On Oct. 10, the FDA classified the recalled prescription medication as a Class II recall. The risk classification from the ...
Atorvastatin (Dispitor (10 mg)) is an HMG-CoA reductase inhibitor, also known as "statin”, prescribed for hyperlipidemia. The information provided on this page is intended to serve as a comprehensive ...
The recall of a widely used statin taken by those with high cholesterol is raising more attention than recalls sometimes do.
Atorvastatin (Atorble (10mg) is an HMG-CoA reductase inhibitor, also known as "statin”, prescribed for hyperlipidemia. The information provided on this page is intended to serve as a comprehensive ...
A New Jersey-based pharmaceutical company recalled over 100,000 bottles of statin due to "failed dissolution specifications," according to the USDA.
Daily Voice on MSN
Recall Issued For Top-Selling Cholesterol Drug Atorvastatin
A drug taken daily by millions of Americans has been recalled nationwide after federal regulators said it failed quality ...
The Hill on MSN
Cholesterol medication recalled over ‘failed dissolution specifications’: What to know
The recall currently only affects bottles of 10mg, 20mg, 40mg and 80mg atorvastatin calcium tablets manufactured by Alkem Laboratories, Ltd., of India, and distributed by Ascend. The recalled bottles ...
The US Food and Drug Administration (FDA) has issued an urgent nationwide recall of more than 140,000 bottles of Atorvastatin Calcium tablets, a generic version of the popular cholesterol drug Lipitor ...
The Food and Drug Administration has announced a nationwide recall of atorvastatin calcium tablets, a generic version of the widely used cholesterol-lowering drug Lipitor, after lab tests showed the ...
Male and female patients (aged 18-80 years) with CHL were recruited from referrals to 25 hospital clinics in Spain and Portugal. An institutional review board at each centre approved the protocol, and ...
More than 141,000 bottles of a common cholesterol medication distributed nationwide have been recalled, according to the U.S. Food and Drug Administration.
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