Pockets symptoms and conditions

MIRENA SHOULD BE PULLED FROM THE SHELVES!!!!!!! THIS IMPLANT IS THE DEVIL............. In August when I had the Mirena put in, my hair was my best feature. I am 33 years old and all my life people have commented on it. I had a full head of thick blonde hair. Now I have an appointment next week with a dermatologist to see if there's anything I can possibly do to get some of it back. I lost enough in the shower over the past 2 months that I could have made someone a week and that I had to call a plumber. What I should do is carry my tail to see a a LAWYER. My mood swings have run rampant, I've gained weight eating like a bird, I have the cramps from hell, and the littlest thing ticks me off. I told my doctors office that I knew it was the Mirena and they said "Oh you've had a baby, this happens." Hello? My daughter is a year old. And I don't think I should be going bald after giving birth anyway. I think they just want to keep their pockets lined and that's the politics of medicine. Ladies thinking of getting one..........DONT DO IT!!!!!!!!!!!!!!! Keep your hair!!!!!!!

After you read a representative sampling of this website's testimonials, you certainly ask yourself inter alia: Can this be true? Did thousands of people inject an antibiotic from the fluoroquinolone family, which crippled them for longer or for shorter? Most of us, I suspect, never really get beyond the initial litmus test: Did this medicine poison me or save me? (The answer depends, of course, upon the age, gender, medical condition, and most importantly, the DNA make-up of the individual patient. For hundreds of thousands of patients this antibiotic is a boon. For thousands of other misfortunes this antibiotic is a disaster.) But there is another important question here.

Who gains from self-revelation? To be sure individual sufferers gain certain emotional catharsis from posting their adverse drug reactions (ADRs) to levaquin. E-postings are one-way anonymous tracks that form ruts on a well-traveled trail of tears. Unless these postings are hoaxes written by mischievious gnomes, then they consitute prima facie evidence for a causal link between levaquin injection and sundry crippling ADRs.

Curiously, this e-forum cannot be used as a tool for organizing thousands of potential litigants who might coalesce under a class action lawsuit. Yes, we can analyze each other's anonymous revelations to see if they muster our respective sense of the "ring-of-truth" re: levaquin toxicity, and we may contact each other one-on-one, but no-one can harness this intoxicating communication's technology to reach simultaneously all respondents en masse as a bloc.

So, who wins? The emotionally unburdened e-poster who learns belatedly that s/he is not alone and that prescription medicine likely caused more pain than the underlying malady for which s/he is being treated? Or big pharma that continues to manufacture and market a medication that poses downside risk to many consumers who unwittingly incur more damage than therapeutic value?

Indeed, who wins in a forum where consumers anonymously reveal their symptoms and unconfirmed suspicions? The answer is big pharma wins. Pharmaceutical companies data-mine our postings to estimate the frequency and bredth of ADRs about which consumers complain. House statisticians estimate the ratio of active complainants : silent complainants, i.e., the ratio of complaints who show up on this website to the far heftier percentage of complainants who never post on this website because either they are technology-challenged or they are incurious. House actuarians proceed to estimate how much operating profits their employers must set aside to cover losses in out-of-court settlements or in awards made to plaintiffs in class action lawsuits.

I think this is how the game is played in a behavioral sink where billions are made in a deregulated marketplace that allows predators and prey to interact anonymously. Sorry to be such a downer, but I fathom only the desperate plight of tens of thousands of levaquin consumers for whom no monetary award ever will compensate them adequately for their suffering, and the hundreds of millions of dollars at stake in court awards if consumers ever brought to bear their aggregate numbers and draw a bead on their big pharma tormenters.

I think it a true horror and shame that pharmaceutical companies have not devised a test which determines in advance which patient safely may consume levaquin and which patient's DNA places him or her at risk. I suspect the genome technology is available, but would dig too deeply into big pharm's bottom line. The economics of "parachutes-for-everyone" is infeasible. We are all guinea pigs in a B-grade movie featuring Russian roulette, billion-dollar pay-offs, and an FDA that pretends not to know.

My mother took lisinopril and she developed the persistent cough many experience. It was so severe that she went to the ER. While she was there, they told her she had fluid retention in both lungs and didn't link this drug to the fluid retention. Instead, they told her to get a biopsy for the possibility of lung cancer. More money in their pockets for tests and biopsies? Definitely!
I definitely see the link between the drug and the cough and the fluids in her lungs. Now,she's not on that medication but she is still dealing with side effects and I feel that all these medications they tell her to take are just making her worse. Has anyone just stopped all the conventional medications of high blood pressure and perused alternative treatments with success? I'm hopeful to find out what options i have that can cure her situation instead of leaving her at the same hopeless stage of dealing with terrible side effects.

I have been taking Lipitor for about 6 years suddenly developed a rash on my shoulders and chest. My doctor diagnosed SCABIES!!so I treated myself for that then the rash progressed so I had a biopsy done and after 3 months of agony my slin specialist had taken me off Lipitor as theh test showed a reaction to a drug. I am still itchy prickly and burning on arms legs and hands and cannot tolerate cortisone cream so am on tablets for a week..can anyone relate to this condition? My scalp is also very dry and scaly.

I had a bulging disk and a pinched nerve and was put on PREDNISONE - 60mg for 5 days, then 40 mg for 5 days and then 20 for 5 days. I had a round face to begin with, which I always hated, but now, my face just looks like a balloon that someone painted a face onto. I have a huge face, a double chin, huge stomach, I look 5 months pregnant and I absolutely HATE myself on this drug. I've been off now for a week and nothing has subsided except the sweats -- very embarrassing! I work and in the middle of a meeting, I sweat so badly that it rolls off my giant red face in rivulets. I'm just miserable. Does anyone know how long it takes to get rid of the side effects of this demon-drug?? I want to stay in the house and hide.

My daughter is now 20 years old. she received her 1st gardasil shot in 3/08 and the second in 8/08. She didn't get the last one and will not be getting it. From the day she got the first shot we should have known something. She nearly fainted immediately after both shots and complained of weakness and flu like symptoms. Started feeling poorly in the days and weeks to come. It was the end of her senior year the doctor tested her for mono. and it was negative but she had an extremely heavy schedule at high school. He chalked it up to the stress of that. Between the two shots she started having numbness and pains in her hands,elbows and arms. She continued to feel poorly and terribly irritable in the upcoming months. We saw a orthopedic doctor for her pains in her arms. He referred us to a neurologist. She was beginning her first year of pharmacy school and we put off the neurologist because she didn't have much time until spring break. During her 1st year of school after her 2nd shot. Her personality changed completely. Became insecure, moody, very anxious , constantly complaining of flu symptoms, bladder infections and had a hard time urinating. When my daughter returned home from her first year away at college I knew immediately that she had changed. She had been a very bright, intelligent, independent daughter and came home the daughter from hell. I couldn't believe what I was seeing. She was miserable, disliked pretty much everything. I had been talking with the doctor and friends over the course of the year and they all said that she was in a very stressful field (pharmacy) and college life takes some time to adjust. Then just a few weeks home from college she was complaining of dizziness, light headedness, headaches and saying she was having an episode. I thought maybe low blood sugars.....until I witnessed one. She was having Myoclonic seizures. She could feel them coming on but couldn't move or react. By the time I witness one of them she hadn't slept in 3 days. She was diagnosed within a week seeing a neurologist and having 50 to 60 a day. It took 4-5 weeks to get them under control in and out of the hospital . She has been on many seizure medicines it seemed like if it worked to stop the seizures she had crazy side effects. She was diagnosed with Juvenile myoclonic epilepsy. No one in our family has ever had seizures. I asked about the shot right away everyone said no and it was dropped. Since last July 08 we have been trying to help our daughter get her life back and it has been the worst year of our lives. She was unable to return to pharmacy school. The first fall 08 she was completely disabled. It looked as if she had had a stroke. They were saying it was the meds or maybe she had a breakdown of some kind. I am learning that it was side effects of this horrible shot. This is why I am posting this lengthy message because I wanted to let other people know that you and your daughter are not crazy!! We just started 2 weeks ago investigating the possibility of the gardisil shot being the reason for this madness. We have learned many things and are very sure that it was the shot that change our daughter.. I was contacted by a friend of a friend about a similar girl having the same pains in her arms and the focal seizures. I am learning more and more everyday about similar situations.. If this information can help one person it was well worth the time to jot it down. I will be praying for all of your families out there dealing with side effects from this vaccination.. I will let you know what we hear when we visit the neurologist at the end of the month. Any comments or information that may help us help our daughter can be sent to ******

My mother is on levaquin for a urinary tract infection which had gotten worst than we thought . The infection had set up in pockets behind her rectum. She is on levaquin, and other medicines such as; digoxin, metoprolol, lipitor, diltiazem and lasix. I am so afraid she is on medicines that can do more harm than good. She also suffers from congested heart failure. After she returned home from the hospital stay she extremely weak, is this a results of taking the antibiotic ( levaquin or a combination of all of the drugs listed above)?

Was on Prednisone for 11 days for an injury to my neck. I knew nothing about the drug except what my doctor told me that it would reduce inflammation in my neck and help with pain.

Well, it did nothing for the injury and pain in my neck. BUT.... I had HORRIBLE menstrual cramps and got my period 8 days early. I've had my period for 9 days now AND terrible pain in my upper left leg. I thought the pain was related to my leg and as the days went by I realized it was in my left hip! It's so bad I can't lift my leg without extreme pain. I KNOW IT'S FROM this awful drug.

I've been off of it for 4 days and the pain is still with me. I called my family dr. and was told Prednisone doesn't do that. BULL!! The paperwork I got with it from the pharmacy show "Changes in menstrual periods" "muscle/joint pain" "bone pain".

I wish I knew this BEFORE I ever took it.

Does anyone know if these symptoms and problems will go away after stopping it? I called the pharmacy and was told it will take 2-3 weeks for it to get out of my system!!

Has anyone had problems that eventually went away after stopping the drug?

Thanks and I hope everyone else is okay soon! This drug should be off the market. I received no help for my neck pain at all!!

I am currently taking the z-pak, on my third day. Today I woke up with white "pockets" under my tongue. Thinking about not taking any more. They are very painful. Hurts to eat or drink. I've taken this before but never with this kind of reaction.

About a month ago I was given Levaquin, for Pneumonia. After about 5 days my face and neck swelled up, Then came the Prednisone at the hospital. I have never in my 38 years not been able to control my own body. I do take Zoloft,and Xanax for anxiety. No one said I would have a problem walking (legs are not working properly) eating,sleeping, Buzzing in my head. Unable to lift my 3 year old let alone care for her, I get extremely fatigued easily. My Husband has missed a week of work, and if your like us....NOT GOOD. Even trying to type is hard I must look at every letter, It's like I REALLY have to think to make my body move.My kidneys feel like balloons in my back when I lay down,Uncontrollable crying. I can't believe this has happened. We have been going through this the whole month of May.Is anyone able to control the shakes? Even my head is shaking??? I suppose if I had tried hard drugs ever, this might be what it's like. I Pray someone can help me. I am so afraid of what is happening to my body. By the way, when they put me on the Prednisone they did not give me a taper... Had to see another Doctor for that. So as I sit here today, hands shaking, head shaking, knees feeling to loose to walk on them, Hard to breathe, or even to think the way I could a month ago. SOMEONE PLEASE HELP ME...

I've been taking 150mg of topamax a day for the last 10 months for trigeminal neuralgia. I haven't found any improvement in terms of appetite or memory in this time. Side-effects haven't lessened at all. Tingling in feet and hands, emotional instability including anger and grief, cognitive impairment in terms of slowed though-processes, spelling problems, and general intellectual functioning haven't improved with time. It seems as though I'm still walking in a haze all day long. I can pass ridiculous amounts of time by just staring into space and thinking about nothing. It scares me sometimes but it's taken away a lot of the pain and has allowed me some sort of normality. I'm 28, I want to live and work and build something for myself. So, for now, it's a trade-off .... side-effects vs life with pain or jumping off a balcony with my hands in my pockets some night when I can't take it anymore. It all comes down to the degree of debilitation that your particular disorder imposes and your ability to deal with it. I couldn't physically handle the pain or isolation anymore so I opted for the side-effects. I just wonder what the long-term implications of Topamax will turn out to be in five or 10 or 20 years from now.

Stop taking drugs while pregnant!! Here, in the US, they kill our babies by making then sick through these drugs. In old times women were not allowed to take prescribed drugs while pregnant. There's a nutrition issue that can help you diminish nausea. But please, stop injuring our babies and make pharmaceutical industry get richer. They don't care about your health, but their own pockets. Please, be smart, and use old-fashioned recipes of herbs combined with nutrition. Trust me, it will help you keep your and your babies' health well. God bless.

I posted several months ago on this string and wanted to update. I had bloodwork done for the 1st time since I quit the 20mg of Lipitor in August. LDL went from 123 to 210. Total Chol went from 191 to 285. HOWEVER all shooting pains I had been experiencing in legs, feet, and chst are GONE! Went back to my Dr. today, told her that same result and my serious objection to taking any kind of statin and she prescribed CRESTOR while telling me it was more potent than Lipitor! WTF!!!

I refuse this course, am drinking 30 - 40 ozs. of water each day now like I should have been, doubled my CoQ10 to 200mg/day, finally getting back into the gym to lose weight and get the HDL up from the level of 36 it is now. also started to drink the new yogurt type "shot" of Promise for cholesterol that provides 2 grams of plant sterols per day.

I will not take statins ever. I WILL find a natural way to keep my Chol under control. I've also been convinced that you don't have to be at or under the 200mlg of total chol to be healthy. Look at your C Reactive Protein and Homosiytes (sp?) If they are in range you should be good.

I know Lipitor was the cause of my rupturing each of my Achiller tendons a year apart while playing tennis in my late 40's Muscle pain soon followed.

My mother is 40 yrs old and has RA and gets remicade treatments through an iv . It seems to help with the pain of her RA, but the side affects are out of control!!!! she has white puss pockets that show up on her hands and feet. She was told that that was her white blood cells dieing from the treatment. her hands and feet peel and swell making it hard for her to walk or touch anything. her throat has these awful spasms that make it hard for her to eat or drink anything. Theres so much more, it would take all day to explain! Is this really the price she must pay for RA relief??????

I have lost 20 pounds in two weeks. I must sow up them holes in my pockets

Numerous side effects including but not limited to: spontaneous tendon rupture (right distal bicep), CNS agitation accompanied by anxiety and panic, extreme fatigue, digestive problems, on-going fluctuations of blood sugar level, rapid changes in body temperature, nausea, etc.

Some here insist on reporting the "good" this stuff has done (other than lining some peoples pockets with profits). I disagree. As I post this I see 2250 adverse effects have been posted previously. I urge yo all to look deeper ask the question: "Why so many problems with this class of drug?" The 2250 number is only for Levaquin..... don't forget to add in all the responses for all of the other drugs in the quinolone family. And while you are at it, find out how many other drugs have death as a side effect and how many have been reported. This is a defective drug.

It is my opinion that the pharmaceutical companies are experimenting with our daughters. There is no reason for anyone to get this shot. However, people have "bought into the idea" that they need it because of all the advertising by big pharma. The shot is good for one thing: the pockets of big pharma. These vaccines have not been proven safe. I will never let my daughter get this shot. God bless and good luck to everyone who is suffering at the hands of the pharmaceutical companies.

All that I can say is anyone taking this medication, be prepared. I am 24 years old and was diagnosed with Crohn's disease. I was in a severe flare up and was prescribe Prednisone. I looked like a balloon in the Macy's parade. Along with looking like I was 500 lbs in the face I was a woman on a rampage. I would blow up at the drop of a hat. I could not sleep, I was not the person to be around. Even after I was taken off of it, it took some serious time for me to be back to my normal self. This is an absolutely HORRIFIC drug and whomever invented it should be jailed for what it does to the people taking it.

I have been on BC for about 4 years and was last on Ortho. So when I told my GYN I wanted to be back on BC, she said that FEMCON FE was just like Ortho and to take it the exact time everyday. I found it strange that she told me that I had to take it the same time everyday; something I did not have to do on Ortho. So after taking it the first week and still experiencing bloating and other side effects I thought nothing about it. However, when I took my pill later than scheduled two days in a row, I started bleeding. In addition to the bleeding I developed other side effects...same as mentioned by others. After various comments from co-workers about my complaints that were very similar to pregnancy symptoms, I became very concerned and decided to research this pill. After finding this site, I immediately stopped taking the pill. It's been close to 3 weeks now since stopping and I've seen a world of difference. I am done with BC pills, condoms will just have to do. I already suffer from migraines so that is the only debilitating, uncontrollable issue that I am willing to deal with right now.

I am also convinced that GYN's are making their pockets fat by pushing this BC with their patients...a theory that does not sit well with me, because I had a lot of respect for my GYN before she prescribed this packet of side effects to me.

After being on Synthroid for a few years and getting NOTHING from it, I was switched to Levoxyl for several more years, and got NOTHING for it either. They are some of the most useless medications ever made, and all they do is put money in the pockets of the maker. Armour is what made a HUGE difference in my hypothyroid. ******

Wow! I just read many of the messages posted here and I am amazed. This is my second month on Femcon FE and it has been great so far. I tried Loestrin 24 and it was terrible. I bled ALL the time!. With Femcon FE, I don't have breakthrough spotting. Well, the first month I did, but it was VERY light. Now it is completely gone. Also, I've LOST weight since I've started this BC. I'm very pleased with Femcon FE, but I wanted to read more about it. I do believe that drug companies have doctors in their back pockets. Doctors push certain drugs for profit and disregard or minimize the signficance of negative side effects so I wanted to do my own research. In reading these posts, I'm almost terrified to keep taking Femcon Fe. But it's performing very well for me, so I'm going to continue it. Best of luck to everyone in finding a BC that suits you.

I took Singulair for a little over a year. In that time I have quit my job of six years, dropped college classes that I was previously excited about, and generally didn't give a damn any more about anything. My dreams became dark and horribly violent nightmares leaving me shaken throughout the day. I couldn't concentrate and was thinking I should seek professional help. My wife was worried that it was her and I couldn't figure out what my problem was.

About 6 or 7 weeks ago I heard there had been links to mood swings and depression from taking Singulair and immediately stopped taking it. It sounds cloche but it was as if the clouds parted and the sun began to shine again. I have become much more like my old happy and motivated self. My wife has noticed a huge difference as well as my friends and former coworkers. I am still having a little bit of a hard time staying on task but each day gets better and better. I sleep much better and the nightmares have stopped.

I think I'd rather deal with the allergy symptoms rather than take the FDA sanctioned poisons put out by firms like Merck. Their practices are criminally negligent but nothing will probably come of it because the regulatory agencies are in their pockets. It's all about the bottom line profits--public health be damned.

If any one is following what research is being done, here is the description of the new study in children.

http://clinicaltrials.gov/ct2/show/NCT00540839?intr=%22Montelukast%22&rank=19

Natto Kinase is an alternative to Warfarin and I am now using it. I have had stomach upset and gas with Warfarin and do not trust most doctors anymore. I went to five doctors with pain and swelling in my left lower leg, and shortness of breath. I put the diagnosis in their pockets. I stated: "I'm on estrogen, couldn't this be a DVT?" Oh no, this is normal we women age. The US Health Care system is nothing more than about money. It is money-driven, not care-driven. The ultrasound was cheaper than the idiots I went to. I do not plan on staying on Warfarin and am delighted the Japanese can offer an alternative!!

I see that the effects are finally hitting the medical community. There have been messages here from nurses, doctors and members of doctors families. Maybe now the word will get out. It's unfortunate that so many people have been forced to suffer while others lined their pockets. Worse yet is the ignorant disciples who expound the virtues of the new wonder drug while refusing to see the damage that is right in front of them.

On another note, my daughter just came down with the flu while at college. She went to the on-campus infirmary and while she was there she told them "no quinolones, my parents will not stand for that". She has seen the damage first hand at home. The doctor and nurse told her not to worry, they would not prescribe them at that facility because they were all to aware of the problems associated with these drugs. Thank god! Intelligent medical professionals do exist.

Concerning the class action suit....if anyone find info, count me in. I can't get my bicep back the way it was nor can I overcome these lingering effects (after 1.5 years) but I'd sure like to see they don't do this to anyone else..... ever again.