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1 小时
FDA Issues Urgent Warning on Dangers of Common Dog Medication
The United States Food and Drugs Administration is warning pet owners about a common medication given to pets to treat ...
1 天
FDA Issues Vet Letter on Drug Librela Used to Control Pain in Dogs
The FDA's Center for Veterinary Medicine posted a letter alerting veterinarians of adverse health effects in dogs from ...
3 天
FDA Issues Warning About Potentially Deadly Side Effects From Pain Drug For Dogs
The FDA's Center for Veterinary Medicine now is reporting a series of adverse events related to the drug. They include ataxia, seizures and other neurologic signs. Those include paresis, recumbency, ...
10 小时
FDA expands approval of Vtama to include atopic dermatitis
The U.S. Food and Drug Administration has approved Organon's Vtama (tapinarof) 1% cream for an additional indication -- the ...
todaysveterinarybusiness
3 天
Zoetis Responds to FDA’s ‘Dear Veterinarian’ Letter
The FDA has issued a “Dear Veterinarian” letter notifying practitioners about adverse events reported in dogs treated with ...
6 小时
Popular Dog Medication Could Have 'Dangerous Side Effects' for Pups, Warns FDA
The warning was issued for Librela, which is a painkiller commonly given to dogs to relieve arthritis pain. The drug is ...
1 天
Dog pain medication linked to illness, death, FDA warns
(WDBJ) - The U.S. Food and Drug Administration has issued an alert to veterinarians about a popular medication used to ...
12 天
on MSN
Spice Recall Update as FDA Sets Most Serious Risk level
"People who have an allergy or severe sensitivity to soy and wheat run the risk of serious or life-threatening allergic ...
Joplin Globe
4 小时
U.S. FDA Approves Pfizer’s BRAFTOVI® Combination Regimen as First-Line Treatment of BRAF ...
U.S. FDA Approves Pfizer’s BRAFTOVI® Combination Regimen as First-Line Treatment of BRAF V600E-Mutant Metastatic Colorectal Cancer ...
Too Old to Operate
9 天
Adverse Events in Cancer Therapy With Antibody-Drug Conjugates
The Toxicities and Adverse Effects That Emergency Physicians Must Know,” published in the December 2024 issue of Emeregency ...
3 天
Tonix Pharmaceuticals Announces FDA Acceptance of the New Drug Application (NDA) for TNX ...
FDA is expected to assign a Prescription Drug User Fee Act (PDUFA) target action date and announce whether Priority Review has been granted in ...
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