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Definition A broken jaw is a break in the jaw bone. A dislocated jaw means the lower part of the jaw has moved out of its normal position at one or both joints where the jaw bone connects to the skull (temporomandibular joints). Alternative Names Dislocated jaw; Fractured jaw; Broken jaw; TMJ dislocation Considerations A broken or dislocated jaw usually heals completely after treatment. However, the jaw may become dislocated again in the future. Complications may include: Airway blockage Bleeding Breathing blood or food into the lungs Difficulty eating (temporary) Difficulty talking (temporary) Infection of the jaw or face Jaw joint ( TMJ ) pain and other problems Problems aligning the teeth Causes The most common cause of a broken or dislocated jaw is injury to the face. This may be due to: Assault Industrial accident Motor vehicle accident Recreational or sports injury
Millions of people take bisphosphonate drugs to prevent bone loss, but do they know the risks. These medications are commonly used to treat osteoporosis, but can also cause pain, and specifically a condition called Bisphosphonate Induced Osteonecrosis of the Jaw (BIONJ). People who take a bisphosphonate need to know what BIONJ is, which drugs are most likely to cause it, who is at risk, and what to do about these risks.
What is Bisphosphonate Induced Osteonecrosis of the Bone (BIONJ)? Osteonecrosis of the bone is defined as the "presence of exposed bone in the maxillofacial (jaw) region that does not heal within 8 weeks after identification by a health care provider" according to the American Society of Bone and Mineral Research. This particular type of osteonecrosis is caused by the bisphosphonate drugs, hence the name "Bisphosphonate Induced". The common symptoms include jaw pain, swelling, infection, loosening of the teeth and drainage. Of course, seeing bone is defi...
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 decision about acetaminophen, but an FDA advisory panel has made 10 recommendations concerning the drug. Among those recommendations, the panel voted to remove acetaminophen-containing painkillers such as Vicodin, Tylenol 3, and Percocet from the nation's formularies. It also voted in favor of removing all acetaminophen-containing prescription drugs from the market. But the panel voted to keep over-the-counter (OTC) pills that combine acetaminophen and other ingredients, su...
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