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A drug recall removes a prescription or over-the-counter drug from the market. Drug recalls in the United States are made by the FDA or the creators of the drug when certain criteria are met. When a drug recall is made, the drug is removed from the market and potential legal action can be taken depending on the severity of the drug recall.
Approved indication for dihydrocodeine is the management of moderate to moderately severe pain as well as coughing and shortness of breath. As is the case with other drugs in this group, the antitussive dose tends to be less than the analgesic dose, and dihydrocodeine is a powerful cough suppressant like all other members of the immediate codeine family (see below) and their cousins ...
Drugs or medicines may be withdrawn from commercial markets because of risks to patients, but also because of commercial reasons (e.g. lack of demand and relatively high production costs).
The FDA proposed a ban on phenylephrine, a common decongestant found in cold and cough medications. Here’s why and a list of medicines with phenylephrine.
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Certain MadeGood granola bars sold nationwide by retailers including Amazon and Walmart are being recalled because they may contain pieces of metal, Riverside Natural Foods said in a notice posted ...
For all questions regarding this recall, you can contact Inmar at 877-890-0765 on Monday through Friday from 9 a.m. to 5 p.m. ET or by email at rxrecalls@inmar.com.
In medicinal chemistry, the term "contamination" is used to describe harmful intrusions, such as the presence of toxins or pathogens in pharmaceutical drugs. [1]The following list encompasses notable medicine contamination and adulteration incidents.