Levaquin Linked To Tendon Ruptures
Between 1989 and 1999 Medical Journals Have Reported 100 Cases of Levaquin Tendon Ruptures:
The antibiotic Levaquin has been reported to weaken tendons, which can rupture under heavy physical stress. Levaquin side effects may leave patients incapacitated, needing serious surgeries and months of rehabilitation. These patients are also faced with expensive medical bills. The areas of the body most affected include the Achilles' tendon, knee, and rotator cuff. Athletes or individuals who have workloads that put a lot of pressure on their joints are more apt to experience Levaquin side effects. It has been reported that 100 million Levaquin prescriptions have been written in the United States between 1989 and 1999, with 100 cases of Levaquin tendon ruptures reported according to medical journals. Medical journals have reported that Levaquin tendon ruptures may occur after 7 to 14 days of treatment, but may also occur after treatment ends. The risk of Levaquin side effects may increase the longer you remain on this therapy.
Petition by Illinois Attorney General Links Levaquin to Tendon Rupture:
The Illinois Attorney General and a consumer advocacy group filed a petition against the FDA in 2005, requesting that a black box warning be added to Levaquin advertisements regarding the risk of tendon ruptures. The petition stated that Levaquin tendon ruptures continued to occur at an alarming rate. The petition also stated that many tendon ruptures could be prevented if doctors and patients were aware of the early warning symptoms associated with tendon ruptures. Because the FDA declined the petition, a Levaquin lawsuit was filed against the FDA in an attempt to force the agency to order a black box warning regarding the increased risk of tendon rupture in patients taking Levaquin. In July 2008, the FDA was ordered to notify manufacturers of Levaquin to add a black box warning to the prescribing information about the increased risk of developing tendonitis and tendon rupture. Manufacturers are also required to create a guidebook that will be provided to all patients to warn them of the risks of Levaquin side effects.
If you have taken Levaquin and have suffered from tendonitis, tendon rupture, or other Levaquin side effects, you may want to consult a Levaquin lawyer to see if you qualify for a Levaquin lawsuit.
Questions and Answers
Levaquin is a synthetic antibiotic used to treat bacterial infections. A number of side effects have been reported that include tendonitis, peripheral nerve damage, liver damage and convulsions. In 2008, the manufacturer Johnson & Johnson was required to place a black box warning on all of their packages.
Levaquin, an antibiotic, used to treat bacterial infections has been linked to a number of studies suggesting the prescription drug's side effects may be severe. One of the alleged side effects includes tendon rupture, that some have said may cause permanent damgage or require surgery to repair.
The FDA approved Levaquin, an antibiotic used to treat patients with bacterial infections, in 1996. The FDA has had to revise Levaquin's safety label on numerous occasions due to serious side effects.
Despite serious warnings from the FDA and a Black Box warning label, the risk of a Levaquin-caused tendon rupture is still a frightening reality for many taking the medication.
Levaquin is an anti-bacterial medication used on an array of bacterial infections from pneumonia to chlamydia. Reports have surfaced regarding the severe side effects associated with taking the drug including tendon rupture that may cause surgery to fix.
If you are one among the many thousands of teenagers or adults that suffer from acne infections on your torso, you have probably been looking for information on how to eliminate acne on your back. Large and aching cysts under the skin, general tenderness and redness and even pus filled pimples and sores are all signs of acne on your back. This condition is usually called bacne to differentiate it from face acne.
Nobody wants to be spotty. It is a universal truth. Regardless of how old we become--bad skin, be it the rare zit or full blown acne--is shameful. Acne, in particular, can be a problem for us for much longer than we had counted on when we first entered puberty as young adults. For a long time we've covered our faces with high-priced chemicals and products hoping to keep the acne far from us. But what if you could clear up your skin in much easier and less harmful ways?
No one really wants to be affected with zits. It really is just the simple truth. It doesn't matter how old we become, zits, pimples, acne -- terrible skin in whatever form it takes -- is embarrassing. Acne, in particular, can be a plague for us for considerably longer than we had counted on when we first entered puberty as young adults. We spend years slathering ourselves with every chemical and acne fighter we can find.
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Acne Vulgaris or commonly known as acne is a skin illness usually appears during our teenage years when one's hormones and skin oil glands are most productive. It may result in a great deal of changes not just in a person's physical appearance but psychologically at the same time.
Fosamax, an osteoporotic drug manufactured by Merck, has been linked to bone damage including a rare femur fracture and osteonecrosis of the jaw (ONJ) as well as a number of other side effects.
Fosamax (a bisphosphonate) is a prescription drug used to treat osteoporosis. This drug has been linked to a rare femur fracture. Other Fosamax side effects include atrial fibrillation, joint and/or muscle pain and bone necrosis of the jaw (ONJ) to mention a few. The FDA has issued an alert to healthcare professionals to monitor patients for these side effects.
The orthopedic subsidiary of Johnson and Johnson, DePuy, has recalled two of its hip replacement systems due to a high failure rate. DePuy is offering an early hip replacement settlement. Meanwhile, a motion for a hip replacement class action lawsuit as well as many individual hip replacement lawsuits have been filed.
The medical device subsidiary of Johnson and Johnson, Depuy Orthopaedics has issued a Hip Replacement Recall on two of their hip replacement devices. This DePuy hip recall includes the DePuy ASR Hip Resurfacing System and the ASR XL Acetabular Cup System. This recall is due to a high failure rate that requires patients to have a second hip replacement. DePuy asks healthcare providers to monitor these patients more closely.
The DePuy ASR hip Resurfacing System and the ASR XL Acetabular System have been recalled. DePuy is offering a hip replacement settlement for this recall. A hip replacement class action has been filed for these two DePuy systems. Before contacting DePuy about compensation, you might want to contact a hip replacement attorney to make sure your rights are protected.
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