Latest Adverse effect Stories
A Class I recall designation by the FDA indicates that use of the recalled medical device may potentially lead to serious adverse reactions or death. Port Washington,
With the release of a recent JAMA Psychiatry study showing that psychiatric drugs send nearly 90,000 Americans to emergency rooms annually, Citizens Commission on Human Rights, the leading mental
MISSISSAUGA, ON, Sept. 8, 2014 /PRNewswire/ - Nuvo Research Inc.
RANDOLPH, N.J., Sept.
A new study and several lawsuits link Xarelto with uncontrollable bleeding injuries and increased risks of hemorrhage, stroke, pulmonary embolism, and death.
Researchers have identified genetic variants that are associated with severe adverse skin reactions to the antiepileptic drug phenytoin.
A recent regulatory filing exposes that adverse events occurred in 14% of patients taking Acthar in 2013.
The Rottenstein Law Group, a national personal injury law firm, has launched a new website dedicated to providing the public information about the dangers of Xarelto and legal options if they
MADISON, Wis., July 24, 2014 /PRNewswire/ -- Restore Health, a leading personalized medicine company that provides specialty and compounded pharmaceuticals, announced that it is now offering
TEMPLE, Texas, July 18, 2014 /PRNewswire/ -- Unique Pharmaceuticals, Ltd., ("Unique" or "the Company") today announced a voluntary nationwide recall of all sterile drug preparations compounded by the
- a slit in a tire to drain away surface water and improve traction.