Vioxx symptoms and conditions

My 13 year old daughter was injured by Gardasil and completely disabled for the past year. Merck got it right when they used the slogan "One Less" for Gardasil. Because of Gardasil, my daughter was "One Less". She was "One Less Student", "One Less Active Child", "One Less in every aspect of her life". Take it from a mother who has spent the past year sitting by my child's bedside wondering if she would die in her sleep. INVESTIGATE BEFORE YOU VACCINATE. DO NOT trust your doctor to make this decision. If you want to understand Merck's role in the medical community, investigate some of their former wonderdrugs such as VIOXX and then marvel at how many people died from it before it was pulled off the market. The CDC AND FDA need to do their job and get this off the market before more children are harmed. The public is not aware of VAERS and the #'s are grossly understated. I have had to tell my child's doctors about VAERS and make them file reports or she would not be one of the current statistics in VAERS. Even then, her information has not been entered correctly so I know that VAERS is not what it should be. Please do not let this happen to your child.

My 9 year old daughter got her first shot in Dec. 2008 and her second in Feb. and the last in June. We have have been to the doctor a lot of times due to headaches with the doctor's opinion being that it's "allergies". She is now on allergy shots with still no relief from the headaches. I listened to her pediatrician and got her the shots. I feel so bad now after reading all the problems others are having with this vaccine. She also has had a change in her attitude aggression,moodiness,cries often, and she says she's depressed. If anybody has any suggestions for us please let me know. I love my little girl and know I'm worried.

This is to EZrust
Here are some facts. You obviously have no knowledge of anything medical whats so ever and if you do have medical knowledge shame on you for saying the things you said. Some of these side effect are not listed. And you say if it wasn't safe it wouldn't be on the market. WRONG!! Does any one remember VIOXX?? That was supposed to be safe and has since been pulled off the market. And what about all of the drugs that have recently been pulled from the market or are in the process of being pulled. This is similar to singular that has now been voluntarily dropped by some facilities because of the severe side effects that it had on children. Everyone thought they were crazy but when it was researched they found that the problems people were complaining about were TRUE!! Not all people react the same to medications. Some people have no side effects and some people have severe side effects. So before you go off on a subject make sure you know what you are talking about because you made yourself look very ignorant.

To ilovesummer: I'm glad that you may be one of the lucky people that have had no side-effects....yet. You need to go to the medalerts.org website & do a Basic Search, using HPV4 in the Vaccine field and also indicate "yes" beside the Died? field and you will find that 33 deaths have been connected to this vaccine - are these families just looking for something to complain about? If you are looking to the CDC, FDA or Merck for whether or not this vaccine is safe, you are looking in the wrong place honey. Money & politics are a big driver in the pharmaceutical industry; go to
****** and search "how the pharmaceutical industry educates doctors". I couldn't figure out why the Regional Health Officer & doctors in my area were pushing this vaccine so aggressively so I researched as many different angles that I could think of until I finally found it: in the last couple of years, Merck donated about $143 million to our biggest university - would you look a gift horse like this in the mouth, and endanger losing a donation like that?? Look up Vioxx, also brought to us by Merck, courtesy of the FDA, which ended up killing approx. 40K people, and surprise, internal e-mails are now coming to light (at trial) that show that Merck knew about the cardiovascular dangers of the drug all along, but gee, for some reason they didn't share that info with the FDA or the medical community. It seems they are very selective about the info that gets released about their drugs/vaccines...hmm I wonder why...

My 13 year old daughter had her third shot on 02/16/09. Her first two shots did not seem to be a problem. She said her arm hurt really badly after the shot, and the next day she complained of leg pains she hadn't had before. Within a few days, she had a high fever with body aches like the flu, except it wasn't the flu. She felt better, but a week later she still had a low grade fever. She was tested and had strep throat, and was treated with anti-biotics. A week later she started having stomach cramps and diarrhea. It's now March 18th and she still has diarrhea. I think it's criminal this vaccination is being given to our young women. How on earth could anyone think "possibly" preventing HPV and/or cervical cancer is worth the risk of what my daughter and so many others are having to go through?

Thank you for this site...although it is too late being I already poisoned myself with my 1st dosage - I know better now to STOP TAKING THIS DRUG IMMEDIATELY.
31 y/o male - non smoker - In good overall health.

What happened...(brief history of what got me to the point of being prescribed this horrid drug)
I caught a cold a few days after drinking quite heavily at a wedding (Aprox 1 month ago). It was severe enough for me to take a trip to this new doctor that is in my network and nearby (how I wish I could use my old family doctor that is out of network).
Symptoms then were congestion in my head and upper chest, cold sweats, runny nose. The doctor told me to take some over the counter stuff and try to fight it off w/ Mucinex, and Zyrtec - and lots of liquids. If that didn't work, he asked me to return.
It took about 5 days, and I seemed to kick the cold.
Approximately 2 weeks went by where I was feeling fine, then it seemed as if I was coming down with something again. (Last Thursday was when I started feeling ill)
I think what brought it on this time was breathing in excess dust at work opening some skids of paper in our warehouse.
Anyhow, this time around I had a pretty serious cough, felt feverish, and fatigued.
Sunday morning I woke up and took two Mucinex to break up the cough (which work great by the way)...and I hacked up something awful enough to call my doctors emergency line and have him paged. I was ready to go to the ER. It wasn't just phlegm or mucas - it was a soild mass of lord knows what containing blood. It look like an organ from a small critter.
Doctor said to keep taking the Mucinex and if I didn't feel better to come see him.
The coughing got worse on Monday, and the mucus I was spitting up wasn't pretty.
I went to see him yesterday afternoon (Tuesday) and he said its time to start you on an antibiotic and diagonsed me with an Upper Respiratory Infection.
He gave me Avelox, and Advair, and I asked for some of the good cough syrup w/ the codeine. He also sent me for a chest X-ray.
I got home around 4pm, made some food, then took some syrup and tried the advair.
I waited to take the Avelox til later on in the evening so I could set up a routine as I work nights and 9pm would be good.
I took the Avelox, around then, along with another dose of the cough syrup.
Around 1 hour later I felt extremely nauseous. I would burp, and feel almost ready to vomit...it was my body rejecting this horrible drug. The nausea came and went, came and went - then I got tired.

I laid down around 11pm and then the REAL trouble started. I must have fell asleep for about 30 mins, then woke up suddenly gasping for air...It felt like my heart was about to stop. I sat up in the bed panicked. I then got a little nervous, but calmed myself down, drank another glass of water and tried to fall back asleep. Sure enough just as I was about to drift off, the same sudden feeling of my breathing or heartbeat was interrupted and I sat up again. I had tingling in my chin area and in my arms. Walking to the bathroom I felt slightly disoriented and dizzy, and my legs and whole body felt weak. I also started getting itchy in my legs and groin area. Now I'm scared to go to sleep so I come to the computer and started researching this Avelox. It's 3:30 am now as I'm writing this. I looked at this site and http://www.fluoroquinolones.org/ before decided to post my experience.
I am still very itchy, slight nauseous, and feel disoriented. I'm scared to lay down to sleep now, but hopefully that will wear off soon - but I feel very nervous, uncontrollably. I almost want to induce vomiting to maybe get out any of the drug that is left in my stomach, but hate vomiting.
I will not take another dosage of this Avelox, no matter what this doctor tells me...and will give him a piece of my mind for prescribing this instead of something like ammoxocillin or just penicillin.

All I can say is:

1 – for no “explained reason” my neck collapsed and I needed a life saving fusion operation to prevent my spinal chord from going any farther into the brain. I was told that I “should” have died. I did not. It was less than one year from starting FOSAMAX. and I had no other symptoms that would have indicated the neck would collapse. Kind of like DEAD JAW, but in the neck.

Thankfully, vIOXX (which (allegedly…) prevents bones from healing (and spines – do a google on “vioxx bone healing”) was not on the market at the time… and the operation did fuse (else death).

Go forward one year… a later total lumbar operation, (also going to be added to a lawsuit in re to FOSAMAX) causing the collapse of the lumbar spine was needed. Sure, before FOSAMAX (allegedly) did its thing, it was supposed to be an EASY, ‘no sweat” operation that would merely help my body geometry a bit with a simple procedure - sure one more year of FOSAMAX and the spine was now about ten times worse than expected. The surgeon was stuned.

Anyway, that (total lumbar fusion) - failed because (allegedly) along to the market comes vIOXX…. I am pursing the detail, but as FOSAMAX is now known to give many DEAD JAW and it now appears that my neck bones destruct – which are near the jaw decided to destruct. Further, FOSAMAX is showing to have more problems than DEAD JAW. Had FOSAMAX and vIOXX not entered my life, I would have merely had arthritis and had done fine except for some pain. My brother, having exactly the same arthritis, DID NOT have either “poison pill”, and has done just fine, by the way.

2 - They are now finding that FOSAMAX also tends to provide problems with long bones and people are breaking femurs (allegedly) from FOSAMAX. Nice huh? So, now what happens? I simply fell and broke my femur – or I am now realizing that I broke my FEMUR THEN FELL – another thing people are finding out about (allegedly….). It also should not have happened as I DID NOT HAVE OSTEOPOROSIS and had fallen many times before I took the FOSOMAX POISON and it imbedded into my bones (takes about 6-12 months). FOSAMAX took me down big time, vIOXX kept me down. Almost having died 3-4 times from operations that failed and complications - I did not die obviously, and will continue my pursuit of the truth – look for a web site in a month or two…..

3 – So, FOSAMAX caused/contributed (allegedly again I must say….) the broken femur, and vIOXX stopped it from healing. That is called the “double whammy” in recent vernacular. After several operations (and over 6 months of hospitalization; 8 months total) failing without anyone knowing why or expecting that (my overall health was just fine except for arthritis and it was supposed to be a routine operation), they were about ready to amputate the leg. Fortunately, an astute NJ surgeon 150 miles away just realized IT WAS NOT GOING TO HEAL, and patched it together with glue, thus saving the leg and walking for first time in more than ½ year.

4 – I am going to leave alone the issue of “stress fractures” as this is enough to digest for now… but watch out for this issue….

5 – someone mentioned this: -- > “Can Fosamx D 70 mg be the cause of Ecchymosis Petechiae, I have developed what looks like an "under the skin" rash, on the ankles and upward on the leg, sometimes dark and also gets lighter…”

All I can say is that I went from having TEXTBOOK just beautiful circulation in my legs (was sincerely told it should be in a textbook) to a lot of problems, including very similar to the above AFTER taking FOSAMAX for 2 years. That was another quick thing to happen. Readers can interpret if FOSO may have caused that.

6 – I shall not forget, also, the horrible aches and pains I had within a few months of having FOSOMAX. I just thought it was arthritis acting up. NO, now I know it was from FOSAMAX. My whole history fits like a glove…

In fact, FOSAMAX brought me down, and vIOXX kept me down (allegedly). Merck should not sell their wares when they know their bone “science” was not “science” but a fraudeulent, dangerous and even (vIOXX) killing poison(s)…. (allegedly….)….

FOSOMAX and VIOXX were the very worst things to have entered my life. I pity others who had them concurrently. I shall spend 2009 finding others in the same situation with bone – spine problems from either or both concurrently.

If you have have had a bone/spine destruction or healing problem and taking FOSAMAX and/or vIOXX at the time – please feel free to email me at badbonehealing@hvc.rr.com. I will be creating a Web Site to dialogue and share research on. These (bone – spine) are horrible problems from these two poisonous (allegedly…) drugs and the PUBLIC NOW NEEDS TO KNOW. I asked the courts to help, and they have not. So, I cannot be blamed for not being transparent and doing as I said I would do.

Thank You…

bones
badbonehealing@hvc.rr.com

This article was published by the Wall Street Journal some time ago...but the point being if clinical studies of Mercks were questionable for want of a better word ..cheating..why would you go back to review old studies ...as surely now they are all suspect...............................................This week’s JAMA lands with one article that says some published studies of the drug were actually written by uncredited ghostwriters hired by the company, and a second piece arguing that Merck didn’t appropriately report mortality data from two studies of Vioxx in Alzheimer’s patients................................................

I have been reading all of these posts and have another question. I hope that someone can help. My daughter, 8 years old, has been on Singulair since she was 4. She is normally a very happy girl with a wonderful disposition. For the last year or so, she has been having trouble getting herself to sleep at night. She says that she hears things in her head such as ringing or "noises". A few hours before she knows it's bedtime, she cries and when we ask her why she's crying, she can't give us a reason. We initially thought that she was crying for no reason because she didn't want to go to sleep. I remember reading about the side effects of Singulair causing mood swings, etc., but her's are not violent mood swings. Just very emotional and has a hard time coming down from the "episode". I'm at a loss...I have not talked to her doctor yet about it, but have told her that we will make an appointment this week to discuss it with him. My husband suggested that maybe it sounded like she was having a panic attack or anxiety attack. I hate to label her as that at such a young age. My mind now goes back to the side effects of Singulair and maybe this is to blame. Any help or suggestions would be greatly appreciated. Thank you! Concerned Mom

I have been reading research reports that show that montelukast (Singulair) has a higher pKa than many of the other quinoline malaria drugs. That means that Singulair ionizes more easily than even drugs that are known to cause terrible dreams, hallucinations, depression, anxiety, and suicidal thoughts. Many researchers believed that the problem with Vioxx was that it ionized under certain physiological conditions.

I will report again when I can confirm the numbers. I am not sure if it is confirmed that montelukast's pKa is around 5.8 and the malaria drugs is around 4.8. I need to do more work before I can point out that it is not impossible to theorize that montelukast ionizes like Vioxx.

My 54-year-old fit, social, successful husband was put on Singulair in January for newly diagnosed asthma. He developed a depression with anxiety, irrational fears, avoidance, mood swings and even one episode of suicidal thoughts out of nowhere. He saw a psychiatrist and a therapist, tried medications, yoga, a vacation, meditation, breathing exercises - everything! But he kept getting worse.

The day he was throwing patio furniture then sobbing uncontrollably was the day he realized he couldn't work in his condition. He negotiated a 60-day leave without pay. Even that didn't help. It was crazy. How could a man who managed hundreds of employees and a major health service system for 20 years suddenly be so paralyzed with fear that he couldn't walk down a beach or go into a Walgreen’s?

We found this site May 26th. He stopped the Singulair immediately. It has been 10 days and he is already 80-90% back to normal. Thank God.

Partly I am writing because it is so hard to read of parents' guilt that they "should have known" etc. Look, unlike a child, my husband is mature and very verbal; he is also a psychiatrist (!) with a capacity for self-examination and a language to describe his inner experience. And me, I'm a psychologist (!) trained in understanding people and I know him very well. And yet with all that training and skill and consultation and treatment, WE STILL COULDN’T FIGURE THIS OUT! So please, don't make yourself feel any worse with guilt. This is awful and tragic enough already.

I would add that the onset of mood and behavioral problems is so insidious that it is hard to connect the problems to the Singulair. Also, I suspect that children and adolescents are at greater risk because of their immature emotional developmental level. An adult l suspect may need some genetic or personal predisposition to mood disturbance, or stress, or both, to trigger these side effects. My husband had a depression episode 30 years ago and had recent traumas that certainly could have triggered the depression. But how treatment resistant that depression was, and those strange paralyzing fears and extreme anxiety – all that I blame squarely on the Singulair.

I have made a report to the FDA. I urge you to do the same.

I am posting an email address for people that have stopped dispensing this drug and see the symptoms of the side effects disappear.Please tell all who have seen a change in their child or loved one to email this woman.I met with Dr.Sarah Sellers and other members from the FDA in Washington DC she is in charge of Safety Review in the office of Surveillance and Epidemiology.This is critical in the investigation into SINGULAIR .Everyone wants to help and this is how to begin.The email is sarah.sellers@fda.hhs.gov Our Congresswoman has requested the TV advertisement for SINGULAIR to be changed,they are stating mild side effects and that is not known to be true at this time.I am reaching out to all of you who have posted and that know anyone who has ,to please do this along with filing on ******.We have to work within the guidelines of the system,this will certainly help the investigation to be more accurate.My husband and I are in this to help all the families that have suffered so greatly,take this opportunity to help also.Thank You in advance Kate and David M.

Hi, I am a mother of 6. They are 11,9,7,4,and twins 2 1/2. So nothing surprises me as far as kids. I have been through it all. My 7 year old had been taking singulair for allergies and ear pain, for over a year. Did my doctor once ask me about any of the side effect, NO!! This is not ok. My son suffered, decrease appetite, weakness, fatigue, mood swings, irritability, fears of being alone, scary dreams, anger, bone and joint pains. Before he was a loving kid (who had his moments)!!! I had no idea the singulair was causing all these destructive side effects. I just thought this is a phase he is going through, he will soon get over it. Finally I took him to his ped. and we did blood work and x rays. I told her something was wrong with him, he has not been himself over the past 6-8 months. This is one reason why I never suspected his singulair, it did not show up immediately. All of his test came back fine. I just happened to look at the side effects of this medicine. I almost died!!! Every single thing that this poor child has suffered from was on this list. Then more, I found this page and other mothers have had the same experience. I was just amazed that this has happened to so many. I was relieved that my son was normal. He has been off singulair for 6 days now (he doesn't know why I took him off it) . But you would not believe the change. It is AMAZING!!! In only 3 days, I started to see change in his anger. You would not ever in a life time believe that a medication can do this. I have been poisoning my son for a year. I think that Merck should take some of that 4.3 BILLION dollars and do some better research!!!! Concerned citizen you are right on. I have read many pages of this forum and I think you are doing a good job researching this. Maybe Merck should hire you as one of there "experienced personal". It just makes me seriously sick to see that the medical field is not seeing this problem!!!

I just saw this post and it makes me feel ashamed of our medical system which includes everybody.

about 12 hours ago on Apr 14, 2008 by jerseymomma, #7220
My boss has been in contact with all of the top law firms in the NJ & PA area. We want to make sure that we give you info thats actually going to help and not send you to some bloodsucker. When you file an injury suit, there is no money out of pocket. The lawyers only get paid if you win your trial or the case settles (so if you loose-- u dont loose anything either). And as a heads up, if this is something that can be proven to a jury, the suits take fooorrrrever. I think that is the worst part for the families that I personally have dealt with regarding liability suits-- u want closure and you want answers but it takes so long to get them!

Let talks about the "everybody knows category" of the pharmaceutical industry.

1. Everybody knows that: There are many compounds that never go to market for various reasons. Even back then, no pharmaceutical company wanted to spend money on a drug that was not as chemically "reliable" (I chose that word to encompass many things) as possible in all of the known interactions that could be expected in clinical use. The categories are also "everybody knows."
2. Everybody knows that: Merck did a lot of testing for "reliability" on Singulair. But Merck also did a lot of testing on Vioxx. No conclusions can be drawn from this per se.
3. Everybody knows that: Even back then, important decisions were being made as to whether to market a drug that related to how body enzymes metabolized that drug (meaning utilize the drug and then break it down so that the body could eliminate the waste products.) Genetics differences between different people were a factor that were also put into the decision making process.
4. Everybody knows that: clinical variations in efficacy and side effects can be a result of different factors. Some might include 1. genetic differences 2. drug-drug interactions 3. improper use 4. diet - take the grapefruit juice example. Those are just some.

What we don't seem to do in this country is adequately monitor post marketing complaints? Why did it take five years to find out about Vioxx? If we did monitor more carefully, could we identify some thing that was overlooked or the technology has changed so that it is easier to identify what is wrong?

When there is a problem, there is no way that we should go back to the same company for an explanation of the problem. Everybody knows that many companies work on the same category of drugs. Sometimes those companies encountered some road blocks and they abandoned the drug category. The FDA ought to require everything from everybody to get to the bottom of the problem. And also hire independent evaluators.

The next part of what I have to say is just a hypothetical - a FICTION like a WHAT IF. This is just to make a point. What if another group got different results for the metabolism studies? What if another group decided that the drug was not reliable because a hydrogen bond at a certain location could be influenced by too many different factors to be able to accurately predict what would happen?

So why do people have to hire lawyers, when the FDA should be doing it's job? There are many specialities of law just like the doctors. Does getting to the bottom of this problem require the lawyer-chemists? Why is it their job?

I am repeating one of my post regarding the Swedish study of the side effects of Singulair. When I read that parents have complained to their doctors about side effects and been dismissed, and told to continue the medication, I truly questions whether these doctors are giving their patients the right to INFORMED CONSENT.

I have been told by doctors before something like this "That is my professional opinion - I stand by it ." And I have said right back-- I understand that is your opinion. But if you don't have the time to tell me what I need to know then I am not giving you my informed consent. I get an entirely different attitude after that point. Because, that is how doctors get sued. Parents/patients didn't understand.

1. Have parents been told the complete reasons why it would be absolutely necessary, just necessary, or desirable to take Singulair and why?
2. Have parents been told what the alternative treatments are and the possible side effects of those treatments?
3. Have parents been given an option of another treatment when they complaint about the side effects of Singulair?
4. Do parents know that headache is a side effect that occurs in 18% of patients? These headache have indicated some serious events in European hospital reports. They are not just sinus headaches.
5. Do parents know that Singulair can cause serious events that require hospitalization as referenced in European hospital reports? These reports have described the event and provided laboratory test results that prove that Singulair was the cause.
6. Singulair in NOT an anti-histamine. Can your doctor fully explain to you how Singulair interacts with the receptors on the mast cell (cell part of the immune system)? Can your doctor fully explain how the mast cell will be changed by this? The mast cell has a number of receptors that interact with each other to tell the mast cell how to function normally; when it's time to die; when it's time to be replaced; and when to tell the bone marrow to send a replacement mast cell. Singular CHANGES the immune system---- good or bad???

So here is the report from Sweden to take to your doctors. Would your doctor give consent for his/her children after reading this? Maybe he/she would BUT at the very least that doctor would be looking for side effects that could mean trouble.

------------------------------------------------------------------------------

Update: I have spent hours searching scientific data bases for articles on Singulair. So far this is the most direct reference to adverse drug reactions and Singular.

For anyone who wanted to print the article from the Swedish researchers that stated that their study suggested that montelukast (singulair) should be investigated for adverse psychiatric drug reactions, I was able to find a link with open access to the public. So far, this is the only article that I have found. I am still searching through databases. This link should work if you cut and past. I am sure that all doctors would appreciate the opportunity to read it for themselves to see what they think.

PRINT REPORT.

http://www.biomedcentral.com/1472-6904/8/1

Individual case safety reports in children in commonly used drug groups – signal detection Gertrud Brunlöf , Carina Tukukino and Susanna M Wallerstedt Department of Clinical Pharmacology and Regional Pharmacovigilance Centre, Sahlgrenska University Hospital, SE-413 45 Göteborg, Sweden author email corresponding author email BMC Clinical Pharmacology 2008, 8:1doi:10.1186/1472-6904-8-1 Conclusion In conclusion, the present study indicates that ADRs are reported for commonly used drugs in children. The number of ICSRs varies in different groups of drugs. A possible signal for montelukast and psychiatric adverse drug reactions was found, which should be further explored.

Please don't forget to PRINT the Tables which open on a separate page. Table 2 lists the specific side effects that they found which include anxiety, aggression, night mares, pain, and several others.

This is the beginning of day four with no Singulair. I can still breathe, but I switched from one puff of Advair per day to two. I decided to look Advair up as well and was dismayed to find similar negative experiences with THAT drug. Hopefully for me eliminating one is enough, because I know that I need something to be able to breathe. So far yesterday was the best day emotionally, I felt a sense of calm several times throughout the day, and didn't need to be occupied with busywork to distract myself from my own thoughts. I don't have stomach pains anymore, which like most of the other symptoms I never attributed to Singulair, my head and heart just feel much "lighter" if that makes any sense. I don't feel sad, or anxious, or suicidal. I feel like I have some focus back, not completely, but a lot more than last week! I also feel like I am better equipped to handle upsetting information instead of feeling overwhelmingly sad about everything. I had my boyfriend read some of these posts yesterday, because he has been trying to accomodate my behavior for a while now, and he pointed out not only some of the obvious side effects, but there was a post about hand and joint pain, and I was constantly asking him rub my hands. I hope that sharing will help others if they are feeling anything similar, and if it's possible to stop Singulair and still breathe okay that they should try it. It is a synthetic chemical and none of us really know exactly what the short-term and long-term effects of any of these medications really are. I mean, Thalidomide was great for pregnant women who suffered from morning sickness in the '50's. Vioxx I'm sure helped many people with painful arthritis. It's only later do we find out the negatives to taking these drugs. I hate that illegal drugs are so very frowned upon in this society but "medicine" from your "doctor"is okay. Doctors nowadays I think are overwhelmed with their caseload and they read the same pamphlets that are handled out to us, laypeople, and recommend these pills to us. Drug company representatives spend a trememdous amount of money on free lunches and mugs and mouse pads and of course, if it's passed by the FDA it must be a-ok! so why not? Many patients come in ASKING for a particular drug because it is advertised on TV!!! Hard alcohol and cigarette commercials are banned, right? So how it is ok to peddle pills to us? I so many times wanted to ask my doctor about Lunesta because I couldn't sleep, and Cymbalta because "depression hurts everywhere AND everyone" and I was in so much psychological and physical pain but something told me that I didn't want to keep adding to the list, I wanted to be healthy enough someday to take some medications away! So I suffered with insomnia and debilitating depression hoping someday I could get better on my own. I wonder how many other people out there on medications who have complete faith in our healthcare system are doing more harm to themselves than good?

As a pediatrician I write for singulair every day.
The medication is for allergies.
Allergies cause adenoidal swelling, which cause sleep disturbances which makes the child tired the next day with makes him over weight, less attentive, hyper and eventually act out.
This in turn makes the child experience parental, peers and teachers criticism/ abuse, with leads to the child feel inadequate, embarrassed, frustrated and eventually depressed and suicidal.

Yes, singulair does cause behavioral change but they appear within the first couple of peels, the rest is due to allergies, lack of medical care, i.e. sleep, singulair, and zyrtec deficiency.
Allergy shots cause 4 times the incidence of suicidally than singulair, and Ritalin 10 times more.
They say in hebrew "once a stone is thrown into a well, thousands of smart people won't find it".
Check it, it's true.

Wow, i just happened to see on the news that singuilar has these side effects. As i write this i can't stop from crying. My 8 year old son has been on sigular for a year and a half now. He has had fits if rage, feelings of wanting to die, leg pain, stomacher pain, almost every symptom others have had. I would stay up crying at night trying to figure out what was wrong with him or me as a parent. Shame on the doctors who should of known better. I went to his doctors and told them about his behavior and outburst and physical complaints. I was told it;s a phase he going through. My son would tell me his legs hurt when he walked, well i thought it was gowning pains like the doctors said. I am so glad i found this web page. I now know for sure it is the medication. I will now search for a better way to treat his asthma and allergy's. I hope and pray that others will find this web page and know there isn't anything wrong with us or our children, however there is certainly something wrong with our doctors who should of seen the symptoms and told us what it could of been.

I was put on Toprol XL 6.5 yrs ago. My heart rate had soared to 130+ and b.p. was elevated. So my family doctor put me on Toprol XL 100 mgs. From day one I felt exhausted. He told me that would soon clear up and not to worry, we needed to be more concerned with my heart rate and b.p. I listened and was a good patient. After a year of total exhaustion and having to quit my job I asked to be taken off Toprol. He said it was the only medication that would control my heart rate and b.p. together. He agreed to reduce it to 75 mgs. After a few months I went back and said it was still too much! My b.p. was better as was my heart rate so he lowered it to 50 mgs. Things got a little better at least I could get out of bed by 10:00! Fed up I lowered it to 25 mgs. and tracked my b.p. Finally I told my doctor and he said as long as my b.p.was better 25 mgs.was ok. By this time though I was having other symptoms, body aches, joint pain, mind fog. He attributed it to arthritis and put me on Vioxx. 2 pills later I stopped due to chest pains. The symptoms I had experienced over the past 2 yrs continued so I sought a new physician. Once again he said Toprol XL was the only medication I could take for tachycardia and high b.p. My b.p. was again elevated so my meds were increased to 50 mgs. he wanted to go 100mgs., I said NO!
In 2004 I was diagnosed with Fibromyalgia, the pain had become so bad now it was debilitating. I had all the full blown symptoms of Fibro, extreme exhaustion, body aches, joint pain, mind fog, depression etc etc. So I sought treatment for Fibromyalgia for 3 yrs. Not so successfully I might add.
I should note that I had none of these symptoms before Toprol XL.

During a recent Gynecology visit my b.p. was extremely high. I told her my story about Toprol. She said point blank, They are NOT listening to you. I think all the side effects you have been having are due to the Toprol XL.She sent me to a Cardiologist. God bless her!!
After many tests he immediately took me off Toprol. He put me on another medication instead. I am having withdrawal side effects from Toprol, shakiness, shortness of breath, heart rate acceleration and mind fogginess. But, anything is better than another day on Toprol. He told me what I was experiencing was normal withdrawing from Toprol. He also assured me there were many other alternatives to Toprol and if the new medication doesn't work there are other options.
I think Toprol XL is the next drug that should be banned!! I pray everyday my life will return to what it was before Toprol XL and that I will not have any lasting side effects from this horrible drug.

After reading the many complaints about the side effects of this drug, I want to know what we can do to get this drug taken off the market. Each time, I've mentioned to my doctor about this medication causing me to be extremely fatigued, she quickly dismissed my complaint. Many doctors are not listening to their patients. I wonder just how many of them are taking this stuff. What is the first legal step toward having this medication properly investigated???

I lterally just starting taking Yasmin today. I used to take Tri-phasil, but found it just wasn't keeping my mood in check over the last 6 months, not to mention I was suddenly getting 2 periods a month. So, I stopped taking the pill for a month, and after seeiong ads for YAZ ended up with Yasmine after visiting my Dr.
My questions for the ladies with symptoms of anxiety and mood swings: Did you not have these symptoms before starting the pill? If so, are you saying that Yasmin made them worse?
Also, I would be curious to find lout what BC pills you NOW use, and how the hormone dose compares to Yasmin. The Tri-phasil I used to take was stronger than Yasmin. If I begin to feel any side effects using Yasmin, I will have to assume that I just need something stronger and will begin with Tri Phasil again.

38y.o F taking toprol 100mg once a day for hypertension x 15mths History of Hypothyroidism which is controlled w/ synthroid and closley monitored w/ lab work.
Experience weight gain, unable to lose weight w/ diet and exercise including w/ a nutrionist and personal trainer. Hairloss, lack of libido, chronic joint pain, swelling in hands and ankles/feet, back pain and/or muscle aches, lack of interest in everything, no energy. Major swelling after high sodium intake. Ear drainage, tingling of extremities especially in feet and fingers, visual disturbances. Blood Pressure is okay.
Has anyone experienced an improvement since they've stopped using toprol?

Update on ring removal...I took my ring out July 13 after reading everyones side effects on here and realizing the horrible way I'd been feeling was because of the ring. The first week after it was out was not so pleasant my period started the next day with horrible cramping, it only lasted 2 days though and was totally worth it. The mood swings and irratability lasted for about a week after it was out and was pretty severe. After getting past that though Ive felt fantastic, my energy is back, Im sleeping through the night, no more discharge, not a single headache in 3 weeks. The biggest change though has been my mood, I feel like my old self again, no more crying and psycho irrational thoughts. I will NEVER use the NR again, looking back on the whole expeirence I felt like I was poisoned by it mentally and physically. I urge everyone to tell any women you know about this site if they are on NR, it really pisses me off this BC is being marketed as "safe", from my own experience and others Ive read about it's anything but. If you look at all the law suits being filed against NR, and past meds like vioxx, phen phen, and the countless others that are marketed as "safe" and approved by the FDA, it is apparent that "safe" is used loosely in an attempt to generate profits and dollars, even if it means putting peoples lives and in NR's case also mental health in jeapordy. You should decide for yourself of course if your going to quit using NR but from my own experience taking it out was the best thing Ive ever done for my own health and safety.