Fluoroquinolone Antibiotics: Are You At Risk?


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antibioFluoroquinolone antibiotics, Cipro, Levaquin, Avelox, etc. are broad-spectrum antibiotics used to treat a variety of infections, from urinary tract infections to anthrax and everything in between.  The first quinolone created was Nalidixic Acid which was discovered by George Lesher in 1962.  (Nalidixic Acid was added to the OEHHA prop 65 list of carcinogens in 1998.) Cipro (ciprofloxacin) is a second generation fluoroquinolone patented in 1983 by Bayer, Levaquin (levofloxacin) is a third generation fluroquinolone  patented in 1987 by Ortho-McNeil-Janssen (a division of Johnson & Johnson), and Avelox (moxifloxacin) is a fourth generation fluoroquinolone patented in 1991 by Bayer.

Fluoroquinolone Antibiotics – Still on the Market

Of the 30 quinolones that have made it to market since the 1980s, all but 6 have either been removed from the US market or have severely restricted use.

The fluoroquinolone antibiotics that are still on the market are some of the most commonly prescribed antibiotics. Per the FDA, “Approximately 23.1 million unique patients received a dispensed prescription for an oral fluoroquinolone product from outpatient retail pharmacies during 2011,” and “Within the hospital setting, there were approximately 3.8 million unique patients billed for an injectable fluoroquinolone product during 2011.”

When used properly, such as in cases of life-threatening hospital acquired pneumonia, fluroquinolone antibiotics can save lives.

Fluoroquinolone Antibiotic Side-Effects and Adverse Reactions

When used improperly, fluoroquinolone antibiotics can needlessly cause devastating side-effects.  Devastating side-effects can also occur when fluoroquinolone antibiotics are used properly, but the devastation can be justified by weighing it against the alternative – death.  In 2001, Dr. Jay S. Cohen published an article on the severe and often disabling reactions some people sustained  as a result of taking a fluoroquinolone antibiotic.  Dr. Cohen says,

It is difficult to describe the severity of these reactions. They are devastating. Many of the people in my study were healthy before their reactions. Some were high intensity athletes. Suddenly they were disabled, in terrible pain, unable to work, walk, or sleep

Dr. Cohen’s study of 45 subjects suffering from Fluoroquinolone Toxicity Syndrome, a name that I’m pushing for, (without an official name, it is difficult get the word out) showed that they had the following symptoms:

  • Peripheral Nervous System: Tingling, numbness, prickling, burning pain, pins/needles sensation, electrical or shooting pain, skin crawling, sensation, hyperesthesia, hypoesthesia, allodynia (sensitivity to touch) numbness, weakness, twitching, tremors, spasms.
  • Central Nervous System: Dizziness, malaise, weakness, impaired coordination, nightmares, insomnia, headaches, agitation, anxiety, panic attacks, disorientation, impaired concentration or memory, confusion, depersonalization, hallucinations, psychoses.
  • Musculoskeletal: Muscle pain, weakness, soreness, joint swelling, pain, tendon pain, ruptures.
  • Special Senses: Diminished or altered visual, olfactory, auditory functioning, tinnitus (ringing in the ears).
  • Cardiovascular: Tachycardia, shortness of breath, hypertension, palpitations, chest pain.
  • Skin: Rash, swellinghair loss, sweating, intolerance to heat and\or cold.
  • Gastrointestinal: Nausea, vomiting, diarrhea, abdominal pain.

When a fluoroquinolone antibiotic triggers a toxic reaction in a person, multiple symptoms are often experienced.

Fluoroquinolone Antibiotic Damage – Technical Aspects

Fluoroquinolones are eukaryotic DNA gyrase and topoisomerase inhibitors very similar to many antineoplastic agents (source).  What this means in plain English is that these drugs work the same way as chemotherapeutic drugs; they disrupt DNA and lead to destruction of cells.  A recent (2013) study conducted by a team of scientists at the Wyss Institute for Biologically Inspired Engineering at Harvard University Studies showed that Ciprofloxacin, along with a couple of other non-fluoroquinolone antibiotics, causes oxidative stress and mitochondrial malfunction. A 2011 study published in the Journal of Young Pharmacists found that, “There is significant and gradual elevation of lipid peroxide levels in patients on ciprofloxacin and levofloxacin.”  They also found that “There was substantial depletion in both SOD (superoxide dismutase, “a free radical scavenging enzyme”) and glutathione levels” and that “On the 5th day of treatment, plasma antioxidant status decreased by 77.6%, 50.5% (and) 7.56% for ciprofloxacin, levofloxacin and gatifloxacin respectively.” The study also notes that administration of fluoroquinolones leads to a marked increase in the formation of Reactive Oxygen Species (ROS) and that “reactive free radicals overwhelms the antioxidant defence, lipid peroxidation of the cell membrane occurs. This causes disturbances in cell integrity leading to cell damage/death.”

How Many People are at Risk?

The exact rate of adverse reactions to fluoroquinolones is difficult to determine.  Studies of adverse reactions to fluoroquinolones have noted that, “During clinical trials, the overall frequencies of adverse effects associated with (fluoroquinolones) to vary between 4.4 and 20%.”  Just the fact that the spread is so large, a 15.6% spread in frequency of adverse reactions is a HUGE difference, it implies that the actual occurrence of adverse reactions is difficult to establish or unknown.

With the FDA figures above noting that 26.9 million unique patients were given fluoroquinolones in 2011, if you just take the conservative adverse reaction figure of 4.4%, you’ll get a horrifying number of people with adverse reactions in 2011 alone – 1,183,600 people.  20% of 26.9 million is 5,380,000 people adversely effected.  That is scary.  Those numbers are truly frightening given the severity of the adverse effects described above.

Fluoroquinolone Toxicity Syndrome

I see fluoroquinolone toxicity everywhere, and even I think that those numbers are high for severe, disabling reactions like mine where multiple symptoms develop simultaneously.  Not everyone who has an adverse reaction to a fluoroquinolone has a reaction like mine, or even develops Fluoroquinolone Toxicity Syndrome. Many people have milder reactions.  Milder symptoms include any one of the symptoms listed above as well as  diarrhea, vomiting, mild tendinitis, decreased energy, painless muscle twitches, memory loss, urgency of urination, or any number of reactions that the body may have to a massive depletion of antioxidants and increases in lipid peroxide levels and reactive oxygen species production.

Even though severe adverse reactions to fluoroquinolones antibiotics can be painful and disabling for years, many (possibly most, but certainly not all) people recover from Fluoroquinolone Toxicity Syndrome with time.  I anticipate that I will be fully recovered 2 years after my reaction started. Sadly, there are some people who don’t recover.  They suffer from chronic pain, disability, impaired cognitive abilities, etc. permanently.

It is absurd, to say the least, that an acute problem, an infection, that can easily be taken care of with administration of an antibiotic that is not a fluoroquinolone, is converted into a chronic problem, a  syndrome that can disable a person for years, by a prescription ANTIBIOTIC, used as prescribed. In my case, a urinary tract infection that could have likely been taken care of with macrobid or even cranberry juice and d-mannos, was treated with Cipro which left me unable to do many physical and mental tasks that I had previously been able to do with ease. It’s a crazy, absurd situation.  It’s absurd and it’s wrong.

Some Antibiotics are More Dangerous than Others

The bottom line is that these popularly prescribed antibiotics are dangerous drugs that have caused thousands of people to suffer with a myriad of maladies. Undeniably, they have their place, in treating life-threatening infections.  Unfortunately, they are not being reserved for use in life-threatening situations and people are being hurt after taking them for simple sinus, urinary tract, bronchial and prostate infections. A strict and rigorous protocol needs to be established to limit the damage that they cause; because it’s not right to maim and disable people to treat their sinus infections.

Sources are highlighted throughout the article.


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More From 'Awareness'

CE provides a space for free thinkers to explore and discuss new, alternative information and ideas. The goal? Question everything, think differently, spread love and live a joy filled life.

  1. Fantastic article Lisa. I too was devastated by Levaquin 6 years ago; I am still unable to take care of myself. I lost everything and now live with my sister. It took me several years to figure out what had happened to me. The big problem with these drugs is that the vast majority of victims to not feel the damage they are doing until quite some time has passed so they do not suspect an antibiotic they took a while back when their tendons rupture spontaneously or they develop cartilage lesions or their heart starts fluttering or their lungs fill with fluids or their skin breaks out in a horrible rash or the become psychotic or they get neuropathy or they can no longer think clearly and on and on. Victims usually suffer a syndrome with many or even all of the “symptoms” and many others not listed here. These chemicals damage people from head to toe but the drug reps have the doctors fooled into believing these drugs are safe and that people claiming they were harmed by them are freeloaders so not only do doctors not believe us, they mock us smugly and treat us like crap. We are victims of a heinous crime; the execs in Big Pharma know exactly what they are doing. They are criminals of the highest order who should be behind bars for the rest of their lives. Please, unless you’ve been exposed to anthrax do not take Levaquin, Cipro, Avelox or any of the other fluoroquinones coming out. I’d take my chances with anthrax

    Reply
    • If you believe you may have been harmed by one of these drugs go the the Fluoroquinolone Toxicity Group in Facebook and the friendly folks there will try to answer your questions.

      https://www.facebook.com/groups/46690244194/

      Reply
      • The adverse reaction I experienced from Cipro (and Amoxicillin before that) translated in being classified as psychotic without an eventual correction. I was given Cipro while hospitalised and not receiving the usual Xanax dose I was taking then. Both drugs interact negatively in the GABA brain receptor. actually, being in Xanax withdrawal is what caused the “storm”. I ended up in a psych. Ward for 9 days while getting some antipsychotic medication to boot. My protests were interpreted as “proof” of mental illness. My health records still record me prone to psychosis because I cannot afford legal help. There is a lot more to this, but the picture is about this anyway. I have mostly “let it go” and retained a healthy enough dislike of the mental health world.

        Reply
      • Thank you! Anyone who reads this, please check out the facebook group. You are not alone.

  2. Cipro and Levaquin are quickly becoming a real threat to our society. The numbers of victims are growing. Thank you Lisa for covering this topic so well.

    Reply
  3. Ginny

    I was damaged by Levaquin, almost 5 years ago. Lost my career of over 50 years, due to muscle loss, brain fog, heart damage, 24/7 pain, all results of CNS, PNS, damage. Still suffering, there is no treatment or cure for this damage.

    Reply
    • Thank you for sharing, Ginny! You have my sympathy, empathy, thoughts and prayers. Thank you for pointing out that there is no treatment or cure. It is something that people need to know. Please have hope. Even though there is no cure, there is always hope, and sometimes there is healing.

  4. my name is james. cipro and levaquin has made my life a living hell. been to so many doctors and then to be told that they can not find what is wrong is insane. would never have known but bought a computer and now I know. I will always believe these doctors know what it is, but they are milking the money. I go to no doctors anymore and have helped myself more with supplements and herbs. I eat no meat, bread or sugar and that helps greatly. if anyone wants to storm big pharma, I am in.

    Reply
    • Thank you, James! I’m glad that you have found a diet that helps. Let’s storm big pharma! This isn’t okay.

  5. Michelle Banks

    I took Levaquin in April, 2013. I began having horrible side effects after the first dose. I was an active, healthy wife, mother and registered nurse. I have lost my job, my income and my independence. I have severe pain in my legs, tendon pain all over my body, and just recently had to have surgery on a tendon in my hand. Please don’t take these antibiotics unless it is a life and death situation. I had a very mild case of bronchitis, and now my health is destroyed.

    Reply
    • Michelle, thank you for sharing your story! I’m so, so sorry for your pain and loss. I hope that you find relief and healing with time. I know that it’s trite, but hang in there.

  6. Just a balanced view from the other side… I have Cystic Fibrosis and have had regular courses of Cipro over many years combined with many, many other antibiotics, and they have kept me alive. Yes treating mild infections with strong antibiotics is bad practice, and living in the UK I cannot comment on practices elsewhere, but here my doctors check blood levels to ensure the doses I take do not exceed safe concentration levels in the body which leads to (I’m assuming) the problems faced by many here.

    We should not blanket all antibiotics as a menace to our health when many lives have been saved using them as well. Without chronic infection there are many alternative treatments, however in my situation with severe pseudomonas, staph and mrsa cultures in my lungs, these drugs are keeping me alive. And just so you know, I do research the hell out of finding other natural therapeutic treatments and am trying to incorporate them as I learn.

    Reply
    • Thank you very much for your comment! Certainly, I am thankful that these drugs have kept you alive! That’s wonderful! When used appropriately, they can save lives. I don’t think that anyone is arguing that they can’t. But they are given out for infections in otherwise healthy people to treat infections that could be treated with other, more benign, antibiotics. I don’t think that they should be banned. But they should be a drug of last resort, not a first line of defense.

      The last thing I want to do is to “blanket all antibiotics as a menace to our health.” While they do have their problems as a general class of drugs, antibiotics generally have done a massive amount of good. FLUOROQUINOLONES, Cipro, Levaquin, Avelox, and a few others, are not the same as other antibiotics, and what I want to do is encourage people to realize the dangers of this particular class of antibiotics and to request other, more benign, antibiotics whenever possible. Yay antibiotics – except Cipro, Levaquin and Avelox! Fluoroquinolones, and only fluoroquinolones, can cause a disabling syndrome that can last for years, or can even be permanent.

      This is a quote from a friend of mine who told his story on the Fluoroquinolone Wall of Pain on Facebook, “From researching on respected sites such as PubMed, we found that Cipro is a member of a class of antibiotics called fluoroquinolones (or “quinolones” or “FQs”); Cipro and Levaquin are two of the most popular. If you google them, you can immediately see how dangerous they are. Of 30 quinolones that have made it to market since the 1980s, 25 have either been removed from the US market or have severely restricted use (http://en.wikipedia.org/wiki/Quinolone#Generations); that means 83% of these FQs have been banned, restricted, or denied approval by the FDA. By comparison, the good old penicillin antibiotic class has 16 members… not a single one has been withdrawn in over 50 years of use.”

      Thanks again for reading and for your comment and I wish you good health!

      Reply
  7. few months ago I suspected a bladder infection and after confirmation my wife’s doctor said: “Never Mind , I’ll fix you up.” 5 pills of 750mg of tavaloxx, 4 days later I couldn’t walk anymore. Left achilles tendon on fire and right foot swollen like a monstrous gout, terrible itch on skin lower legs. After 3 months I can walk again but feet and ankles feel inflamed and itch, I take magnesium tissue salts and fortunately I make an excellent biological red wine that may not be curative but is a great help. The inflammation must be the effect of the damage the quinolone molecule has caused, as yet I have not found a remedy to combat the inflammation. Yours, Nick.

    Reply
    • Thank you for sharing your story, Nick, and I’m so sorry for your pain! Not being able to walk for 3 months is a heck of a price to pay for a bladder infection, huh? I can empathize. I took Cipro for a urinary tract infection and had all sorts of nervous system issues – central, peripheral and autonomic nervous systems – for the following 21 (and counting) months. I also had inflamed tendons throughout my body. Sadly, there doesn’t seem to be a single cure that helps everyone. However, there are people who are able to recover and heal through a variety of different methods. There are some stories of hope and healing from Fluoroquinolone Toxicity on http://www.floxiehope.com. There are also support groups on facebook with lots of friendly folks who can help you through this, if you need and want help. Here are some links for the facebook groups – https://www.facebook.com/groups/46690244194/ and https://www.facebook.com/groups/261231253984443/ Good luck and please let me know if you need anything! You can contact me through the “contact me” link on floxiehope.com.

      Reply
  8. Let us not forget that if you already have CDiff in your gut, it allows it to run rampant, as it did in the case of my elderly mother. She died because she contracted CDiff from the hospital where she was given prophylactic (quinolone) antibiotics before a routine procedure to remove a trapped gallstone. A week later she ended up with sepsis from the CDiff and her bowel ruptured and her heart stopped – until that day, I never realised how devastating CDiff could be – neither did half of the professionals that treated her – they didn’t have a clue!

    Reply
    • I am so, so, so sorry for your loss, ghwindyweather! Maybe someday people will realize the harm in waging a war against the good bacteria in our gut. Unfortunately, the realization will not bring back your Mom. Thank you for sharing your story. My condolences for your loss.

  9. I told you a few weeks ago that I had also been hammered by an equilone antibiotic. I live in South Africa and the poison that is brainwashed into medical doctors brains(?) is called Tavaloxx, made by a florishing firm, Cipla, that has just been acquired by a company from India. When I got hold of one of these Cipla people in order to give them a piece of my mind, the stupid fellow asked me right away whether my achilles tendon had been ruptured. For me this is sufficient proof that these pharmaceutical chappies know perfectly well the deleterious effects their pills may have on our bodies. However I have lived and learned for a good 80 years and to get buggered up the first time in my life I went to a GP annoyed me no end and I decided to learn some more to get myself right again. I have now been treating myself with tissue salts, a discovery by dr.Schussler about 150 years ago, I think. Go into the net to find out what are tissue salts, I buy them here in healthshops and pharmacies. Check out the modern names for these products as, for exemple, Natrium Muriaticum is today potassium chloride, an important one for us floxies. Magnesium phosphate you must take, in fact, all the 12 tissue salts can be taken as there is no way they can harm us. I also took some Epsom salts, Magnesium sulphate, which is much more concentrated than tissue salts. Take it easy on that stuff and remain in the vicinity ok humankind’s greatest invention, the flush toilet. As we’re all different, the stuff that worked for me might not have the same effect on you but it canna harm you. I’m almost back to normal, my toenails that had stopped growing for 5 months show spring time growth and a 5day fast improved matters also. More I cannot tell you except to express my astonishment that none of you folks have not attacked judicially the perpetrators of these pharmaceutical misdemeanours. None of your lawyers are interested? Nick Dekker.

    Reply
    • Hello again, Nicholas! Thank you for your comment! I appreciate the mention of tissue salts. I have been using epsom salts to soak in since I got floxed. I haven’t tried Natrium Muriatacium / Postassium Chloride but I certainly will. Do you drink the tissue salts or do you just soak in them? I am so pleased that you are feeling better! I too have found healing. As you mentioned, everyone’s healing path is different and, sadly, some people don’t heal.

      The achilles tendon problems are acknowledged by the pharmaceutical companies and the regulatory agencies in our countries. What they fail to mention is that your achilles isn’t the only tendon that can be adversely effected. EVERY tendon in your body can be destroyed and you can rupture a tendon getting out of bed because of these drugs. They also damage every nerve in the body and wreck havoc on the central, peripheral and autonomic nervous systems.

      Some people have successfully sued the pharmaceutical companies that have hurt them. Unfortunately, the warning labels on the drugs serve the purpose of protecting the pharmaceutical companies from liability more than serving to protect people. Very few lawyers are willing to take the cases of “Floxies.” The damage that these drugs do is so complex that it is difficult to prove that they are the culprit. Everyone prefers to believe that the rise in “mysterious diseases” and pharmaceutical poisons aren’t related. It’s absurd and it’s wrong.

      • Linda

        Hi Lisa,
        Thank you again for your help yesterday. I am new to all of these websites and searching for solutions. I have been using epsom salts but now have a mysterious rash on my legs along with the neurological and musculoskeletal symptoms. The dermatologist said I need to use cortisone and take antibiotics which I am not doing. I have been afraid to use the epsom salts since the rash.
        Have you experienced rashes from this fluoroquinolone poisoning? Should I continue with epsom salts during a rash? Is it okay if the epsom salt bath is hot when there is inflammation of the skin?

        Reply
        • Shawn

          Linda,
          Not sure you’re still on here, but I too have FQ toxicity (5 months and counting). And I, too, have folliculitis. Mine is along the back of my left leg (thigh and calf). Interestingly, this is the main location of my significant nerve issues (tingling, buzzing, etc.). No folliculitis on my right leg (yet) and none on the front of my left leg either. Anything that worked for you? I have been using a benzoyl peroxide wash that has calmed it but never knocked it out. At this moment, it is coming back strong. Freaks me out…

          Reply
          • Linda

            The dermatologist classified the rash as folliculitis but I think she was probably wrong, just as yours is. I do think the rash is related to the nerve issues. Skin is very emotional. All the worrying we have been doing about FQ toxicity and what is happening to us is probably one of the causes. I have calmed down now and the rash is now practically gone, very faint and I have not done much. Some mercola.com friends advised I try the ayruvedic pitta pacifying diet, since rashes are inflammation and the pitta type of person is prone to this. I have been doing this and maybe this too has helped.

            I did have one scary spinal episode where there was tremendous pain and I could hardly walk. After this I went to one of the doctors who had a good recommendation on the floxie’s list, Dr. Loren Fishman in NYC. When I told him I took Levaquin 5 years ago he dismissed the possibility that it could be from FQ toxicity. After testing me with needles hooked up to his computer, he said he thought I had a pinched nerve and spinal stenosis, but sent me for an MRI to make sure. He was right. Spinal stenosis is a narrowing of the lumbar lower portion of the spine and this causes pinching of nerves. There is also some disc damage. Whether or not this is from the fluoroquinolone or just part of aging, or caused by years of overdoing it at the gym and ballroom dancing fast salsa “on2″ with partners more than half my age I do not know. I have learned that the best thing for spinal stenosis is keeping the back straight, that means no yoga forward bends with an arched back, and no yoga backwards bends with back extension. High impact exercise like I have been doing is out. But I still can dance, continue dancing and am going for PT at Dr. Fishman’s office.

            Reply
        • Linda, certainly take this for what it’s worth (far less than the advice of a medical professional who has actually seen the rash), but you may want to try using coconut oil on the rash. It has antibacterial and antifungal qualities and it may be helpful.

          Steroids and antibiotics are the go-to drugs of too many doctors. When the antibiotic used is a fluoroquinolone, the combination of the antibiotic and the steroid can be disastrous. Personally, I avoid both antibiotics and steroids now. Your caution and wanting to wait for a culture is very smart! If it turns out that an antibiotic is necessary, all antibiotics that are not fluoroquinolones don’t have the long-term adverse effects of FQs and are generally safe. Aim for the mildest, most specific antibiotic possible.

          Reply
          • Linda

            Lisa I appreciate your thoughtful suggestions. In addition to the epsom salts and ACV baths, I am topically applying ACV to the rash and I waiting to see if this helps. If it does not work, I will try coconut oil. I already use coconut oil every day for cooking and brushing my teeth, oil pulling.

            Today my left calf is so tight it is hard to walk. Next Monday I am seeing one of the docs on the list you generously provided for the problems with my hip and leg, Dr. Loren Fishman. In addition to being an MD, he is a PT. It is so strange to suddenly go from being an extremely active person jumping rope and lifting weights to one who is hardly able to walk without discomfort. My friends at the gym are probably wondering where I am.

            Reply
        • I’m happy to help, Linda! If the epsom salts are giving you a rash, I’d say it’s best to stay away from them. As Ginny noted below, a rash from epsom salts has happened to others. There are other ways to get magnesium into your system. I take a 250 mg. supplement of chelated magnesium daily. As for the rash, both my rashes and hives went away with time. Antihistamines helped a bit and they don’t seem to hurt people who are suffering from FQ toxicity (but don’t take benadryl too often, long term use has been connected with memory loss). Acupuncture, and the herbs that my acupuncturist gave me, also helped me. I would stay away from both the cortisone and the antibiotics – but that’s just me.

          Reply
          • Linda

            I am pretty sure the rash is not from the epsom salts but only from the FQ toxicity. I was not sure if epsom salts would worsen it. I read about adding apple cider vinegar to the epsom salt bath for making rashes go away and will give it a try. Anyone used this combination? Has anyone tried oil of oregano topically on the rashes?

            The outbreak is on the backs of my thighs. The dermatologist said it was folliculitis which can be bacterial or fungal, probably a misdiagnosis. I am glad she sent a culture to the lab for analysis. It is scary that she gave me prescriptions for steroids and antibiotics and told me to start on both without even being sure exactly what the rash is.

            Reply
        • Ginny

          Linda, I am a victim of Fluoroquinolone Toxicity as well, and yes I was doing Epsom salts for the first year or so, and started with a rash. I stopped for a year then, had DNA testing done with a company called 23andme, and the results stated never to use Epsom Salts, because I a gene Mutations, which I likely got from my toxicity from Levaquin…..I found the facebook sites The Fluoroquinolone Toxicity Group, and Fluoroquinolone Toxicity 24/7 Live Chat site, back 4 years ago. huge support and love, only because of that am I still alive, I am a 5 year survivior TODAY, Oct 23, 2008 poisoned by Levaquin, instantly…….

          Reply
          • Thank you for your response, Ginny! I hope that your next 5 years are better than your last!

            Reply
      • Lisa, I use tissue salts in tablet form. I think you’re not well asqainted with these salts, you should try to get hold of Margaret Roberts’ book ‘Tissue Salts for Healthy Living; Spearhead, division of David Philip Publishers. It is the best book on the subject. Epsom salts: I mix a teaspoon full of salt in a glass of water and drink it through the day, twice a week and then nothing for the next week. Yours, Nick. To reply to you is troublesome I’m sorry to say

        Reply
        • Thank you, Nick! I will look into both of your suggestions. Please don’t be troubled! Until there is an official protocol for treating Fluoroquinolone Toxicity, we each have to find our own way – mainly through listening to advice from others with helpful tips. My healing path has not included tissue salts thus far, but I will certainly consider them in the future – while close to a flush toilet, of course.

  10. Lisa, thank you for the article, I am grateful for the impact you are making in spreading awareness and sharing a message of hope and inspriation. I wonder if you would be interested in reading my blog at http://www.survivingcipro.com and then sharing a conversation with me? Blessings, Nikki

    Reply
    • Hi Nikki! Thank you for all that you’ve done with SurvivingCipro as well! I would love to converse with you! Either through facebook or via email work for me. If you want to email me through the “contact me” link on floxiehope.com, I’ll get your email address through there and get back to you. :)

  11. Diana

    I was prescribed Ciprofalxacin HCL 500mg x2 per day for 10 days by the ER who diagnosed me with a UTI. I was also given a dose through my IV while I was in the ER. Within a day or 2, my infection definitely felt better but this is where my life began to change. By day 3, I began having severe headaches, insomnia, nausea, constipation, bloating, burning pain throughout my body, brain zapps, numbness, bone pain, major anxiety and panic attacks. I stopped taking the Cipro by day 6 due to severe migraines. Went back to ER, the doctors dismissed the fact that I believed it was from Cipro. Went back to ER 2 days after that because I felt like my head was going to explode. Doctors feel like I am under too much “stress”. Go figure! I feel like I am going crazy. My life is not the same.

    Reply
  12. Gilbert

    November 2014
    I continue to experience the following side effects since taking the Drug Cipro in October last year (2013)
    Peripheral Nervous System: (Polyneuropathy) numbness in arms and heel pads of both feet, prickling, burning pain in arms at night, pins/needles sensation in both arms and fingers, electrical or shooting pain, skin crawling,
    Central Nervous System: Dizziness,
    Musculoskeletal: Muscle pain (calf muscles), weakness, tendon pain,tendon ruptures in both Achilles tendons (reducing walking to a very slow and painful shuffle, and extreme pain in walking up inclines) .
    Special Senses: Increased tinnitus (ringing in the ears).
    Skin: Intolerance to heat and\or cold, and skin painful to the touch around the tendons affected, calf muscles and shins
    i have experienced some relief of late however in the pain and walking discomfort from the Ruptured Achilles tendons, due to nightly massaging of both feet and ankles and calf muscles by my dear wife Maggie, using a Magnesium spray and Cold Pressed Peanut oil
    First thing in the morning, I spray both Achilles tendons with Yunnan Baiyao spray ( a bit from each can) and this gives some relief until the mid to late afternoon.
    The polyneuropathy however seems to evade relief and is pretty constant throughout the day (Pins and Needles and Pain in forearms and being experienced mainly at night which disturbs sleeping quite effectively)
    I have also tried (with some success) several Rife programs, mainly those for Circulation, Lymph, Contusion, Arthritis, Detox and Tendinitis.
    My sympathy goes out to all fellow sufferers, many of who are in a far worse position than I am in.
    To those who may yet have this class of drug prescribed..read the warnings carefully, take note that there a large number of people out there who suffer these side effects
    Your Doctor should be aware, especially when they wish to try this course of medication to fix bronchitis, bladder issues (especially in women) sinus and ear infections
    My Pharmacist explained to me how toxic the flouroquinolones are and says he really hates to dispense it

    Reply
    • Thank you for sharing your story, Gilbert! I’m so sorry for what you are going through! I’m glad that you have found some things that help you, and that you have received acknowledgement from your pharmacist.

      If you are interested in sharing your story on http://www.fqwallofpain.com or http://www.floxiehope.com, please let me know. You can contact me through either of those sites.

      Regards,
      Lisa

      Reply
  13. Deb

    Thank you for this article. I was diagnosed with interstitial cystitis in 2004. Prior to this, in 2001 I had a severe UTI that was treated with Cipro. I was incredibly ill with extreme vomiting, feeling dizzy, faint, weak. I happened to be on a business trip when this happened. I needed a wheel chair at the airport. This went on for a few days after I began the Cipro. However, at the time I didn’t even cross my mind that the antibiotic may be responsible. I assumed the UTI was causing this because it had been missed and by the time it hit me it was so severe. I was also given another dose of Cipro in late 2004 during a cystoscopy w/hydrodistension & biopsy to test my IC further. I was then given Macrobid 1x per week for a 6 week period of bladder instillation to prevent infection. I had these rounds of 6 week bladder instillations three times in 2005. In November 2007 I was given Levaquin to treat another UTI. Now, after nearly 15 yrs. my IC has worsened, I am disabled emotionally and physically, I’ve lost everything I worked for and my IC has developed many friends such as chronic Pelvic Floor Muscular Dysfunction, Irritable Bowel Syndrome, Vulvodynia, Chronic constipation, depression, Generalized Anxiety Disorder and in the last 2 yrs. Panic Disorder w/agoraphobia, Low Thyroid, Vitamin D Deficiency, Bursititis in my right hand, hip and ankle. I began to question the cipro and levaquin finally now since I’ve been unable to get answers for what is causing my panic disorder and especially the Bursitis which I feel doctors just decided on calling it since my tests for rheumatoid factor, SED rate, etc… came back negative. I’m sorry for the long winded history. My specific question is can the effects of these medications happen years later or is it just while you are on them? I doubt there is anything I can do about it now. What is done is done. I just still want to know if it’s a possibility. Thank you again for the article and the replies of others who share their experiences is very helpful.

    Best,
    Deb

    Reply
  14. kim

    Thank you so much for this – however, Please remove your reference to Macrobid as a safe alternative,.
    Macrobid (Nitrofurantoin), years of it as a treatment for UTI’s and as a prophylactic has left me severely disabled with every symptom mentioned here. The symptoms that are the worst are the neuropathy , anxiety, migraines, sweating and breathing issues/lung damage. “Macrobid Lung” or “Nitrofurantoin Lung” kills people, mostly women. Pubmed has plenty of links for that. The neurotoxicity is a lesser known SE. This has destroyed my life.

    Reply
    • Hi Kim,

      You are absolutely correct and I apologize for not knowing about the dangers of macrobid/nitrofurantoin when I wrote this post. Macrobid/nitrofurantoin also has devastating adverse effects that can be long-lasting. I’m so sorry for what it has done to you! I hope that you recover your health and your life. There are stories of healing from fluoroquinolones on http://www.floxiehope.com. Several of the stories are from people who took both a fluoroquinolone and macrobid – myself included. I have made a full recovery and I hope for the same for you!

      Best regards,
      Lisa

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