgent surgery or invasive procedure.
The US Food and Drug Administration (FDA) has approved Supernus Pharmaceuticals’ Onapgo (apomorphine hydrochloride) injection to treat motor fluctuations in adults with advanced Parkinson’s disease ...
The Nuance Audio smart glasses designed to help those with hearing loss have gained FDA approval, meaning they can be explicitly sold OTC in the US for that purpose. The EssilorLuxottica brand’s ...
The Federal Executive Council (FEC) yesterday approved the issuance of a N758 billion bond to clear pension arrears for retirees. The approval was granted during the Federal Executive Council (FEC ...
Languages: English That has some policy experts confused about the FDA's ability to implement efficient recalls and protect Americans from foodborne illness or public health hazards. More ...
On its fourth attempt to pass muster with the FDA, the company’s SPN-830, now branded as Onapgo, finally earned the agency’s stamp of approval to treat motor fluctuations in adults with ...
PAS information chief Ahmad Fadhli Shaari has sarcastically "thanked" DAP for offering to pay for lessons to educate PAS about Chinese names. However, he said it would be better for DAP to enrol ...
February 04, 2025--(BUSINESS WIRE)--Genentech, a member of the Roche Group (SIX: RO, ROG; OTCQX: RHHBY) announced today that the U.S. Food and Drug Administration (FDA) has approved Susvimo ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results