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Hey Lisa, Have you noticed the new study about increased death rates among middle-aged Americans by Drs Deaton and Case due to pain medicine and alcohol poisoning?
“Recent reports of illness and disability might provide some clues. More middle-aged whites report that their general health is not good; and, more report chronic pain — neck pain, face pain, joint pain, sciatica. More report mental distress or mental illness. More say they have trouble walking a quarter mile or climbing stairs. More say they have trouble shopping or socializing with friends. More say they can no longer work.”
You need money and insurance to be able to “report” and get the prescriptions, which might explain the race bias.
Lucy Sky
9 years ago
Does anyone know what the contra indications are of chamolile please?
Lucero Rojas
9 years ago
Hi everyone! Hope each of you are doing good. Just want to mentioned this here. I started seeing a doctor who has the same theory as Jason, that many Floxies got this way because they have Methylation issues and it could be key to some peoples recovery. Genes have alot to do with things like this. The way we detox, why he got sick when others never had a reaction with this drugs.
Lucy Sky
9 years ago
Sensitivity to noise, light , to smells, cramps, spasms of muscles esp the Achilles tendons, burning of legs. I hope that these people get put in prison. I have to see the out of hours drs in the morning to be checked over due to the chamolile drops given to me yesterday.
On a point of interest the camolile increased the burning and spasms. I wanted to know if anyone else had ever tried camolile and what their experience of it was.
I have just found out that garlic is contraindicated with warfarin!!!
What a night mare. Before being floxed I could eat anything.
Jason
9 years ago
Hi Lucy. These questions you asked last page about Adrenal Fatigue and Thyroid are pretty complex questions and issues, and all these things have once again many causes, please do not jump to any conclusions, proper testing is important before trying to discern the what and the why etc. Without testing, someone can have 15 or so symptoms of 15 or more different ailments, which all share many of the same symptoms, this is one reason why there is so much misdiagnosis out there everyday. You mentioned your Cortisol was only “slightly” elevated, it can fluctuate a lot as I mentioned before, and I am not sure how that was tested for you but let’s remember here the Hyperthyroidism, Insomnia, etc these things that you are struggling with are known causes of exhaustion yet again.
Having said all that, yes, IMO, Cipro “can” affect the Adrenals in many ways, there are numerous causes of AF, just plain old stress/anxiety is one of them, I know there are a lot of stressed out Floxies out there physically and otherwise, eventually this can take its toll on the Glands. There are other things that can happen here too related to Cipro (and others still that are not), Hormonal imbalances, Mineral/Electrolyte imbalances like Copper Toxicity which often shows up with AF (<=ME), Neural Transmitter imbalances, maybe more that's just off top of my head. Note also there are several "stages" of Adrenal Fatigue, and someone's symptoms vary depending on where they are at if they are going through it. What I eventually did was get a Hair Analysis test, this tests someone for Toxic Metals and many important Mineral/Electrolytes (the one I did was about 40 or so things tested. The other test I mentioned before is important too. I also had a Cortisol suppression test done but note this uses a fluoridated drug!
Does Cipro damage the Adrenals directly? I don't know, and I don't think anyone else does either as far as I know but I could be wrong on this, I don't recall seeing this anywhere however, and even if there is no info we have to remember no one knows the full extent of damage this drug does. Also note, I "don't think" AF itself is going to affect someone's Thyroid, I could be wrong on this too but really don't think so.
Treatment depends on the cause, what stage someone is in, etc again a good Naturopath will know these things, otherwise they wouldn't be that good IMO. If your Sodium is sky high and you take things to bring down your Copper, you can see how this won't be helpful, root causes! M.D.'s are the turkeys who treat symptoms, which is the WRONG way to treat patients! Without testing, if someone just starts taking supplements first off they might be wasting time and money since they may not have AF at all, 2nd they might make it worse by causing worse imbalances. I hope you see how important these 2 points are, and they apply to a whole lot of ailments, maybe all of them.
AF itself is actually just another symptom, not a root cause. First you can exhaustion for example as a first symptom noted, from there with testing someone might discover they AF, however they still need to know why, some of the causes are above but there are others still like too much stimulant use, essential Nutrition missing etc. In my case I am quite sure there were several causes, and this can get tricky; stress was eliminated long ago yet I still had AF, being stressed too long in "fight/flight" mode will drain your system, once your system is drained your body can start accumulating Copper as you may not be "using it" properly anymore, in my case I was at toxic levels which can then keep the Adrenals down as the Copper is then thought to be "unavailable", so I needed to bring this back into balance which I did (yes I treated myself to answer your other question). Here is the rub for me, the "root cause" was still not revealed until after all this, once my Adrenals started "functioning" properly again, now they are working TOO MUCH! I feel this through having "butterfly" feelings in my gut, which I am sure is excess adrenaline, and when it really gets excessive I can crash again. Here again there are several causes on why, it could be things are not yet fully balanced, an issue with the gland itself, others, or the most probable cause to me when I look back on my last 30 of almost 50 years of not feeling right, I have COMT/MAO Genetic SNP issues which basically means I often have excess Adrenaline and can get stressed out easily. I can tell you that now that they are working again, there have been several recent instances where Adrenaline went overboard and I crashed, and it was for something simple like a Tennis Match which is nothing stressful, you can see how important something like this is. I have not tested this last part yet to confirm this suspicion, but it makes the most sense.
This is not the best website but it is more basic than some of the others where things are more complicated, so its a good starting point.
As for the Thyroid questions, I replied to one of your messages 2 pages ago which I suspect you did not see. I will make another more detailed post for you about it soon.
Of course these are all my unlicensed opinions as usual.
Leslie
9 years ago
Hi everyone- I’m sure this has been discussed to death but I just got my 23 and me results and wondering what program I should put them through so that I can understand this information. BTW I am 7 months out. Starting improving at 5 months out. Still have a long way to go. Thanks in advance!
Agats
9 years ago
Hello
My name is Agata and I 36 years old. In year 2013 I had back surgery…..herniated disc. Since the anasthesia my problems began. Al my joint are afected. The main simptom is that ligaments strech so easy and the joint is than unstable. I am living with a lot of pain and disabilities. It looks like I have connective tissue disease but I dont. It all started after general anasthesia, and the anasthetic was Sevoflourane wich is highly fluorinated. Could this be a reason? What test to be done? It is 2.5 years from surgery and it is still progressing.
Sory for mistakes in language. I from Slovenia ..Europe.
Lucy Sky
9 years ago
Does anyone know if there is any fluoride in clexane, marcain and or chamomile. BTW Chamomile is not recommended for various reasons, it is not tested thoroughly etc, etc.
Does chamomile adversely affect the heart?
Agata
9 years ago
Hi lucy
I am sorry for you but I can’t give you any advice because I am new in this. My simptoms began in year 2013 but I just now realised that must be fluor. Soo I can’t give you any advice because I am looking for advice too. But I am asking you, did you get any offical conformation from doctor that is fluor causing you this. Any lab test? Here in Slovenia they have no clue abaut that, or I am just so unlucky and the doctors I see are not the right one.
Lucy Sky
9 years ago
Hi Agata
Nice to meet you.
Yes I have a medical report stating the cause is due to antibiotics. I have had cipro on a few occasions but it was only 19 months ago following the prescribing of three antibiotics at ONCE when I was struck down with an acute attack.
Chamomile made things worse . It is under researched and under tested. it is contraindicated in people on warfarin and with epilepsy etc, etc.No doubt people will say the same about drugs as well. Just because something is ‘natural’ does not mean it is safe.
Sorry but I am going through a very rough time at the moment.
Jason
9 years ago
Debs & Lisa. Is there a list somewhere of all the Quin & Fluoridated & other closely related drugs somewhere? And a large list of what “might” be safe, including bluddy anaesthesia options? Lisa did you make an article before compiling them?
I have to admit I am a little bit terrified of getting into an accident of some kind, and being brought to the Hospital for surgery unconscious or debilitated, and then being given Fluoridated anaesthesia & quin related drug, good God.
The website above has a pretty comprehensive list of “F” drugs, but what about the Quin and closely related ones, and any other ones we know interact badly like Steroids etc. TIA
Agata
9 years ago
Hi Lucy, Daniela, Jason
I am very confused abaut my condition. Because here in Slovenia we don’t fluorinate our water, I have healthy diet because my brother has a farm and I am eating healthy home vegetabel, meat and other stuff, grown withaut any cemicals, pesticides and I was healthy befor with the same diet I have now. It all started after surgery and still progressing. My only simptom is ligament laxity, or I woud call it ligament strech syndrome and hyperrefleksia. And if I am thinking right that fluor in my body should be getting out and the symptoms would slowly stoped..but they are progressing. Why? If I am not getting any fluor in my body by the water or other stuff. They tested me for genetic diseases of connective tissue, and autouimmune and inflamatory. What the hell is going on?
Lucy Sky
9 years ago
Hi Agata Have you been tested for lupus? Some drugs can give you lupus, for example phenytoin, the ppi’s statins, antibiotics, have your anti nuclear antibodies and ebv -for glandular fever been tested? Have you had a double stranded DNA test done?
Are your temperature and heart rate normal?
What meds if any are you or have you recently taken.
Lucy
Lucy Sky
9 years ago
Dear Lisa
You may want to modify this .I don’t mind.
Please google local anaesthetic drugs and adverse reactions. Note marcain, inexpensive local anaesthetic drug et most cardio toxic LA as stated previously.
You may also wish to google anaesthetic agents with fluorines.
Think about dry cleaning agents that contain solvents too.
Anaesthetic gases contain solvents. For example Trilene.
HALOTHANE – this causes liver damage. Then we have entonox which can cause seizures and peripheral neuropathy.
Scary so may not wish to look it up. Sorry gang.
Lucy.
Brian
9 years ago
Has anyone else experienced their bowel movements being a bit “off” in terms of its color? I don’t have any pain and I’m pretty regular but it’s a very light brown to almost yellow hue every time. This has been pretty consistent since I stopped taking Cipro. I told my doctor but he didn’t seem at all concerns. Ran a bunch of tests and all my blood work came back normal. Liver functioning very normally/kidneys fine/etc. Is this sinply due to the bad bacteria being killed off? Or perhaps stress/anxiety?
Agata
9 years ago
Hi Lucy
I have been tested for lupus, They did ANA test, abaut glandular fever as far as I was reading abaut symptoms I don’t have them.My meds are the same as befor surgery. I am vitamin D deficience but my calcium levels are fine. My hormones are fine, MRI of a whole spine and brain is ok. Despite all the test I am still ill and still progressing. I am taking vitamin D, but not the one
that we get here in Slovenia, but I go for it in Austria our neighbour country. Because it is pure with no E. Our vitamin D has a lot of E and I had alergic reaction…., the same reaction my daughter had….she was swalling around the mouth and difficult swalloving. Sorry for mistakes in my gramar.
Agata
9 years ago
Hi Jason
Thanks for all the information. As I sad to Lucy…no inflamation….or rheumatological diseases, not genetic. I also tried prolotheraphy for ligament laxity….I did get inflamtion but no new tissue, someth8ng is simply wrong. It all looks to me the anasthesia never go out, but is in my tissue….maybe crayzy or not. When I asked alternative medicine…..they say the toxins go to connective tissue if there are too many of them. I read that tamarind is helping the body to flush fluor out. Or another product….natural one….vulcano dust….called Zeolit. I have tried zeolit but get upset stomac. I will try it again. Maybe too many toxins…i don,t know.
Lucy Sky
9 years ago
Hi Agata Just saw your posting about Tamarind and volcano dust . I will make some enquiries and get back to you.
Hang on in there.
Big Pharma can go and whistle.
Lucy
Agata
9 years ago
Hi
Thanks to all of you. My plane is also to go to other countries to get diagnosis. I am now waiting for second opinion from my insurance company. They will send all my medical records to best doctors…they say to Boston.
Lucy Sky
9 years ago
Hi Jason, Agata, Daniela, Debs, Lisa, Terri, Lucero, et al.
Just come across all this. Sorry but feel too upset to wade thru it all. Hope you can make sense of it all. I am sorry but I feel too upset .
When will the nightmare end?
I would gladly give evidence to get justice and see those individuals who are responsible for hiding the truth then continuing to push this terrible drug onto unsuspecting innocent people in prison for a long, long time.
Lucy.
US National Library of Medicine National Institutes of Health
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Abstract
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Drugs. 1993;45 Suppl 3:65-72.
Fluoroquinolones: interaction profile during enteral absorption.
Deppermann KM1, Lode H.
PMID: 7689454 [PubMed – indexed for MEDLINE]
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Similar articles
Evaluation of the influence of antacids and H2 antagonists on the absorption of moxifloxacin after oral administration of a 400mg dose to healthy volunteers.
[Clin Pharmacokinet. 2001]
Review Drug-drug interactions with fluoroquinolones.
[Pharmacotherapy. 1993]
Effects of magnesium-aluminum hydroxide antacid on absorption of rufloxacin.
[Antimicrob Agents Chemother. 1…]
Effects of iron supplements on the oral bioavailability of moxifloxacin, a novel 8-methoxyfluoroquinolone, in humans.
[Clin Pharmacokinet. 2001]
Review Pharmacokinetics of the newer fluoroquinolones.
[Pharm Weekbl Sci. 1987]
See reviews…
See all…
Cited by 5 PubMed Central articles
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[Can J Infect Dis. 1999]
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[Antimicrob Agents Chemother. 1…]
Pharmacokinetics of sparfloxacin and interaction with cisapride and sucralfate.
[Antimicrob Agents Chemother. 1…]
Hey Lisa, Have you noticed the new study about increased death rates among middle-aged Americans by Drs Deaton and Case due to pain medicine and alcohol poisoning?
“Recent reports of illness and disability might provide some clues. More middle-aged whites report that their general health is not good; and, more report chronic pain — neck pain, face pain, joint pain, sciatica. More report mental distress or mental illness. More say they have trouble walking a quarter mile or climbing stairs. More say they have trouble shopping or socializing with friends. More say they can no longer work.”
You need money and insurance to be able to “report” and get the prescriptions, which might explain the race bias.
Does anyone know what the contra indications are of chamolile please?
Hi everyone! Hope each of you are doing good. Just want to mentioned this here. I started seeing a doctor who has the same theory as Jason, that many Floxies got this way because they have Methylation issues and it could be key to some peoples recovery. Genes have alot to do with things like this. The way we detox, why he got sick when others never had a reaction with this drugs.
Sensitivity to noise, light , to smells, cramps, spasms of muscles esp the Achilles tendons, burning of legs. I hope that these people get put in prison. I have to see the out of hours drs in the morning to be checked over due to the chamolile drops given to me yesterday.
On a point of interest the camolile increased the burning and spasms. I wanted to know if anyone else had ever tried camolile and what their experience of it was.
I have just found out that garlic is contraindicated with warfarin!!!
What a night mare. Before being floxed I could eat anything.
Hi Lucy. These questions you asked last page about Adrenal Fatigue and Thyroid are pretty complex questions and issues, and all these things have once again many causes, please do not jump to any conclusions, proper testing is important before trying to discern the what and the why etc. Without testing, someone can have 15 or so symptoms of 15 or more different ailments, which all share many of the same symptoms, this is one reason why there is so much misdiagnosis out there everyday. You mentioned your Cortisol was only “slightly” elevated, it can fluctuate a lot as I mentioned before, and I am not sure how that was tested for you but let’s remember here the Hyperthyroidism, Insomnia, etc these things that you are struggling with are known causes of exhaustion yet again.
Having said all that, yes, IMO, Cipro “can” affect the Adrenals in many ways, there are numerous causes of AF, just plain old stress/anxiety is one of them, I know there are a lot of stressed out Floxies out there physically and otherwise, eventually this can take its toll on the Glands. There are other things that can happen here too related to Cipro (and others still that are not), Hormonal imbalances, Mineral/Electrolyte imbalances like Copper Toxicity which often shows up with AF (<=ME), Neural Transmitter imbalances, maybe more that's just off top of my head. Note also there are several "stages" of Adrenal Fatigue, and someone's symptoms vary depending on where they are at if they are going through it. What I eventually did was get a Hair Analysis test, this tests someone for Toxic Metals and many important Mineral/Electrolytes (the one I did was about 40 or so things tested. The other test I mentioned before is important too. I also had a Cortisol suppression test done but note this uses a fluoridated drug!
Does Cipro damage the Adrenals directly? I don't know, and I don't think anyone else does either as far as I know but I could be wrong on this, I don't recall seeing this anywhere however, and even if there is no info we have to remember no one knows the full extent of damage this drug does. Also note, I "don't think" AF itself is going to affect someone's Thyroid, I could be wrong on this too but really don't think so.
Treatment depends on the cause, what stage someone is in, etc again a good Naturopath will know these things, otherwise they wouldn't be that good IMO. If your Sodium is sky high and you take things to bring down your Copper, you can see how this won't be helpful, root causes! M.D.'s are the turkeys who treat symptoms, which is the WRONG way to treat patients! Without testing, if someone just starts taking supplements first off they might be wasting time and money since they may not have AF at all, 2nd they might make it worse by causing worse imbalances. I hope you see how important these 2 points are, and they apply to a whole lot of ailments, maybe all of them.
AF itself is actually just another symptom, not a root cause. First you can exhaustion for example as a first symptom noted, from there with testing someone might discover they AF, however they still need to know why, some of the causes are above but there are others still like too much stimulant use, essential Nutrition missing etc. In my case I am quite sure there were several causes, and this can get tricky; stress was eliminated long ago yet I still had AF, being stressed too long in "fight/flight" mode will drain your system, once your system is drained your body can start accumulating Copper as you may not be "using it" properly anymore, in my case I was at toxic levels which can then keep the Adrenals down as the Copper is then thought to be "unavailable", so I needed to bring this back into balance which I did (yes I treated myself to answer your other question). Here is the rub for me, the "root cause" was still not revealed until after all this, once my Adrenals started "functioning" properly again, now they are working TOO MUCH! I feel this through having "butterfly" feelings in my gut, which I am sure is excess adrenaline, and when it really gets excessive I can crash again. Here again there are several causes on why, it could be things are not yet fully balanced, an issue with the gland itself, others, or the most probable cause to me when I look back on my last 30 of almost 50 years of not feeling right, I have COMT/MAO Genetic SNP issues which basically means I often have excess Adrenaline and can get stressed out easily. I can tell you that now that they are working again, there have been several recent instances where Adrenaline went overboard and I crashed, and it was for something simple like a Tennis Match which is nothing stressful, you can see how important something like this is. I have not tested this last part yet to confirm this suspicion, but it makes the most sense.
This is not the best website but it is more basic than some of the others where things are more complicated, so its a good starting point.
http://www.adrenalfatigue.org/what-is-adrenal-fatigue#what-causes-adrenal-fatigue
As for the Thyroid questions, I replied to one of your messages 2 pages ago which I suspect you did not see. I will make another more detailed post for you about it soon.
Of course these are all my unlicensed opinions as usual.
Hi everyone- I’m sure this has been discussed to death but I just got my 23 and me results and wondering what program I should put them through so that I can understand this information. BTW I am 7 months out. Starting improving at 5 months out. Still have a long way to go. Thanks in advance!
Hello
My name is Agata and I 36 years old. In year 2013 I had back surgery…..herniated disc. Since the anasthesia my problems began. Al my joint are afected. The main simptom is that ligaments strech so easy and the joint is than unstable. I am living with a lot of pain and disabilities. It looks like I have connective tissue disease but I dont. It all started after general anasthesia, and the anasthetic was Sevoflourane wich is highly fluorinated. Could this be a reason? What test to be done? It is 2.5 years from surgery and it is still progressing.
Sory for mistakes in language. I from Slovenia ..Europe.
Does anyone know if there is any fluoride in clexane, marcain and or chamomile. BTW Chamomile is not recommended for various reasons, it is not tested thoroughly etc, etc.
Does chamomile adversely affect the heart?
Hi lucy
I am sorry for you but I can’t give you any advice because I am new in this. My simptoms began in year 2013 but I just now realised that must be fluor. Soo I can’t give you any advice because I am looking for advice too. But I am asking you, did you get any offical conformation from doctor that is fluor causing you this. Any lab test? Here in Slovenia they have no clue abaut that, or I am just so unlucky and the doctors I see are not the right one.
Hi Agata
Nice to meet you.
Yes I have a medical report stating the cause is due to antibiotics. I have had cipro on a few occasions but it was only 19 months ago following the prescribing of three antibiotics at ONCE when I was struck down with an acute attack.
Chamomile made things worse . It is under researched and under tested. it is contraindicated in people on warfarin and with epilepsy etc, etc.No doubt people will say the same about drugs as well. Just because something is ‘natural’ does not mean it is safe.
Sorry but I am going through a very rough time at the moment.
Debs & Lisa. Is there a list somewhere of all the Quin & Fluoridated & other closely related drugs somewhere? And a large list of what “might” be safe, including bluddy anaesthesia options? Lisa did you make an article before compiling them?
I have to admit I am a little bit terrified of getting into an accident of some kind, and being brought to the Hospital for surgery unconscious or debilitated, and then being given Fluoridated anaesthesia & quin related drug, good God.
The website above has a pretty comprehensive list of “F” drugs, but what about the Quin and closely related ones, and any other ones we know interact badly like Steroids etc. TIA
Hi Lucy, Daniela, Jason
I am very confused abaut my condition. Because here in Slovenia we don’t fluorinate our water, I have healthy diet because my brother has a farm and I am eating healthy home vegetabel, meat and other stuff, grown withaut any cemicals, pesticides and I was healthy befor with the same diet I have now. It all started after surgery and still progressing. My only simptom is ligament laxity, or I woud call it ligament strech syndrome and hyperrefleksia. And if I am thinking right that fluor in my body should be getting out and the symptoms would slowly stoped..but they are progressing. Why? If I am not getting any fluor in my body by the water or other stuff. They tested me for genetic diseases of connective tissue, and autouimmune and inflamatory. What the hell is going on?
Hi Agata Have you been tested for lupus? Some drugs can give you lupus, for example phenytoin, the ppi’s statins, antibiotics, have your anti nuclear antibodies and ebv -for glandular fever been tested? Have you had a double stranded DNA test done?
Are your temperature and heart rate normal?
What meds if any are you or have you recently taken.
Lucy
Dear Lisa
You may want to modify this .I don’t mind.
Please google local anaesthetic drugs and adverse reactions. Note marcain, inexpensive local anaesthetic drug et most cardio toxic LA as stated previously.
You may also wish to google anaesthetic agents with fluorines.
Think about dry cleaning agents that contain solvents too.
Anaesthetic gases contain solvents. For example Trilene.
HALOTHANE – this causes liver damage. Then we have entonox which can cause seizures and peripheral neuropathy.
Scary so may not wish to look it up. Sorry gang.
Lucy.
Has anyone else experienced their bowel movements being a bit “off” in terms of its color? I don’t have any pain and I’m pretty regular but it’s a very light brown to almost yellow hue every time. This has been pretty consistent since I stopped taking Cipro. I told my doctor but he didn’t seem at all concerns. Ran a bunch of tests and all my blood work came back normal. Liver functioning very normally/kidneys fine/etc. Is this sinply due to the bad bacteria being killed off? Or perhaps stress/anxiety?
Hi Lucy
I have been tested for lupus, They did ANA test, abaut glandular fever as far as I was reading abaut symptoms I don’t have them.My meds are the same as befor surgery. I am vitamin D deficience but my calcium levels are fine. My hormones are fine, MRI of a whole spine and brain is ok. Despite all the test I am still ill and still progressing. I am taking vitamin D, but not the one
that we get here in Slovenia, but I go for it in Austria our neighbour country. Because it is pure with no E. Our vitamin D has a lot of E and I had alergic reaction…., the same reaction my daughter had….she was swalling around the mouth and difficult swalloving. Sorry for mistakes in my gramar.
Hi Jason
Thanks for all the information. As I sad to Lucy…no inflamation….or rheumatological diseases, not genetic. I also tried prolotheraphy for ligament laxity….I did get inflamtion but no new tissue, someth8ng is simply wrong. It all looks to me the anasthesia never go out, but is in my tissue….maybe crayzy or not. When I asked alternative medicine…..they say the toxins go to connective tissue if there are too many of them. I read that tamarind is helping the body to flush fluor out. Or another product….natural one….vulcano dust….called Zeolit. I have tried zeolit but get upset stomac. I will try it again. Maybe too many toxins…i don,t know.
Hi Agata Just saw your posting about Tamarind and volcano dust . I will make some enquiries and get back to you.
Hang on in there.
Big Pharma can go and whistle.
Lucy
Hi
Thanks to all of you. My plane is also to go to other countries to get diagnosis. I am now waiting for second opinion from my insurance company. They will send all my medical records to best doctors…they say to Boston.
Hi Jason, Agata, Daniela, Debs, Lisa, Terri, Lucero, et al.
Just come across all this. Sorry but feel too upset to wade thru it all. Hope you can make sense of it all. I am sorry but I feel too upset .
When will the nightmare end?
I would gladly give evidence to get justice and see those individuals who are responsible for hiding the truth then continuing to push this terrible drug onto unsuspecting innocent people in prison for a long, long time.
Lucy.
US National Library of Medicine National Institutes of Health
Search databaseAll DatabasesAssemblyBioProjectBioSampleBioSystemsBooksClinVarCloneConserved DomainsdbGaPdbVarEpigenomicsESTGeneGenomeGEO DataSetsGEO ProfilesGSSGTRHomoloGeneMedGenMeSHNCBI Web SiteNLM CatalogNucleotideOMIMPMCPopSetProbeProteinProtein ClustersPubChem BioAssayPubChem CompoundPubChem SubstancePubMedPubMed HealthSNPSRAStructureTaxonomyToolKitToolKitAllToolKitBookUniGeneSearch termSearch
Advanced
Help
Result Filters
Abstract
Send to:
Drugs. 1993;45 Suppl 3:65-72.
Fluoroquinolones: interaction profile during enteral absorption.
Deppermann KM1, Lode H.
PMID: 7689454 [PubMed – indexed for MEDLINE]
Share on Facebook
Share on Twitter
Share on Google+
Publication Types, MeSH Terms, Substances
LinkOut – more resources
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•
Supplemental Content
Save items
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View more options
Similar articles
Evaluation of the influence of antacids and H2 antagonists on the absorption of moxifloxacin after oral administration of a 400mg dose to healthy volunteers.
[Clin Pharmacokinet. 2001]
Review Drug-drug interactions with fluoroquinolones.
[Pharmacotherapy. 1993]
Effects of magnesium-aluminum hydroxide antacid on absorption of rufloxacin.
[Antimicrob Agents Chemother. 1…]
Effects of iron supplements on the oral bioavailability of moxifloxacin, a novel 8-methoxyfluoroquinolone, in humans.
[Clin Pharmacokinet. 2001]
Review Pharmacokinetics of the newer fluoroquinolones.
[Pharm Weekbl Sci. 1987]
See reviews…
See all…
Cited by 5 PubMed Central articles
The new fluoroquinolones: A critical review.
[Can J Infect Dis. 1999]
Pharmacokinetics of gatifloxacin and interaction with an antacid containing aluminum and magnesium.
[Antimicrob Agents Chemother. 1…]
Pharmacokinetics of sparfloxacin and interaction with cisapride and sucralfate.
[Antimicrob Agents Chemother. 1…]
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The Risk of Fluoroquinolone-induced Tendinopathy and Tendon Rupture
Fluoroquinolone-associated tendinopathy.
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Management of Subclinical Hyperthyroidism
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