are all my symptoms side effects of ciprofloxacin? any experience?
Posted , 21 users are following.
My doctor said I had a kidney infection so prescribed ciprofloxacin after taking first dose I felt very sick and after five doses woke with terrible pain behind left eye and over forehead, went back to docs who said its sinusitis and I have developed a terrible chesty cough, now tendonitis in right heel.
Is all this because of these tablets? Will I get better? How long will it take? I have two small children. Thanks you for any replies
1 like, 67 replies
emma_77009
Posted
My partner works a lot so I'm not gonna get much chance to rest or wallow in self pity for long with two young children. I'm not quite sure my partner actually believes all this can come from antibiotics.
You've given me hope knowing things will improve, thanks for the help.
Tarun
Posted
To me it seems as though the GP is taking the tendonitis a bit too lightly. As a pharmacist we have always been told to counsel a patient to stop taking a quinolone antibiotic (such as ciprofloxacin) if symptoms of tendonitis develop because of the risk of tendon damage. Agree with the above comment to avoid anti-inflammatories for the time being.
Tarun (hospital pharmacist)
billa58896
Posted
I've approached pharmacist s and excuse me for saying this but don't seem to know a great deal about interactions if the drug. I was even told to take ibroprofen by one gp!!.
If I tailor my diet to the repair of these particular cells un your opinion do you believe this will help?
Chris
billa58896
Posted
Any advice (from a professional) wiuld be greatly appreciated.
billa58896
Posted
That things will get better with time.
Rest/ice will not necessarily work.
Tarun
Posted
As for the previous post, ciprofloxacin and other quinolones (and indeed antibiotics in general) work because they target bacterial cells rather than human cells. Antibiotics are designed to target differences between human cells and bacterial cells otherwise they would be useless drugs because they would cause too much damage to humans. Ciprofloxacin targets an enzyme that is ONLY present in bacteria. I'm not entirely sure what effects if any it has on human cells - I would leave this to researchers to be honest ! When you start doing trials and studies at this level it becomes near impossible to prove a specific effect of a drug on the body based on lab tests.
madge07350 Tarun
Posted
miriam65408 madge07350
Posted
Hi Tarun, if you're still about Madge is absolutely correct. It was discovered as long ago as 1996 that Cipro actually affected mitochondrial DNA (but not cell nucleus DNA), but it's not exactly been top agenda worls-wide news. One could even imagine that this information is deliberatly being kept quiet! Signs of mitochondrial damage are definitely something you should have been trained to look out for. I can't give the complete address of the paper as it will be taken down to be moderated, but searching for this should find it: “Delayed Cytotoxicity and Cleavage of Mitochondrial DNA in Ciprofloxacin-Treated Mammalian Cells” published in Molecular Pharmacology in 1996. Lawrence et al. Hope this helps others in their research too.
miriam65408 Tarun
Posted
Hi Tarun, if you're still about Madge is absolutely correct. It was discovered as long ago as 1996 that Cipro actually affected mitochondrial DNA (but not cell nucleus DNA), but it's not exactly been top agenda worls-wide news. One could even imagine that this information is deliberatly being kept quiet! Signs of mitochondrial damage are definitely something you should have been trained to look out for. I can't give the complete address of the paper as it will be taken down to be moderated, but searching for this should find it: “Delayed Cytotoxicity and Cleavage of Mitochondrial DNA in Ciprofloxacin-Treated Mammalian Cells” published in Molecular Pharmacology in 1996. Lawrence et al. Hope this helps others in their research too.
Ploddingon
Posted
My story is written on another discussion here called 'Ciprofloxacin Poisoning?' but I would just like to add, that I was first affected by Levofloxacin (same group of Fluoroquinolone antibiotics as Cipro) 9 months ago, and I literally couldn't walk for nearly 5 months and was in severe pain. The good news is that now I have improved hugely. I still have pain in all the affected tendons and can't walk for too long but things are so much better.
I agree all that Chris above, has said and wouldn't bother doing the rounds of many medical specialisms. I am not a doctor but from my research on Fluoroquinolones, which has been quite extensive, I don't believe there is any quick fix and you do have to take care for a few months yet, that you don't put too much strain on your tendons (especially the large ones) because of the risk of rupture. As Chris says, Collagen is destroyed and doesn't actually regrow exactly the same as before the toxic effect - because the DNA strands are damaged.
The reason why this particular group of antibiotics causes so many problems is that it penetrates more deeply than others and doesn't only attack bacterial cells, contrary to what Tarun says, I'm afraid.
I would also strongly urge you to get your GP to mark your notes in bold, that you must never be given another Fluoroquinolone!
I wish you a speedy recovery........everyone else too.......
Very warm wishes
Plodding on
Ploddingon
Posted
There is also a very comprehensive list of all the Fluoroquinolones and their brand names on the Quinolone Vigilance Foundation site.
Plodding on
billa58896
Posted
As all my blood tests have come back normal uts difficult for me to prove anything anyway, and believe me if u pursue this its likely that you'll be treated like a hypochondriac. Better just get on with and hope that you'll body will recover through a nutritious diet and exercise.
Chris
Ploddingon
Posted
Although my blood tests didn't show anything unusual, the Ultrasound on my Achilles tendons and feet did show damage and I was asked if I was a regular serious walker or went running........I have never done either and so the damage was attributed to the Quinolone.
Plodding on
billa58896
Posted
Also what are your symptoms? I just ache around my ankle achilles area, it doesn't stop me from walking/swimming/cycling but it is constantly there.. also they ache by thw end of the day. Therws no stiffness, theyre not aesnsitve to touch or painful just achey. Is that similiar to you.
I won't be pursuing this any further through rheumatologist though as I don't want people thinking I'm juat making this up and by all accounts I just want to get on with life..
Ploddingon
Posted
My symptoms with the tendons, sound like yours are at the moment - lots of aching, especially by the evening. At first the pain was horrendous and I couldn't even lift my feet off the floor; I could only shuffle (luckily I have wooden floors). Both Achilles and all the tendons round my ankles plus under and across my feet were affected and I could only lie there, with my legs wrapped in wheat bags that were heated regularly in the microwave and I took (still do) liquid morphing for the pain.
I saw a musculoskeletal specialist! who sent me to a physiotherapist. He gave me exercises to do with Resistance Bands but these made my knees hurt and the pain afterwards was really bad. He did say it would take months of physio but in the end, after discussing it with my GP, I stopped going, because the Physio was setting me completely unrealistic goals. My GP felt, as I did; that I knew my own body and I could do gentle stretches and heel lifts but slowly. I have been recovering myself really, without doing anything specific. I have been told that Physios who have had no experience of this unique type of tendon damage, should be avoided, as they don't understand that it is unlike a repetitive strain or sport's injury, as the breakdown of the collagen is all over the tendon and that it's a case of gently trying to help the collagen repair faster than it breaks down. The action is like a cascade throughout the body and it's ongoing, as opposed to stopping once the drug has left the system - it never actually does.
Sorry, I've banged on a bit here.......I've heard swimming is good but I can't do that as I have other health issues that prevent me. I do believe that slowly slowly is the way, with much care.
Plodding on
james67815 Ploddingon
Posted
I was also put on Cipro for epididymits but is not . Four weeks of Cipro 1000mg aday now I feel so weak constant nausea and urge to go loo I'm 36 male suffer from anxiety / depression now worrying I have surfing more worse . Doc again today at 14.40
madge07350 james67815
Posted
You are probably suffering from Fluoroquinolone Toxicity. That amount of Cipro for so long could severely affect you for years to come. I would get off it as soon as possible . The anxiety and depression are well known side effects as are the physical symptoms you are experiencing. But you need to watch out for tendon pain as well as ruptures of the Achilles tendon can happen months later on this drug. And don'the let your doctor tell you that only happens to old people who take steroids. It happens to people your age as well.
miriam65408 james67815
Posted
Hi James, Just wondering how you got on with the doctor? They often don't believe Cipro has side effects (despite the lengthy list on the leaflet!). You've had a lot of Cipro and anxiety and depression are symptoms. Have you had any muscle/tendon aches and pains? Don't take Ibuprofen (or any other NSAID) or any steroids, as these can make everything worse.
james67815 miriam65408
Posted
I'm back Wed not taken anymore Cipro but still unwell waiting on blood test . And started on antidepressants again
miriam65408 james67815
Posted
The blood test will probably show nothing is wrong. Cipro damage doesn't seem to show up in any tests. Get your doctor to go through the information leaflet that was in the packet with the Cipro pills with you. Tell your doctor which of the listed side effects you are currently suffering from. He/she can't deny it was the Cipro if it's there on the list!
Have you tried to join the UK Fb group? If you have. check your message requests as you need to email. If you haven't, go to the moderator's post on this site at https://patient.info/forums/discuss/fluoroquinolone-toxicity-syndrome-427305
and look for the UK FB site and their website. I hope this helps - the website will have information to show your doctor, look on the Links page.