Levofloxacin

Levofloxacin is a brain and body toxic drug which is sold under a brand name of Levaquin. Johnson and Johnson also known as JNJ has a subsidiary called Ortho-McNeil which is marketing this deadly drug.
Our website has many facts which people have shared about the bad experience they had with Levofloxacin. If your planning to use Levofloxacin you could be the next victim.
Levaquin isn’t one of the drugs that you will see commercials for. However, it remains one of the most popular and frequently prescribed drugs in the world. It is a type of an antibiotic known as a fluoroquinolone. A synthetic anti-bacterial medication available only through a prescription from your doctor. With the number of fluoroquinolone prescriptions written each year, one might assume that the drug is perfectly safe for anyone to use. The truth, however, is that there are thousands of cases of Levaquin poisoning which go unreported by doctors and drug companies.
Proper Levaquin warnings have failed to reach both the medical profession and the public at large. Documentation obtained through a “Freedom of Information Act” request to the FDA revealed that there have been over 1,000 deaths that are directly attributable to Levaquin. Doctors rarely report serious adverse reactions to medications through the FDA medwatch program. Hence, the number of deaths listed above only represent a fraction of the true safety profile for Levaquin In July of 2008, the FDA mandated that all Quinolone antibiotics carry a “Black Box” warning for tendon rupture and tendonitis. A “Black Box” warning is the strongest warning label a drug can have before it is removed from the market. Public Citizen, a consumer advocacy group, sued the FDA demanding Quinolones carry a Black Box warning. On behalf of Quinolone victims in the state of Illinois, the Illinois Attorney General’s Office also petitioned the FDA on this matter. Most people do not realize that the FDA gets over 50 percent of their funding for the review of drugs directly from the pharmaceutical companies in what is called prescription drug user fees. This is a conflict of interest that has made the FDA very slow and often reluctant to react to certain drug toxicities. The FDA does not do their own rigorous studies on the safety of prescription drugs. Instead, they rely on studies submitted to them from the drug companies. Even the FDA admits that 90 percent of all adverse drug reactions go unreported to their agency through the FDA Medwatch program. Sadly, the FDA has turned a blind eye to the Quinolone tragedy.
Dr. Jay Cohen, a healthcare specialist and connect lecturer at the School of Florida, San Paul released a paper on serious side-line neuropathy caused by Quinolones. Dr. Cohen says that these incapacitating tendencies are not scarce. He says that most healthcare doctors have ignored individual grievances or overall reject that Quinolones can cause this type of lasting harm even though it is mentioned in the package place. Even if one individual in 100 goes through a burial plot side effects, that can still mean hundreds of many individuals are impacted.
Some individuals have immediate tendencies to Quinolones, others have late tendencies. The late poisoning in which symptoms reveal many weeks to months after taking the Quinolone anti-biotic is what has helped hide the high amount of people impacted. The true amount of people detrimentally suffering from this training of medicines each year is amazing. Unfortunately, many health professionals are undereducated and wrong about the problems of Quinolone medicines. Drug sales associates efficiently reduce and reduce these serious complications. Drug associates are paid a bonus on the variety of solutions written by healthcare doctors. Because of this, they often do not provide a balanced standpoint on the risk/benefit rate regarding these medicines. Most healthcare doctors are conscious of the prospective muscle harm with Quinolones, but not the serious and harmful nerve (central and peripheral) harm. It is important for healthcare doctors to try and take a more active role in training themselves about the toxic nature of this training of medicines.
Quinolones have damaged a large amount of individuals physically, on an emotional level, and monetarily. It makes a horrible stress on close relatives who have to proper take good their loved one who has been harmed by Levaquin or other Quinolones. It is also priced at people in the form of social security inability, greater health proper care costs, and lost productiveness. There are many better sessions of medicines available that should be used before a Quinolone is recommended. This training of medicines is being recommended simultaneously and without proper warning to people. People are entitled to the right to informed approval and better disclosure of the prospective permanent harm. In addition, the running of Quinolone medicines leads to greater microbe level of resistance.
Johnson & Jackson has offered Levaquin in a dangerous manner in order to increase sales. According to the FDA Independence of Information Report for Levaquin, the drug has been associated with the following unwanted events: Loss of life, Kidney Disaster, Encephalopathy, Liver wood Problem, Multi-Organ Disaster, Loss of sight, Tendon Crack, Fibromyalgia syndrome, Rhabdomyolysis, Anxious System Problem, Polyneuropathy, and Hearing problems to name a few. Jackson & Jackson has extensive been conscious of the harmful and serious accidents from Levaquin. Unfortunately, the current authority at Jackson & Jackson is fairly broke. The dreadful level of avarice by the Jackson & Jackson Board of Administrators has led to lasting suffering that could have been stopped or reduced.
If I can save one individual from having their life damaged as a result of Levaquin then this blog will have provided its purpose. I can not modify what happened to me but I can try to help modify what happens to other individuals in the future.