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What Fluoroquinolone Peripheral Sensorimotor Neuropathy Looks Like

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Washington, DCIt’s little wonder the US Food and Drug Administration (FDA) is in the throes of taking a good hard look at fluoroquinolones (FQs) and their association with Peripheral Sensorimotor Neuropathy. An important Canadian study appearing in late September in the Journal Neurology has the medical community talking. With headlines screaming “FDA Evaluating Fluoroquinolone Antibiotics,” it’s no surprise that everyday consumers are talking too, given that antibiotics such as Levaquin and Cipro are oft-prescribed for a wide variety of serious infections.

Dr. David Perlmutter is referencing the study found in the September 30, 2014 edition of Neurology. “Oral fluoroquinolone use and risk of peripheral neuropathy: A pharmacoepidemiologic study” was undertaken by a Canadian-US research team led by Dr. Mahyar Etminan, PharmD, of the University of British Columbia. The study authors concluded that “current users, especially new users of FQs, are at a higher risk of developing PN. Despite the increase in the use of FQs, clinicians should weigh the benefits against the risk of adverse events when prescribing these drugs to their patients.”

It’s a sobering thought, especially since at one time the primary concern with fluoroquinolones were Cipro tendon rupture and Levaquin tendon rupture.

Not any longer. This is something bigger. It’s especially compelling when we consider the reliance we have placed on antibiotics in a society that moves so fast; with the modern workday having evolved over time from the classic nine-to-five staple to a 24/7 availability, no one has time to be sick and allow an ailment to work its way through.

Yes, serious infections such as a urinary tract or upper respiratory tract infection can be serious if left untreated. Fluoroquinolones do a very good job of eradicating serious infections. However, the concern that patients are asking for antibiotics like they were candy - with doctors over-prescribing robust antibiotics such as Cipro and Levaquin in many cases, as Dr. Perlmutter suggests - only serves to exacerbate the problem and may be exposing patients to potential serious adverse reactions like Fluoroquinolone Peripheral Sensorimotor Neuropathy unnecessarily.

The Etminan et al study noted that the risks for developing Fluoroquinolone Peripheral Sensorimotor Neuropathy doubles when compared with those study participants who were not exposed to fluoroquinolones.

So what does Peripheral Sensorimotor Neuropathy look like?

In this video under the auspices of University College Dublin, School of Medicine & Medical Science Educational Innovation, in conjunction with St. Vincent’s Healthcare Department of Neurology, Professor Niall Tubridy introduces us to Michael, who appears to be a middle-aged man with Peripheral Sensorimotor Neuropathy.

There is no reference as to what causes his Peripheral Neuropathy - Type 2 diabetes or fluoroquinolone use. However, there is little doubt that Fluoroquinolone Peripheral Sensorimotor Neuropathy is devastating to anyone who leads an active lifestyle, or who requires strength and coordination for his or her livelihood.

Little wonder consumers, who claim not to have known about the possibility of Fluoroquinolone Peripheral Sensorimotor Neuropathy, are seeking compensation through the courts. The FDA added a boxed warning to fluoroquinolones in 2008 for tendon rupture. The FDA had to revisit the warning pathway for FQ given recent revelations.

Victims of Fluoroquinolone Peripheral Sensorimotor Neuropathy have to wonder why this wasn’t identified during the clinical trial process prior to the approval of fluoroquinolones - and if it was, why consumers were left in the dark.


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Posted by

I am not good on the Internet
It would take all day of pain as when I type something
I loose it
I need someone to talk to in the same painful
Situations. As I have all poly peripheral neuropathy
On. Fire tail bone. Some much more
I am a Christian. Are we allowed to get phone numbers
As I really need to speak with some with the same problems

Posted by

Coping with Nerve Pain, Tingling, Weakness, Depression
written originally August 2003 (updated September 2007
Coping With Peripheral Neuropathy: How to handle stress, disability, anxiety, fatigue, depression, pain, and relationships
. I cannot even have a normal conversation with people because my body feels like it's ready to explode. Nothing has helped me. I am suffering in misery as of 2003
. I have suffered with chronic pain and stiffness since 2004 due to . My condition worsened. In 2006 I was diagnosed with neuropathy polyneuropathy more than 1 nerve damage in the central never stems ), stenosis by 2008 received disability thank you God I was running out of savings 2009

As of September if 2012 I am a mess. My arms burn inside like they're on fire. My backside I have agonizing toothache-like . sharp radiating, stabbing, pain all so down my right leg and right arm. I am sad from the medications. I fight depression on a daily basis. I hardly ever have the motivation to do anything anymore. I feel bad about myself. I don't want to live like this. Yet I find strength I don't have a social life, at all. I can't . Be around people because I am so irritable. People understand. The panic when I tell them how messed up I am, like they need to do something but don't know what, so the feel bad for me . This is hell on earth I assure you. There's nothing that anyone can do to help me. No one seems to care. Most-doctors don't understand that pain, I am going to explode with tension), and nerve damage—can cause a person to become depressed, irritable, have mood swings, fatigue, anxiety, and a feeling of utter hopelessness and of being overwhelmed I went through all of that. I lost my ability to work. My quality of life . I lost the desire to have fun alone without a soul in the world by my side. I wanted to scream , and would have if it weren't for my faith in God.
I don't understand life at times, but I do understanding (that only comes from casting all my cares upon the Lord. I pray for the Lord to help me

look normal, but I feel burning from head to toe at times, sharp pain radiating down the entire backside of my body. Both of my arms feel puffed-up, but my right arm feels twice it's normal size. My right leg feels half-asleep all the time. My backside feels like I have agonizing toothache-like pain in the bony area of the backside with chronic tension. My backside pain radiates into my back area and make it them feel sore. The backside pain by itself is absolutely debilitating, making me want to die and go to Heaven. I take 30 mg oxmorfein 2 times a day 10 mg oxcodine 2times Gabapentin 300mg 3 times a day metaxalone 800 mg 3times a day lyrica 150mg 2 times a day duloxetine hcl 60mg one time a day folic acid 1 mg daily and praise God for it, because without it I cry in pain and cannot survive. Yet the medications adversely affect me.
How in the world am I supposed to enjoy my meal, carry on a conversation, and live normally? I try, but my body is afflicted. I live alone because of all this, and it is lonely often. It is my burden, the cards I have been dealt in life, and I can only cope daily with God's help. The legs arms backside pain is so bad as I am typing, which is why I am typing, it helps me to preoccupy my mind. Why do you think this website is so long I've had increasing horrible pain in both hands lately.
If you are suffering from neuropathy, stenosis, and radiculopathy like I have been since 2004, my heart goes out to you. I do understand. I have no real social life because of my bodily afflictions. At times my condition is bearable, and at other times unbearable truth, fighting against tyranny and corruption, and defending liberty and freedom.Thank you for those who pray for me regularly I love you all in the Lord whoever you may be!
I ask for the continued prayers of my web visitors. I've felt overwhelmed lately from my health afflictions. I saw the picture to the left and immediately my mind said, “That's it! That's exactly how I feel inside my body. That's it!” Peripheral Neuropathy is a horrible thing to suffer, which causes daily spasms of burning throughout my nervous system, intermittent sharp radiating pain in my arms and legs, aching pain from head-to-toe and overwhelming fatigue that causes me to have to take some medications and rest. In my bed amount 24 hours a day
I'd love to go places but due to my afflictions. I am not a by nature. I went out to eat last night, which I do. I asked if I could sit on the outside,sit because of my suffering and didn't want to be feeling pain around people. The burning, tingling, pain and backside tension in all overwhelm me at times, as last night. I have a noticeable backside pain when I walk or sit down If I walk for a while it's not as noticeable.arthritis-in my hip I will get a operation in March. Or April 2016 It's when I sit down and then get back up that my leg backside harms and hands do not want to move.
I ordered a turkey and cheddar sandwich with some potato soup. I ate the soup and only half of my sandwich. I just didn't feel too well. I felt like crying. I tried to shift in my chair due to the radiating pain from my backside down my right leg. It feels like a razorblade is passing across my nerves (from my shoulders down my right arm and leg) into my finger and toe. And then there's the chronic tension inside my feet which feels like the backside is being ripped out. It never goes away. It feels like a golfball is stuck in my backside for the constipation , ready to burst out. I have constant toothache-like pain (where the bone is located in backside )which radiates into my arms area. The other night it felt like a knife was stabbing me down side of my legs my right side feels sore all over continually. The pain radiates from my toes upward. Makes me irritable understandably. If that wasn't enough to endure, then there's the burning, tingling and both of my arms feeling like swollen air-bags all the time I am trying to get a scooter I need extra money
I just have to be careful not to allow my sufferings to overwhelm me with grief and depression. I have a ministry of suffering.
People sometimes get nervous when they sense that I'm suffering, because they don't know what to say or do. There's nothing they can do. I used to try to break the tension by telling people that I have Peripheral Neuropathy. I said that one day and a married couple in their 50's literally took two-steps backwards. That hurt. I don't have Bubonic Plague! They sincerely didn't know what that term meant, so I don't use it anymore. So then I started telling people that I have a damaged spinal cord, but that freaked some people out. So now I just tell people that I have a messed up never damage This is betteThese are heavy burdens I carry, but the Lord promised that He wouldn't give us more than we can handle
in my life, Like a pregnant woman in travail, I had so much to tell the world. My problems started in March of 2003 At that time my website was still very small but by the end of 2013 this website took off and hasn't stopped growing in popularity since
(as infamous or famous as it may be). I have found out about
The devastating pain that I went through in one week than I had for the entire years of of my life combined. God! given me a voice to preach the truth in cyberspace. It could end at any time if it be God's will, but you have no idea who is listening and but There are so many suffering people today. You can see it on their faces. They need answers, but all they're getting is garbage from government, pharmaceutical doctors who only want to make money . I heard Even when a wicked person is trying to harm a righteous man, the righteous man is ready to fight

Go on from here Chronic Inflammatory Demyelinating Polyneuropathy


Posted by

I have Peripheral neuropathy throughout my body. I was prescribed Levaquin in 2001.

Posted by

Took Levaquin 1.75 years ago and had extreme onset of bilateral pain symptoms in both hips, locking up, giving out, popping etc. Prior to this I was running up/down stairs and just no problems; afterwards using a cane. MRIs confirmed acetabulum labral tears in both hips. Now headed toward 2 hip replacements.
Researchers need to look closely at Levaquin and destruction of cartilage in weight bearing joints (not just tendons). It seems there are MANY others who have had labral tears resulting from Levaquin. I did fill out an FDA Medwatch form during the weeks after taking the Levaquin but never heard anything from FDA. My primary care Doctor also concurred that Levaquin brought on symptoms.

Posted by

Have taken Cipro An Leviquen. most recent use of Leviquen caused weakness of both legs before I finished 10 days of prescribed medication , weakness of legs an unstable condition continued after medication finished. Doctor said yes Leviquen causes those symptom's, should go away after a while. Cipro use after major surgery caused me to have loss of memories for short term periods, dose was 1000mg twice a day.


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