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The Annual Report is now accessible on the SEC website at http://www.sec.gov and on the Company's website at ...
The risk for ocular problems linked to different formulations of semaglutide appear to vary, according to a new study, which ...
The rate of adverse event reporting was not significantly different between HTP ... intervention groups), BoPH and adverse event data into a predesigned and piloted form in Covidence. BoPH data ...
DUBLIN and SHANGHAI, April 28, 2025 (GLOBE NEWSWIRE) -- PDD Holdings Inc. ("PDD Holdings” or the "Company”) (NASDAQ: PDD) today announced that it filed its annual report on Form 20-F for the fiscal ...
Methods: The study included data from the FDA Adverse Event Reporting System (FAERS) spanning from the first quarter of 2004 to the first quarter of 2024. We employed the disproportional analysis ...
Photo by Alex Dodd - CameraSport via Getty Images Call it a glass-half-empty view, but in what, after all, is just my opinion among thousands of Sunderland fans, I don’t think our recent form is ...
Results showed semaglutide was the only medication implicated in 81.7% of adverse events and was most often in injectable form (94%). More than two-thirds (69.3%) of ED visits were due to ...
There is no guarantee that the expected events, trends, or results will occur ... which allows complainants to anonymously and confidentially report suspected activities that involve criminal ...
This study aimed to investigate the risk factors for drug-induced cataracts by analyzing large-scale data from the U.S. Food and Drug Administration Adverse Event Reporting System (FAERS). Methods: We ...
The US Food and Drug Administration (FDA) said Tuesday it has become aware of reports of adverse events associated with compounded topical finasteride products, and it has issued an alert for ...
If you are a vaccine recipient who has been vaccinated and have experienced an AEFI, please ask your doctor, nurse practitioner, nurse, or pharmacist to complete an AEFI form on your behalf ...
Patients worldwide suffer from high-frequency adverse events (AEs). However ... reagent and consumable errors and incorrect results in the analytical phase; delayed reporting of critical values in the ...
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