woensdag 12 december 2012

Fluoroquinolone next...

The ICD9 CODE is the code that doctors submit...   
Erin Spangler Wilson    11 december 20:56
The ICD9 CODE is the code that doctors submit on the Lab slip for diagnosis/symptoms as the reason for requesting lab work. Our magic number is 727.67 Fluoroquinolone Toxicity code. We are real. Ask for this when having a consultation with a doctor. The medical community is getting it.
====================================================================
http://dianegarcia-floxed.blogspot.nl/
===============
http://www.youtube.com/watch?v=D8-e3NA0wX8

=====================================================================



Quinolone Vigilance Foundation

http://www.saferpills.org/

=====================================================================
The Fluoroquinolone Wall of Pain




========================================================================

Uploaded on Jun 21, 2007
This is a video my family took after I was given 2 prescription drugs that should never have been given to me together. See my website at www.fqvictims.org



I don't drink, never have. It was the VIOXX that the doctor wrote with the cipro that did me in.
2 doctors agreed on this treatment - 1)Dr. Michael Pontari at temple university hospital - is known as a "hotshot" for prostatitis patients - NEVER see him with this condition - he is ignorant and dangerous. 2)Dr. Pregnish Desai from Allentown Pennsylvania - another BOOB urologist. Don't go to a urologist with this affliction. Take 1) Proscar and 2(Flomax) for the rest of your life -
full recovery.
---------------------------------------------------------------
There are MUCH SAFER drugs that will help people. They do NOT need to be exposed to these poisons with common infections. Your argument is very weak at best. I did not need Cipro at all. An older, safer antibiotic would have done the same thing, except now I wouldn't be permanently brain damaged.
=======================================================================


2003 -- Sick, poisoned by Levaquin & Avelox



http://blog.garymoller.com/2008/03/my-doctor-has-poisoned-me-with.html



>> I've been HEALTHY my entire life, the poison took that away from me but I'M STILL ALIVE!!!!

-----------------------------------------
Unfortunately millions will never be rightfully compensated, their lives destroyed, health permanently compromised. And these POISONS REMAIN on the market to cotinue their carnage. Tell me why.
Current litigation
  • Court in Boston (January 2010) accusing Johnson and Johnson of illegally paying 
    millions of dollars in kickbacks to Omnicare, one of the nation's largest
    pharmacies specializing in nursing home patients. In return, Omnicare nearly
    tripled its annual purchase of Johnson and Johnson's products; including
    Levaquin.
    There are also cases currently pending before the United States District Court,
    District of Minnesota, involving Levaquin. On 13 June 2008, a Judicial Panel On
    Multidistrict Litigation (MDL) granted the Plaintiffs' motion to centralize
    individual and class action lawsuits involving Levaquin in the District of
    Minnesota over objection of Defendants, Johnson and Johnson / Ortho McNeil.[121]
    On 6 July 2009, The New Jersey Supreme Court had also designated litigation over
    Levaquin as a mass tort and has assigned it to an Atlantic County, N.J., judge.
    The suits charge that the drug has caused achilles tendon ruptures and other
    permanent damage.[122][123] Additional lawsuits have also been recently filed in
    the Illinois State Court. Of a total of about 3400 cases, 845 were recently
    settled out of court after Johnson and Johnson prevailed in three of the first
    four cases to go to trial[124][125]
    On 8 April 2010 in the Beaumont Division of the Eastern District of Texas, a
    class action lawsuit was filed by Lisa Presley on behalf of herself and others
    similar situated against Johnson and Johnson, Ortho-McNeil Pharmaceuticals Inc.
    and Johnson and Johnson Pharmaceutical Research and Development LLC. (Case No
    1:10cv00200.)[126]
    The various manufacturers have countered these allegations stating that they
    believe that these drugs are both safe and effective antibiotics, well tolerated
    with a minimum of side-effects, that such reactions are rare and the benefits of
    such therapy outweigh the perceived risks.

  • ========================================================================



    ========================================================================

    http://www.ncbi.nlm.nih.gov/pubmed/16895667

     acute renal failure. General review about a case report with crystalluria due to ciprofloxacin].
    [Article in French]

    Source

    Service de néphrologie-hémodialyse, centre hospitalier de Troyes, 10003 Troyes cedex, France. richard.montagnac@ch-troyes.fr

    Abstract

    A 58 year-old woman developed an acute renal failure very quickly after ingestion of two 500 mg tablets of ciprofloxacin, without any other identifiable risk factor. Renal biopsy was performed. No sign of acute interstitial nephritis was observed but tubular lesions were found, accompanied by deposits of a brown-yellowish substance identified by infrared microscopy as a ciprofloxacin salt. The outcome was favourable. This observation gives the opportunity to remind the different forms of quinolone-induced renal injury and to discuss the possible ways for preventing renal side-effects related to the quinolone use.
    PMID:
    16895667
    [PubMed - indexed for MEDLINE]

    =============================================

    http://www.lawyersandsettlements.com/blog/been-floxed-by-levaquin-or-cipro-maybe-fleeced-too-06582.html#.UTko9CfpxrA.facebook



    Floxed. Sounds so innocuous—or at least like some casually tossed remark about the previous night’s escapades—as in “yeah, I got really floxed up last night”. But to the victims who have come to add the word “floxed” to their everyday vocabulary—and who are a part of the been-floxed wall of photos (aka, Wall of Pain, see pic) on the Facebook page, Fibroquins Levaquin—”floxed” is insiders’ jargon for having gone through serious adverse side effects from taking a fluoroquinolone drug. Getting floxed, therefore, isn’t like picking up a mayor badge over at foursquare—it’s more like a badge of camaraderie that ties fluoroquinolone victims together—better not to have it.
    Fluoroquinolones are part of a class of antibiotic drugs—i.e., drugs typically prescribed to treat bacterial infections such as urinary tract infections (UTI), ear infections, bronchitis, inflammation of the prostate, typhoid fever, salmonella, chlamydia, pneumonia, etc…so chances are, either you or someone you know has been prescribed a fluoroquinolone at some point. Fluoroquinolones are more commonly known by some of the brand names that get prescribed: Levaquin, Cipro, Floxin, Avelox, Noroxin, Tequin.
    So what is getting floxed all about? How do you know if you’ve been floxed?
    In 2008, the FDA added a black box warning to Levaquin, Cipro, Avelox and all fluoroquinolone-class drugs. The black box warning is for risk of tendon rupture and tendinitis—the FDA alert (7/8/2008) stated:
    Fluoroquinolones are associated with an increased risk of tendinitis and tendon rupture. This risk is further increased in those over age 60, in kidney, heart, and lung transplant recipients, and with use of concomitant steroid therapy. Physicians should advise patients, at the first sign of tendon pain, swelling, or inflammation, to stop taking the fluoroquinolone, to avoid exercise and use of the affected area, and to promptly contact their doctor about changing to a non-fluoroquinolone antimicrobial drug.
    The Levaquin stories we hear at LawyersandSettlements.com are real and heart-breaking—and for those who have been floxed, they are life-altering—and not in a good way. The victims who’ve started to band together on Facebook share their stories of lives shattered and forever changed: cane-assisted walking, wheelchairs, numbness, burning sensations, cramps and worse.
    And those who’ve been floxed are angry—at the FDA, at their doctors, at the pharmaceutical companies. Sure, they can try to file a lawsuit against Levaquin or Cipro—that’s what I’d be doing—but doing so won’t bring back their lives. And as such, one can only wonder if getting floxed is really akin to getting fleeced.
    susan ·
    I do not feel the word "floxed" is suitable. Reminds me of groupies... I would say we are VICTIMS as people who have become VICTIMS to these God awful antibiotics did not have to have their lives destroyed...Had the FDA and drug companies done their jobs and there not be a conflict of interest, many people would be enjoying their life...NOT THE HELL FROM THE ADVERSE DRUG EFFECT OF THESE ANTIBIOTICS. They only care about the money...Levaquin is on the speed shelf in the pharmacies....Where is there justice??? I want my life back!!! NOW............Amen.

    Joanna C · 110 weeks ago
    I was given Cipro and/or Levaquin a few times over the years, starting with (probably) my very painful and complicated back surgery about 2003. The day before surgery the lab uncovered a UTI and slapped me with big doses of (I think) levaquin. I am 73 years old and my contemporaries don't have the troubles I have. My knee replacements -- the right one required 4 surgeries and still is very weak, the left one is better but both of them hyperextend with no warning and occasionally the knee(s) slip forward. This makes me very prone to falling. I have lost biceps ligaments in both arms. My neck fusion has given way and now the top fused vertebra has slipped forward and rests against my spinal cord. My back surgery has finally begun to go to pot and the sciatica, etc. has returned. In other words, I'm in a wheelchair and unable to do much around the house. My husband is fighting Multiple Meyloma and if it weren't for a couple of our children who live in town I don't know what we'd do. I have entered a lawsuit (not a class-action suit but with a group of other victims.) This has been dragging along for abut 3 years -- maybe this is normal, but I'm in a wheelchair and in pain all the time. I'm not much help to my husband. I also have Charcots disease and I may lose one or both feet as a result of the collapse of the ligaments in my feet. I know there isn't anything you can do for me but I just wanted to add my story to all the others out there. I'm trying to keep what my mother called a "stiff upper lip" but my life isn't very much fun and I don't expect it to get any better. I hope I get a lot of money out of the lawsuit but I doubt it.

    0
    Paul C's avatar
    Paul C · 109 weeks ago
    I am 55 years old this week. I've been battling severe muscle fatigue and muscle pain and twitching since 2004. Been through Mayo and spent tens of thousands of dollars. Doctors look at me like a deer in the headlights. Finally put 2 and 2 together after talking to my cousin. He had ruptured his bi-cep from cipro. Told me how ill he had been with weakness and fatigue and muscle pain. I told him I'd been sick for 5 years without any diagnosis. I went back and looked at my history and found out I had taken levaquin a month before getting sick and had taken levaquin and cipro at least 8 times since in the last 5 years and was currently taking it for a sinus infection. I had never put the 2 together. I immediately quit taking it but the damage was done and I'm very fearful it's permanent. It's been three years and the symptoms have worsened. I'm on oxycontin for 2 years and have been suffering with the poisoning ever since. The depression and disappointment of being immobile is the worst. I can never plan anything and am in constant pain and anxiety. I was a jock growing up and a body builder in my my early 40's. Now I can barely walk across the backyard and have had to give up golf, hunting, shooting hoops, anything physical. People look at me and say "you look fine". It's hard for them to understand. This has to stopped to prevent others from the same fate. God help them.

    -----------
    Boo Radly's avatar
    Boo Radly · 104 weeks ago
    My floxing happened in a hospital- ADR started within hours - burning at IV port, then I could not walk, burning pains all over, blood clouts in nose, told nurses, they saw. Then I apparently started coding because they were running into my room - rapid heart rate, respiratory failure, wasting, etc. My doctors knew. They gave me 600 mg predinsone, NSAID's, blood thinners and antacids, depressants. I am profoundly deaf, no one is sharing what drug I was given nor why they are running into my room. Upon release, I who arrived with no pre existing conditions and on no meds, physically active, working, am now crippled, burning pains all over, purpura up and down my arms. I ask why - the doctors say bad pneumonia. It got much worse at home, no 2000 mg's of pain meds - I am scared I am dying of some strange exotic disease they did not catch. Finally I demand and am refused my med records - long story, long fight but I got them - looked up levaquin - it's all there. All doctors deny, new docs deny - hospital deny, every watch dog group I contact tell me - Levaquin is not black boxed and no drugs given concommitant to be worried about.....pretty big stone wall. The hospital even refused to correct my age as it is one year off - said they read the records and it's right...there is a little humor in that - hm, I know my birth date(only off by one year but they refuse to take my word). There were three days of some doctor scribbling all my failures into the record - this must be a profitable drug, at the cost of how many ruined, crippled patients and even deaths. I now know why a lot of ADR's are not reported - any govm't health care agency will refuse to review and will refuse to have you surveyed as required after a review. I want to take my records to a real attorney - know of one? I have lost the use of my left arm and hands - Ortho says tendinitis and most likely rupture, does not know why though, clueless about Levaquin. I can't work, drive, cook, walk my hearing dog, days are filled with nothingness - depressing and stress full. Wish it were not so and wish we could stop the maiming not to mention the deaths. I am 10 months out and feel like I can't face another day. You would be shocked if I told you how high I went with this and am told levaquin is safe and effective and, drum roll please, "standard of care" - I am over 60 not by much but it is mentioned. Standard of care is not giving a drug that is warned against giving a certain patient and certainly not with that poisonous soup of concomitant drugs that guarantees intensifying excruciating pains of ADR's. Standard of death more like it - if you don't die, you sure wonder if it would not be better. But, I'm not a professional board certified health care given. Like to warn people but seems like they can't wrap their head around it til it happens to them.

    Sad and unnecessary. PN pain burning like nothing I could ever imagine - I can no longer tolerate an injection or have more blood drawn. I am in more pain after a doctor's appmt - tests for range of motion and then be told they are clueless, lets do more tests....they all deny levaquin. It seems like they get permanent patients to run tests on an refer to a huge range of specialists. I went through that 8 months ago.

    But, I do have torn shoulder/rotator cuff, tendinitis and PN. I have a ProntoIII to race down the driveway in to feel like I am free again. I can't propel a non motorized one.

    Lsst word, I don't feel the FDA has American citizen's safety in mind anymore.
    ------------
    Teresa's avatar
    Teresa · 86 weeks ago
    I too agree with all of you, I am only 34 years old and have suffered tendon ruptures in BOTH ankles. I can not walk without braces and have already went through reconstruction surgery on the left. The injury has also caused back issue's that has required spine injections. I can not do much to care for my 3 children so it puts much added stress on my husband. I was never told about any side affects in the hospital before they gave me the medicine. In short my life will never be the same and me and my family suffer because I took cipro. It is so unfair and I can not find a lawyer to help.
    ---------------------
    Billie k alexander's avatar
    Billie k alexander · 74 weeks ago
    I have torn my rotator cuff almost totally off requiring extensive surgery of two orthopedic surgeons with repeated tears since. I have also torn both hamstrings, have extreme depression, along with extreme pai . Please help me find an attorney to help me.
    ---------------------------------
    erin wilson's avatar
    erin wilson · 68 weeks ago
    I know everyone on the above page, I am a victim as well. TWICE, It took me six years to recover from my first Levaquin and my second experience (14 months ago) made the first pale in comparison. No one can get legal help because the truly horrific symptoms are not recognized but an achilles heel tear is. What I wouldn't give for an achilles heel tear in trade for what Levaquin has done to me and everyone you see pictured on the above page. Our continual pain and suffering can not be documented on an x ray so there is no legal assistance for the unbearable pain of head to toe peripheral neuropathy, central nervous system damage, neuropsychotic damage, anxiety and depression, joint pain and swelling, not to mention the wide array of autoimmune disorders that have been triggered because all hell broke loose when we were given this Napalm of antibiotics. The worst part, not one person I have ever had contact with had a diagnosis that warranted the use of a drug that was designed for anthrax.
    --------------------------
    CJ Alexander's avatar
    CJ Alexander · 64 weeks ago
    I was given Cipro in 2002 for a bladder infection post hysterectomy. In 2004, I had the severe lung infection, ARDS, was hospitalized for 2 months, and during that time was given Levaquin as one of the antibiotics. Afterwards, again put on Cipro for infected bedsores (I was only 51). It's been 7 years, but I still suffer from peripheral neuropathy, joint swelling, and overall pain. My life has been turned topsy turvy. I haven't had a good night's sleep since then. My symptoms have stumped doctors, leading them to not believe me. Until today, I had no idea that my symptoms could have been caused by these drugs. I just wish there was a way to reverse all the damage.
    ---------------------
    Elizabeth's avatar
    Elizabeth · 59 weeks ago
    I took 4 pills cipro in Feb 2007 and have gone from an active healthy mom who exercised regularly to walking with a cane. I have had right hip surgery for a labral tear, cns, pns, autonomic and sympathetic nervous system, hearing, vision, and tendon damage. Not to mention temperature sensitivity, collagen degeration, digestion issues, candida overgrowth and the list goes on and on. I have spent well over $10,000 trying to improve my health and have heard over and over from Drs that a medication could not do this. Yet not one of those Drs could firmly diagnose what caused my health problems. Until the medical community recognizes this class of drugs can harm people we are on our own as far as trying to recover.
    ------------------------
    Amanda Myers's avatar
    Amanda Myers · 59 weeks ago
    Please read this with careful consideration. On November 17, 2011 I was prescribed Levaquin 750mg for 7 days for a suspected kidney infection. Four days into taking the generic of this drug, I had a severe allergic reaction and severe side effects. My allergic reaction was loss of breath and throat closure. My side effects were and some still are: hives, severe back and abdomen pain, burning sensations in skin/throat/esophagus/sinuses/eyes, high blood pressure with rapid heart rate, head and ear pressure and ringing, joint/muscle/tendon pain and popping, panic attacks and anxiety, short term memory loss (brain fog), insomnia and nightmares when I was able to sleep, water retention and swelling in hands and feet, tingling sensation in hands and feet, extreme fatigue, kidney pain, and painful headaches. My three children, ages 4, 5, and 9, have had to watch their mother become a zombie who could not even care for herself let alone them. Who had to have their grandmother come and take care of them for 2 weeks straight, because their mother could not manage to think at all or get up and do anything. Please help take this poison off the market for good! Thank you so much.
    Amanda Myers
    -----------------------------
    Matthew's avatar
    Matthew · 59 weeks ago
    I was prescribed Cipro in late March of 2011. I immediately felt some weakness in my left leg in between the second and third doses. For the next three days that was mostly my only physical side effect. I was also experiencing nightmares and night sweats but did not attribute those to Cipro. Day 4, was a Friday and I was eating lunch with some coworkers. I started feeling immense pain all throughout my left leg, upon trying to get up to leave I was unable to. Pain level was at a 9 out of 10 consistently after that. Body felt like it would rip in multiple places. I got a lot of paralysis in my arms as well as my fingers. Sleeping became non-existent as my knees felt like they would explode at night and both Achilles felt as though they were seconds from tearing. The pain was unfathomable. 9 months later still in extreme pain and living is just surviving.
    --------------------------
    Denise's avatar
    Denise · 53 weeks ago
    I was just prescribed Cipro last week end..I woke up 2 days after starting this drug with such severe hip pain thatI could hardly walk, I have mild osteo disease in that hip but it has not hurt in over 5 yrs since I quit the work that I was doing however it NEVER hurt like this before, I was sitting on my couch today (because that is about all I can do) and my toes started to hurt, my arms and legs feel like they weigh a ton........Good Lord no one warned me about this stuff..
    ------------------
    jon mulder's avatar
    jon mulder · 42 weeks ago
    my wife was diagnosed with a UTI, was allergic to levaquin,, sent home suffering a stroke that was missed inn diagnois in ER nuerolagist showed me she was having a stroke when sent home 1 day after admission. I was to calla the doctor if medicine for UTI was not working, called him and gave prescription for levaquin 500 MG. Gave her two doses, got worse each day, ended up with a horibal sscerne in the bathroom,back to hospital where the neurologist said the horse was out of the barn and he could nothing to stop it she lost sight, lost abillity to talk and finally died 2/18/12. I have it in the hands of myj attorney, and we see what happens, will advise
    ------------------------
    Tracy Will's avatar
    Tracy Will · 41 weeks ago
    I took Levaquin for 9 days for Bartonella and each day the tendons in my Achille's heel got worse and worse until I could barely walk at all. I stopped the Levaquin after learning it could be related, but the pain did not stop. I was in severe pain for about 9 months. It finally started to clear but it would recur over and over again, and it still does. The achilles tendons will get sore and stiff, achy and I will have trouble walking. The pain is there even when I am just laying in bed. It affected my knees too and that recurs on and off as well making it hard to walk and extremely hard to climb stairs, and my knees give out too.
    --------------
    Sue's avatar
    Sue · 41 weeks ago
    I was on Cipro for 2 months and found out I got a stress fracture. They are blaming it for the breakdown of hte muscles supporting the bones in my foot. It took a longer recovery do to the Cipro in my system once I stopped it. I also experinced severe muscle cramping too. I was on it for Lyme Disease.
    -----------------------------
    Bill Jackson's avatar
    Bill Jackson · 36 weeks ago
    A year after taking Cipro, I suffer from irregular heartbeats, oversensitive to light, cracking joints, insomnia. The official warning says less than 5% of users suffer bad effects. That is a lie - I know two people who took it and BOTH suffered bad effects.
    --------------------

    My name is Kelly, and I was prescribed levaquin 500mg for 14 days, but stopped on the 12 day because i was so sick and wanted to feel better for christmas. That was December of 2007, Little did i know five years would pass and at the age of 26 id still be completely sick and ruined by this medication. My symptoms and story are too detailed to list everything out, but the... nightmare caused by this drug began with full body tremors and hand tremors so bad to the point that i could not even write or type or hold a glass of water. Nightmares, nightsweats, ringing in my ears, intense bone pain, terrible adrenaline surges that went up and down my arms that felt like i was injected with speed and needed to run a marathon which i still get to this day, mostly set off by foods that levaquin has left me allergic to, vertigo and dizzness, waking up with what i suspected were sugar lows and highs, too many mornings i woke up and could barely walk because the room was upside down and i had severe vertigo- i finally bought a sugar tester and sure enough fmy sugars were 42 upon waking(thought i was going to die) and 240!! My sugars had always been normal and blood tests always showed fine at around 80-85. My pupils dialated and then would constrict and wouldnt stay one size, my body became so dry and dehydrated, dark urine, cracking joints, knees, wrists and neck the worst-recent xrays confirmed arthritis and degeneration of knees, what healthy person in their 20s gets arthritis and degeneration?Anxiety, depression and panic, Rapid heartrate(tachcyardia) worst upon standing goes from 74 sitting to 130+ standing, laying down 42-48bpm, high blood pressure readings, severe food allergies caused by levaquin. I am now severely allergic to milk, eggs, and wheat amongst many other things. Eating any one of those things sends my body into a crazy response leaving me shaking, adrenaline surges and feeling like im in my last minutes. For the first three years i switched my diet to a more vegetarian type diet but that left me feeling even more weak and in need of healing foods. I currently am following a diet that closely resembles the paleo diet and my diet basically just consists of grass fed beef, wild caught white fish, organic vegetable fed chicken, organic vegetables and fruits such as squash, broccoli and cauliflower, asapargus, carrots, and a few select berries such as blueberries and strawberries. Even some of those foods make me sick and i have a very hard time affording the high price of keeping myself at a somewhat functioning level by having to eat this way. I have spent thousands upon thousands of dollars on tests, drs, and food trying to find an answer or cure without much success. I have tons of documentation. My best advice is to change your diet , avoid all alergenic foods sucj as milk, eggs, soy, and wheat, or better yet if you can afford it get a food allergy blood spot test and see what damage levaquin has caused your immune system to start targeting certain foods so you know which are problematic, make sure to get lots of fresh air and walks if you are able, and surroud yourself with supportive people, even if its just people from the fq boards who will lend an ear. I know how difficult and depressing it is to have no one understand or believe this illness. I feel very lucky to have some close people in my life who support me including my fiance who has been one of my biggest support systems.i recently got pregnant , and had a miscariage at almost 2 months. I blame levaquin as i know my body was not functioning correctly for the pregnancey and my limited diet due to levaquin most likely was not providing the correct nutrition. I am unable to tolerate any supplements as they make me so sick and feel so weird. I have experienced so much more then id like to plaster on facebook, but you can contact me and i will share more of my ongoing struggles with you caused by fluoroquinolones. I wish you all a healthy recovery, and i am posting a link to a video i made on youtube back in 2008 in hopes to spread the word about fluoroquinolones and posibbly make a difference even if for just one person in search of what was happening to them.

    http://www.youtube.com/watch?v=ugQnSLY-pzw&feature=youtube_gdata_player



    ....Sponsored by: Stevens-Johnson Syndrome Foundation  The FDA should implement a mandatory adverse drug reaction reporting system by physicians and hospitals of all cases of Stevens-Johnson Syndrome (SJS) and Toxic Epidermal Necrolysis (TEN)




    ever i was Chief Cook and manager of Restaurant i earn i lot of money and have much prestige 
    ,,,,,,,,,,......
    Don t take Avelox, and other FQ !!I was poisoned with Avelox + Tarivid (and more fluoride Drugs with Prozac I had extreme high, palpitation and high blood drug so high that my brain are damage, I had with Prozac nosebleed, blood on my right ear where the tinnitus is hallucination, suicide idealization and thoughts, was aggressive .. did everything broken home
    normally I never dot this ,with antidepressants though!

    in 2005 was the laste and stronger poisoning Avelox and Tarivid , I have tinnitus, 6000 hz and more then 45 - 60 decibels, liver damage, severe headache, muscle aches, strong dizziness , severe vertigo , i am NOT from natur now i lost everyting and be depress , i can t never work again is so
    sad i was one very good creative chef cook 


    first time i am floxed whit prozac in 1994 . Prozac the most !
    and there give Fevarin to ..and maybe more the fucking corrupt bastard doctor refuse to give me my file 

    i can t do one serious investigation
    then in hospital 1995 whit antibioctica but i don t know the name which .
    in 2005 avelox 400mg ,3 day , 1 for day the third day I was destroyed
    the seems  month the give me Tarivid !!!

    http://destruida-los-restos.blogspot.com.es/

    http://en.wikipedia.org/wiki/Ofloxacin

    my fucking doctor, falsified my file in hypochondria
    my EX partner (women)  and my Daughter leave me in 2007 i am alone all 7 year 

    now is 2014 >>  :  CLIK ONE TO LISTEN MY TINNITUS SOUND

    Tinnitus info







    =====================================================================

    Prosac Bijwerking !!!

    Fluor !!


    Uploaded on Dec 14, 2009
    "I say this in all earnestness and sincerity of a scientist who has spent nearly 20 years research into the chemistry, biochemistry, physiology and pathology of fluorides. Any person who drinks artificially fluoridated water for a period of one year or more will never again be the same person."

    Charles E. Perkins, research scientist with 20 years experience with the chemistry, biochemistry, physiology and pathology of fluorides

    ik heb een empty sella
    http://www.ntvg.nl/publicatie/het-39empty-sella39-syndroom-als-oorzaak-van-panhypopituiumltarisme/volledig

    Fluoride Danger picture google
    http://tinyurl.com/a6rr2m9

    Fluoride is een bestanddeel van rattengif en één van de basisingrediënten van zowel Prozac (fluoxetine-hydrochloride) als het zenuwgas Sarin (methyl-isopropyl-fosfonofluoridaat). De meeste mensen poetsen er elke dag hun tanden mee.
    ik heb PROZAC &  AVELOX

    DAAROM HEB IK NU EEN EMPTY SELLA
    EN MOET BIJ DE ENDOCRINOLOGE


    Natriumfluoride
    Eind jaren 1990 deed Dr. Jennifer Luke van de Universiteit van Surrey onderzoek naar het effect van natriumfluoride op de pijnappelklier. Ze stelde vast dat de pijnappelklier natriumfluoride als een magneet aantrekt en absorbeert. Vervolgens treedt calcificatie op als gevolg waarvan de hormoonhuishouding
    verstoord raakt.


    De pijnappelklier, ook wel epifyse, glandula pinealis, epiphysis cerebri of derde oog genoemd, is een endocriene klier in het brein.
    Deze klier produceert melatonine uit serotonine, een hormoon dat invloed heeft op het slaap-waakritme en het voortplantingsritme.
    De kleine klier in de vorm van een pijnappel bevindt zich dorsaal van het corpus callosum (de hersenbalk) en aan de bovenkant van de derde ventrikel. Bij hogere gewervelde dieren heeft het zich ontwikkeld uit het zogeheten derde oog.

    http://www.bovendien.com/gezondheid/gezondheid/het-effect-van-fluoride-op-de-pijnappelklier

    =======================================================================

    http://www.cbg-meb.nl/CBG/nl/humane-geneesmiddelen/actueel/20080724-moxifloxacine/default.htm

    actueel geneesmiddelen voor mensen

    24 juli 2008 - Beperking gebruik moxifloxacine  !!! (  Avelox )

    Moxifloxacine bevattende geneesmiddelen voor oraal gebruik mogen alleen in bepaalde gevallen worden voorgeschreven. Dit heeft het Europese agentschap voor geneesmiddelenbeoordeling EMEA geadviseerd na een herbeoordeling van de veiligheid van moxifloxacine.
    De EMEA concludeert dat moxifloxacine bevattende middelen voor oraal gebruik uitsluitend mogen worden gebruikt bij acute bacteriële sinusitis en acute exacerbaties van chronische bronchitis wanneer andere antibiotica niet gebruikt kunnen worden of hebben gefaald. Bij buiten het ziekenhuis opgelopen longontstekingen mogen ze uitsluitend worden gebruikt wanneer andere antibiotica niet gebruikt kunnen worden.  Tevens wordt geadviseerd de waarschuwingen in de samenvatting van de productinformatie aan te scherpen.
    Moxifloxacine is een fluorchinolon. Het wetenschappelijke comité van de EMEA, de CHMP[1], waarin ook het CBG is vertegenwoordigd, heeft alle beschikbare informatie over de veiligheid van moxifloxacine-bevattende oprale middelen opnieuw bekeken. Aanleiding hiervoor waren zorgen over de veiligheid voor de lever bij het gebruik van deze middelen in de hiervoor genoemde indicaties.
    Meer informatie staat in het EMEA-persbericht m.b.t. orale, moxifloxacine bevattende geneesmiddelen en het document 'Vragen en antwoorden over het advies om het gebruik van orale toepassingen van moxifloxacine bevattende geneesmiddelen te beperken'.

    ======================================================================

    http://www.yourlawyer.com/topics/overview/avelox_liver_damage

    Adverse reactions to fluoroquinolones may occur almost anywhere in the body. In addition to occasional unwanted effects on the musculoskeletal, visual and renal systems, the drugs in rare cases can seriously injure the central nervous system (causing “brain fog,” depression, hallucinations and psychotic reactions), the heart, liver, skin (painful, disfiguring rashes and phototoxicity), the gastrointestinal system (nausea and diarrhea), hearing and blood sugar metabolism.
    The rising use of these potent drugs has also been blamed for increases in two very serious, hard-to-treat infections: antibiotic-resistant Staphylococcus aureus (known as MRSA) and severe diarrhea caused by Clostridium difficile. One study found that fluoroquinolones were responsible for 55 percent of C. difficile infections at one hospital in Quebec.

    =======================================
    www.youtube.com/watch?v=BvEizypoyO0&feature=share

    ========================================================================

    Geen opmerkingen:

    Een reactie posten