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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Drugs or medicines may be withdrawn from commercial markets because of risks to patients, but also because of commercial reasons (e.g. lack of demand and relatively high production costs).
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 ...
Krusteaz Belgian Waffles. Costco’s recall also includes Krusteaz Belgian Waffles in 24-count packages, supplied by TreeHouse Foods. Although no specific lot number was provided, TreeHouse Foods ...
Voters in Los Banos have overwhelming voted yes to recall two city council members according to the ... Election results show 1,344 yes votes or 72.85% against 501 no votes of 27.15% of the total ...
Bluelight is a web-forum, research portal, online community, and non-profit organization dedicated to harm reduction in drug use. [1] [2] Its userbase includes current and former substance users, academic researchers, drug policy activists, and mental health advocates.
Schedule 2 (S2) drugs and poisons, otherwise known as Pharmacy Medicines, are substances and preparations for therapeutic use that – are substantially safe in use but where advice or counselling is available if necessary;