Considering an Avelox lawsuit? The lawyers at Baron & Budd are currently investigating people ready to file a lawsuit for Avelox side effects, complications, and injuries. Some of the most dangerous complications we are helping people get compensation for include aortic injury (in the heart valve) after taking Avelox antibiotics. Patients have died from aortic aneurysm (rupture of the aorta) and aortic dissection (tearing of the aorta) after taking this strong antibiotic. In addition to aneurysm lawsuits, we are also accepting cases for people diagnosed with peripheral neuropathy after taking the antibiotic Avelox. Peripheral Neuropathy is a terrible form of nerve damage. Recent studies have shown that taking fluoroquinolones, like Avelox, Levaquin or Cipro can double a patient’s risk for peripheral neuropathy.
If you are not diabetic, have taken Avelox and now suffer from peripheral neuropathy, contact an Avelox lawyer at Baron & Budd at (866) 347-7765 or complete our contact form to see if you qualify for a peripheral neuropathy lawsuit.
Do You Qualify?
You may qualify for an Avelox lawsuit if you suffered an aortic anuerysm, aortic dissection, or other aortic injury after taking Avelox. People diagnosed with peripheral neuropathy nerve damage after taking Avelox antibiotics may also inquire about filing a claim for compensation. Contact an Avelox lawyer at Baron & Budd for a free confidential review of your potential peripheral neuropathy or aortic aneurysm lawsuit.
Do I Qualify for an Avelox Lawsuit?
If you suffered an aortic aneurysm or other aortic tear/injury after taking Avelox, you probably qualify to file a lawsuit against Avelox manufacturers. At this time, our firm’s Avelox lawyers are investigating cases where patients took the drug Avelox, sometimes even in combination with other fluoroquinolone drugs like Levaquin or Cipro, and were subsequently diagnosed with peripheral neuropathy. If you took either Avelox and Levaquin, or Avelox and Cipro together you may also qualify to file a claim; however, you may be eligible to file a claim against more than one manufacturer.
Though there have been previous lawsuits filed regarding the connection between Avelox, other fluoroquinolone antibiotics and aortic injury or tendon rupture, our firm is only investigating potential lawsuits for victims who sustained an aortic aneurysm, aortic dissection, or painful peripheral neuropathy issues at this time. Also, unfortunately we are only able to accept cases where the patient is not diabetic and has not taken the generic form of the drug. Read more about generic drugs and lawsuits on our blog. If you are unsure of whether you qualify, please reach out to us so that our team of legal professionals can find out if you are entitled to compensation from an antibiotic side effect lawsuit. We want to help.
What is Peripheral Neuropathy?
Peripheral Neuropathy is the medical term fora specific type of nerve damage that can be temporary or permanent. The condition is characterized by weakness, nerve pain, unexplained clumsiness and loss of coordination, and joints that lock-up with numbness. This type of nerve damage can affect every minute of someone’s day; life with Peripheral Neuropathy is not easy.
How Long Does it Take to Get Peripheral Neuropathy from Avelox?
Symptoms of peripheral neuropathy can begin the first day of taking Avelox, or within 24 hours. However, the danger of developing peripheral neuropathy does not go away after you have finished the course of antibiotics; people who have taken Avelox and other FLQs can still develop peripheral neuropathy at least 180 days after taking it. Most people start experiencing symptoms of neuropathy within a week of taking Avelox, so know the symptoms and alert your doctor immediately if you experience any of them.
Peripheral Neuropathy Symptoms to Watch Out For Include:
- Tingling, Burning Sensation (most commonly occurring in the legs and arms)
- Sharp Cold or Hot Nerve Pain in the Hands and Feet
- Tingling Numbness that Locks Joints in Place
- Lessened Pain Sensitivity
- Muscle Loss or Weakness
- Loss of Motor Skills & Coordination
- Sensitivity to Light
- Decreased Mobility ( in severe cases the inability to walk or stand)
These are just a few of the symptoms caused by this debilitating nerve damage. If you are experiencing some of these indications, please study a more comprehensive list of Peripheral Neuropathy symptoms to see if you should contact a doctor and/or attorney.
How Long After Taking Avelox Does it Take to Develop an Aortic Injury Such as Aneurysm, Dissection, or Tearing?
Aortic injury after Avelox treatment can occur as soon as one week after starting Avelox, but can begin as long as seven to 10 years after the course of antibiotics is completed. That is because Avelox weakens the lining of the aortic valve over time and there is no set number of days after starting treatment that the tissue weakens to the point of tearing or bulging. The deterioration can occur slowly or happen quickly, with acute anuerysm occurring just days after treatment starts. For this reason, it is imperative that you reach out to your physician immediately if you experience any symptoms of an aortic injury.
Aortic Aneurysm Symptoms Include:
- Sudden, Intense Pain in Lower Back and/or Abdomen
- Ripping Sensation in the Chest
- Consistent Pain After Sudden Pain Radiating Through Torso, Legs
- Feeling as Though Something is Tearing Inside Abdomen or Lower Back
- Shortness of Breath
- Low Blood Pressure
If you have any of these symptoms and have taken Avelox or any other FLQ antibiotic recently, call your doctor immediately. If you are having a medical emergency and experience these symptoms with low blood pressure, consider contacting emergency services.
Symptoms of Aortic Dissection
- Sudden Weakness or Paralysis on One Side of the Body
- Loss of Pulse on One Side of Body
- Chest Pain
- Lower Back and/or Abdominal Pain
- Nausea, Vomiting
If you are experiencing symptoms of aortic dissection, which could include tearing or separation of the aortic valve lining, you should seek medical attention right away. Aortic dissection can be fatal, and internal blood loss can go undetected until it’s too late if you ignore the signs. If after seeking medical treatment you are diagnosed with aortic dissection, seek legal counsel from an experienced lawyer at our firm who can see if you qualify for an Avelox aneurysm lawsuit or claim for aortic valve injury compensation.
Why File an Avelox Lawsuit?
You should file an Avelox lawsuit to make the drug’s manufacturers pay for not disclosing the potentially deadly and chronic side effects of the drug on the warning label. 50% of aortic aneurysms are fatal, and aortic tearing and dissection can lead to life-long health complications requiring continued medical care. Peripheral neuropathy can completely change your life as well. And, sadly, not for the better. Recent studies have revealed that taking a fluoroquinolone drug like Avelox can double your risk of developing peripheral neuropathy or suffering an aortic injury. Doctors prescribing the antibiotic, as well as patients who take it, were not aware of the dangerous nerve damage side affects of Avelox. Filing an Avelox lawsuit can:
- Send a message to the drug companies, telling them that they were wrong.
- Help prevent others from also suffering from peripheral neuropathy related to Avelox use.
- Help prevent other people from fatal aortic aneurysm, dissection, or tearing in the aortic valve.
- Help you get compensation and additional funds to help pay costly medical bills, provide for any long-term medical care and help make up for lost income because of your inability to work.
Avelox is the brand name for the drug moxifloxacin, a broad-spectrum antibiotic used to treat different types of bacterial infections.
From bacterial skin, lungs, sinus, or stomach infections, Avelox works by stopping the growth of bacteria in the body. It does this by disrupting DNA replications and cell division within bacteria.
Avelox belongs to a class of antibiotic drugs known as fluoroquinolones, or quinolone antibiotics, which is a fancy way of saying that Avelox is part of a very, very strong antibiotic group of drugs that can be used to treat different bacteria strains. In addition, broad-spectrum antibiotics like Avelox are often prescribed to treat symptoms caused by concurrent bacterial infections, or to treat undetermined life-threatening bacterial infections like meningitis, or to treat bacterial infections when other antibiotics have failed.
Experts advise that quinolone antibiotics such as Avelox only be prescribed as a last resort to patients with bacterial infections. This is for a number of reasons. One, because Avelox and other quinolone antibiotics are so strong, they are only needed to treat life-threatening conditions. Two, because taking a strong antibiotic such as Avelox over time may render the patient less likely to respond to the same antibiotic in the future (and when they may really need it for a life-threatening condition!). Three, because Avelox may interact with other drugs and even herbal supplements.
However, last resort-scenario or not, quinolone antibiotics such as Avelox are among the most prescribed antibiotics in the United States. What that means is, all too often, quinolone antibiotics like Avelox are prescribed for conditions for which they are not approved or conditions that are not life-threatening to the patients. In particular, Avelox is often marketed for patients with common respiratory tract infections.
Unfortunately, use of Avelox also comes with a cost: the fourth reason why Avelox and other quinolone antibiotics should only be prescribed for life-threatening conditions.
Reason number four is the associated risk of permanent peripheral neuropathy, a type of nerve damage that can be debilitating to patients and that can occur quickly after the patient first starts taking Avelox.
The fifth reason that these strong antibiotics should only be considered as a last resort is the risk of fatal aortic injuries including aneurysm of the aortic valve, tearing of the aorta, and separation of the aortic vein’s lining.
Peripheral neuropathy is the medical way of saying nerve damage. Sometimes peripheral neuropathy occurs in older patients who are suffering from diabetes or other conditions that involve a risk for developing peripheral neuropathy. However, peripheral neuropathy has also been associated with the use of the antibiotic Avelox.
The peripheral nervous system is composed of three main types of nerves: autonomic nerves, sensory nerves and motor nerves. Each of the three types of nerves has its own function.
Autonomic nerves help control the automatic functions of the body like bladder function and blood pressure.
Sensory nerves help the body signal sensations such as pain and temperature from the affected region of the body to the brain.
Motor nerves help control the muscles of the body.
So, if the peripheral nervous system becomes damaged, one may suffer symptoms in their sensory nerves such the feeling of numbness or tingling in the hands and feet or a burning or shooting pain, or they may suffer symptoms in their motor nerves such as the loss of coordination or severe muscle weakness.
But most often, those suffering from the nerve damage known as peripheral neuropathy suffer a variety of symptoms — all relating to the damage of the autonomic, sensory and motor nerves. In fact, over 100 symptoms have been associated with peripheral neuropathy.
Typically, patients suffering from peripheral neuropathy experience the worst symptoms in their arms and legs. Some of the most common symptoms of peripheral neuropathy include weakness, numbness, tingling, burning, pain or a change in sensation to temperature, light, touch or sense of body position.
The nerve damage can be so severe or long-lasting that some patients with peripheral neuropathy may be unable to work because of a loss of motor skills or may experience other significant trauma in their life and work because of the severe tingling, pain or change in sensation.
For those suffering from peripheral neuropathy caused by Avelox, the peripheral neuropathy may occur immediately after the patient first starts taking the antibiotic. Unfortunately, once the peripheral neuropathy occurs, it may continue for weeks, months, years or even persist for the rest of the patient’s life.
For this reason, patients who experience peripheral neuropathy while taking Avelox are advised to contact their doctor as soon as symptoms occur.
The associated risk between quinolone antibiotics like Avelox and peripheral neuropathy was reported by researchers as early as 2001. The peer-reviewed journal the Annals of Pharmacotherapy noted that the symptoms of peripheral neuropathy may occur quickly in patients.
When do Symptoms of Neuropathy Most Often Occur?
- 33% of patients may experience peripheral neuropathy symptoms within the first 24 hours
- 58% of patients may experience peripheral neuropathy symptoms with the first 72 hours
- 84% percent of patients may experience peripheral neuropathy symptoms within the first week of taking Avelox or other quinolone antibiotics.
Importantly, this paper also noted that, for many patients, the peripheral neuropathy did not go away once the patient stopped taking the fluoroquinolone.
The FDA issued a Safety Announcement in August 2013 that advised doctors and patients that it was requiring a label change to Avelox and other quinolone antibiotics in order to make sure that the serious risk of potentially irreversible peripheral neuropathy was clearly expressed.
According to the Safety Announcement:
“This serious nerve damage potentially caused by fluoroquinolones may occur soon after these drugs are taken and may be permanent … It can occur at any time during treatment with fluoroquinolones and can last for months to years after the drug is stopped or be permanent.”
Avelox has not only been linked to tendon ruptures, tendonitis and other potentially debilitating conditions, this powerful antibiotic may also increase a patient’s risk of damage to the aorta. Studies published in the Journal of the American Medical Association (JAMA) as well as the British Medical Journal (BMJ) show that patients taking Avelox and other fluoroquinolones are at a substantially increased risk of aortic aneurysms (bulges) and dissections (tears in the aortic wall).
In the JAMA study, Taiwanese researchers studied the medical data of nearly 1,500 patients who has suffered an aortic aneurysm after taking Avelox or another fluoroquinolone. They found that the patients were 2.4 times more likely to develop an aneurysm within 60 days of taking the antibiotic. The patients were twice as likely to suffer this complication if they had used fluoroquinolones in the past.
The BMJ study was performed by Canadian researchers who looked at the health records of approximately 650,000 patients. They determined that patients who took fluoroquinolones were at triple the risk of suffering an aortic injury.
Approximately 15,000 people die due to aortic aneurysms each year. Many people do not know they have this problem until it bursts. Warning signs include:
- Constant or occasional abdominal pain
- Lower back pain that radiates to the buttocks, groin or legs
- A pulsating sensation in the abdomen similar to a heartbeat
If you take Avelox or any other type of fluoroquinolone, please have a doctor examine you for any potential aortic injuries.
Avelox was developed by the German pharmaceutical giant Bayer AG and is marketed by Bayer’s partner Schering-Plough Corporation. Initially, Avelox was brought to the market by Bayer with the intention of replacing one of Bayer’s other popular quinolone antibiotics, Cipro. However, Cipro was left on the market and Avelox became another source of revenue for Bayer — and a big one, at that.
In 2007, sales of Avelox made $697.3 million in revenue worldwide. Today, Avelox sales equal roughly $500 million per year.
Despite the known risks associated with Avelox and other quinolone antibiotics, Bayer was not forthright with the risks and side effects for way too long — for both their bestseller Cipro antibiotic and for Avelox.
In fact, the FDA’s response to the dangers of quinolone antibiotics is largely a result of the actions of patients who have been injured and formed together to seek action. In 2006, the national nonprofit consumer advocacy organization known as Public Citizen asked Bayer to more strongly warn doctors and patients about the risk of tendon rupture associated with quinolone antibiotics. At the time, quinolone antibiotics were blockbuster drugs and Bayer was making millions off of both Avelox and Cipro.
Unfortunately, Bayer refused to listen to Public Citizen in 2006. And that’s when the FDA finally had to step in, issuing the most stringent warning, the “Black Box” warning, for all quinolone antibiotics in 2008. However, the warning did not include the severe or permanent risk of peripheral neuropathy. The FDA finally alerted doctors and patients of the risk of peripheral neuropathy for both Avelox, Cipro and other quinolone antibiotics in 2013.
The responsibility of hearing of a drug’s associated risks and side effects should fall on the manufacturer and marketer of the drug. When the drug’s manufacturer and marketer fail to properly warn patients, then the FDA has to take charge (and yes, the FDA’s process is sometimes slower than we would like).
However, there are some drugs that get attention outside of the FDA or the necessary label warnings. That attention is often from the media and for some quinolone antibiotics like Levaquin, there was a significant amount of press over the last couple of years, much of it surrounding the risk of tendon rupture or damage.
However, while the quinolone antibiotics Avelox have the same basic chemical structure of Levaquin (also a quinolone antibiotic), little has been done to draw public attention or education to its risks. Unfortunately, many patients who took Avelox and developed symptoms of peripheral neuropathy were completely blindsided by the symptoms — they really had no idea that the risk was a possibility at all.
The lack of public knowledge would be a problem for any drug with dangerous side effects or risks, but for Avelox, the problem is even bigger because of the difficulty that may come with identifying the symptoms of peripheral neuropathy in patients.
All too often, patients suffering from peripheral neuropathy report their symptoms to muted ears. Because Bayer did not make the risks of peripheral neuropathy as clear as they should have, the medical field was unprepared to recognize the symptoms once they started occurring in patients. And for that reason, some patients who suffered symptoms of peripheral neuropathy were told something that they should have never been told: they were told it was in their heads, that their symptoms were not real. We now know that their suffering was real, and victims may be entitled to file a lawsuit for serious injuries and fatalities.
A great deal has been done by the FDA to expose the damage Avelox is capable of causing.
In October 2008, the FDA placed the most serious alert on Avelox and other quinolone antibiotics, known as a “Black Box” warning. The label warned doctors and patients of the serious risk of tendon damage that comes with taking Avelox and other quinolone antibiotics.
Then, in August 2013 the FDA updated its Safety Announcement to alert doctors and patients of the risk of serious and permanent peripheral neuropathy that may occur soon after patients first start taking Avelox.
However, despite the warnings, there has been no ban or recall of Avelox.
What that means is that, despite the countless individuals who have already been harmed by Avelox and other quinolone antibiotics, even more patients may be seriously or fatally injured in an aortic rupture or aneurysm, or suffer from peripheral neuropathy at the hands of Bayer’s Avelox. Contact our office today to speak with an attorney about filing an Avelox nerve damage lawsuit.