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CBC Online 1380 KCIM
47 分钟
FDA seeks to pull common but ineffective OTC cold medicine ingredient off the market
The Food and Drug Administration (“FDA”) said on Thursday that they will seek to pull the common ingredient phenylephrine off ...
17 小时
After decades, FDA finally moves to pull ineffective decongestant off shelves
In a long-sought move, the Food and Drug Administration on Thursday formally began the process of abandoning oral doses of a ...
health enews
1 天
Nasal congestion on one side? You may have this condition
A deviated septum occurs when you have two different-sized nasal passageways which can cause one-sided congestion.
来自MSN
16 分钟
Amgen, AstraZeneca post Phase 3 win for nasal polyps therapy
Citing topline data from their Phase 3 WAYPOINT trial, the companies said that the antibody therapy reduced the size of nasal ...
Daily Voice Middlesex County NJ on MSN
1 小时
These Over-The-Counter Decongestants Don't Work, FDA Says
A common ingredient found in most oral over-the-counter cold medicines should be removed from the market because it doesn’t ...
15 小时
U.S. FDA proposes ending use of popular decongestant present in cold medicines
The U.S. Food and Drug Administration has proposed to remove oral phenylephrine, widely used in cold and cough syrups, as an ...
NBC News on MSN
17 小时
FDA proposes ending use of decongestant found in many cold, allergy medicines
The agency said an extensive review of available data determined that the ingredient, oral phenylephrine, doesn’t actually ...
3 小时
on MSN
FDA proposes ending use of popular decongestant present in cold medicines
The US Food and Drug Administration has proposed to remove oral phenylephrine, widely used in cold and cough syrups.
4 小时
TEZSPIRE MET BOTH CO-PRIMARY ENDPOINTS IN PHASE 3 TRIAL FOR CHRONIC RHINOSINUSITIS WITH ...
Amgen (NASDAQ:AMGN) and AstraZeneca today announced positive top-line results from the Phase 3 WAYPOINT trial in patients ...
The Financial Express
4 小时
USFDA proposes removal of common decongestant from shelves after finding it ineffective
The FDA would provide manufacturers with appropriate time to either reformulate drugs containing oral phenylephrine or remove ...
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