What exactly is a "black box" warning?
Simply put, it's the strongest warning that the U.S. Food and Drug Administration (FDA) can require on a drug's packaging. The FDA requires the black box warning when studies suggest a drug can cause a serious or life-threatening side effect. The text of the warning is set apart from other information in a black box, so that doctors, pharmacists, and patients can easily see it.
What did the FDA advisory panel recommend?
The FDA itself hasn't made a...
An FDA Advisory Committee recently recommended some changes regarding the use and availability of the very common pain medicine... Read more »
Yesterday the U.S. Food and Drug Administration announced that it is asking manufacturers of prescription combination products that contain... Read more »
In recent months, several news stories have been published that indicate there appears to be a link between acetaminophen and asthma.... Read more »
Qualitest, a subsidiary of Endo Health Solutions, has issued a voluntary nationwide recall for 101 lots of Hydrocodone Bitartrate and... Read more »
It is disturbing that as we enter peak cough, cold and flu season, we are faced with the dilemma that acetaminophen (sold under the brand... Read more »
The U.S. Food and Drug Administration (FDA) is warning consumers not to purchase or consume Zimaxx, Libidus, Neophase, Nasutra, Vigor-25, Actra-Rx,... Read more »
Source: ADAM Encyclopedia
Acetaminophen (Tylenol) and codeine is a prescription pain medicine. It is a narcotic, which means it has the potential to relieve pain while making... Read more »
Source: ADAM Encyclopedia
Acetaminophen overdose is one of the most common poisonings worldwide. People often think that acetaminophen, a pain-relieving medicine, is extremely... Read more »
Source: ADAM Encyclopedia
Hydrocodone and acetaminophen overdose occurs when someone accidentally or intentionally takes more than the normal or recommended amount of a... Read more »