Pharmaceutical company symptoms and conditions

The medical professional is particularly unhelpful in this matter. Talking with medical personnel about fluoroquinolone poisoning is a go-nowhere exercise. In an era when Monsanto genetically-modifies our seed stock you might think medical caregivers would advise us in advance that their prescription antibiotics mess around with their patients' DNA. (IT's that deregulation thing, yes?)

I experienced painful calves and a strange dream, possibly a nightmare, immediately, e.g., on the very same night, after having injested one Levaquin dosage for a prostate condition and maybe a year after separately having taken cipro for a week to combat traveler's diarrhea. The post-Levaquin early evening dream was strange insofar as I rarely drempt, and I never recall having been roused to wakefulness by a dream shortly after having gone to bed. Early on I did NOT associate Levaquin with the really terrible symptoms that I experienced within 60 days of having injested Levaquin.

My wheels fell off when I entered a period of insomnia. I thought my sleeplessness was stress-related because my health history includes a major depressive episode 11 years ago. I presented myself for help to a psychiatrist who prescribed a small dose of an atypical antipsychotic as a sleeping aid. My drug-induced sleep felt like a coma that lasted each night for a couple of hours. There were heart palpitations, agitation, panic attacks, racing heart, racing thoughts, insomnia, depression, paranoia, poor cognition, body shuddering, muscle twitching, night sweats, and pain in both Achilles heals. The symptoms filled a note book page. I felt like Jean D'Arc who was being burned chemically at the stake from the inside out. I would rise in the morning and then minutes later fall back into bed. I could stare off into space and completely lose track of time. I could not even find the right words in mid-sentence. I could not fill-in the registration papers when I presented myself for a second opinion at Mayo Clinic. I became a full babbling idiot. My wife said that I had retreated or devolved into some kind of primate or ape who communicated solely his emotional states by means of eye contact only.

I asked my doctors if the sum of levaquin and cipro had pushed me over my peak quinolone tolerance level. Or was it the medicine that the psychiatrist had prescribed to make me sleep? . I was no stranger to depression and I knew my symptoms were not merely emotional or psychological in nature. Why did I always feel as if I had been poisoned? The psychiatrist decided my paranoia warranted higher med levels. I declined the advice and stopped taking the meds altogether. My anxiety today is lower, my sleep is improved but fitfull. My neck aches. My head feels as if it were in a vise. It's not a headache and it's not painful, but there is a tingling, crawling, scorching sensation at my forehead and behind my eyes as if someone had beat me with a pillow and then filled my head with novocaine.

I'm not sure there's a moral to the story. It might sound a tad over-the-top, but I think we're faced by a pharmaceutical plague. There's really no excuse for the absence of informed consent. There is nowhere above ground, e.g., nowhere on main street, and no-one with whom you can speak in order to take the full measure of fluoroquinolone poisoning. If you are at this URL merely to find out about the FDA's recent black box warning re: Levaquin's link to ruptured tendons, you are in for peep into hell. Read the other thousands of postings on this site, and decide for yourself who bears the ring of truth.

I am a male 55. Started taking Altace 15 years ago. BP kept creeping up. I work outside for a living. Sometimes work is very hard, climbing mountains, carrying land surveying equipment ect. Dr started me on lisinopril 40 mg, dropped altace which I had been taking with HCT 25mg. Started getting numbness in left hand and charley horse in elbow after playing mandolin for 10 minutes. I thought this strange. Now I have muscle cramps in legs and I am wiped out when I get home. (thought must be getting old) Then other joints, shoulders, and knees stared hurting and lower back. Started thinking what has happen to me?! I am completely falling apart! That's how I found this web site. Now I wonder, snake venom sounds about right. I had started thinking I had been poisoned. Guess I'll make a DR appointment or move to an "old folks home". At least I won't have a stroke.......right?

Hi All,

I was diagnosed with dermatologists when I was 14 years old and put on very high dosage of prednisone to get my disease under control (40 mg a day at the beginning). My muscle enzymes were out of control (CPK was almost 8,500 when it should be less than 215) and I was barely mobile, huge amounts of weight loss, alopecia, Raynaud's, etc. That was 11 years ago and I am now almost 100% better. Prednisone saved my life, but the side-effects were TERRIBLE! Especially for a girl going through puberty. Kids at school don't understand you're sick, and they can be extremely cruel. Luckily for me a large number of my family members are in the medical profession all over the world and my parents were able to pool knowledge to find the best treatment for me without all the horrible side effects. An uncle in Germany suggested I take a Prednisone alternative widely available in Europe called Diflazacort. This medicine is not available in the states apparently because the FDA thought it was exactly like Prednisone so was unnecessary. I'm sure this is some pharmaceutical company lobbying to preserve Prednisone's monopoly on inflammatory diseases, but regardless it makes finding Diflazacort difficult for Americans. This is a HUGE shame since this medicine gave me ALL of the benefits of Prednisone with NONE of the side effects. My mood swings, water retention, increased appetite, hazy brain, thinning skin, etc etc etc ALL stopped with Diflazacort. This wasn't only true for me either. A family friend had been diagnosed with Crohn's at the time and he was put on Diflazacort from the beginning of his treatment after seeing how I reacted to it and NEVER had any of the negative side effects I had to deal with. Really this drug was like a miracle for me. Prednisone prevented my sure death, but Diflazacort gave me my life back in its entirety. I've now been off of any steroid for 7 years and my muscles are fully back to normal. Some of the fat deposits Predinose caused still linger, but to most people's eyes I'm totally back to normal. I wish I could find everyone having problems with Prednisone side-effects and tell them about Diflazacort. Even though it isn't available in the states (although I heard recently they are trying to get it approved again since a number of studies showed Diflazacort is much more effective treating Crohn's than Prednisone is) you can get it on the internet or if you have doctor friends abroad as I did. I'm always wary of buying drugs over the internet since there's no control so I would suggest contacting doctors in Europe or Asia directly or through your doctor here in the states. Anyways, I wanted everyone to know that some people do get better and I wish you all the best of luck!

Hi All,

I was diagnosed with dermatologists when I was 14 years old and put on very high dosage of prednisone to get my disease under control (40 mg a day at the beginning). My muscle enzymes were out of control (CPK was almost 8,500 when it should be s no control so I would suggest contacting doctors in Europe or Asia directly or through your doctor here in the states. Anyways, I wanted everyone to know that some people do get better and I wish you all the best of luck!

I already had my side effects written here and I wanna thank to the person that started this web-site.
AND
If anyone decides that there is something we can do against the pharmaceutical company that is keep making this pill - let me know because I'M IN!!!!!
Let's see if we can stop this one way or another.
Yasmin is on of the most prescribed birth control pills. In Europe, 14 GIRLS DIED BECAUSE OF YASMIN, one last week, a 22 years old from Croatia. Imagine how many others could have died and no one knows the reason!

Hi Ladies- I promised I would post to let you know how I am doing WITHOUT Aviene. I posted the Sept. 10 comment entitled Thanks ladies because I felt your posts have helped me.

I stopped taking the Aviene on a Thursday and all side effects stopped and no new ones occurred. All is well, I enjoy life without being a freak show.

In a DAY AND A HALF WITHOUT AVIANE MY HEALTH RESTORED.

I mentioned the 20 pound weight gain within a few weeks, by the following Tuesday I lost 9 pounds and today is the 26th and I lost 15 pounds. No anxiety, no irritation, no face issues (in a week it cleared up), no mood or energy issues, no excessive thirst, burning of eyes, chills, fever, rashes, itchy -nothing. I was allergic to it and my body wasn't breaking down the coloring agents etc whatever the hell is in there b/c it's not like you get a box or product descriptions. This isn't personal comments, I spoke with pharmacists, doctors, doctor friends, nurses etc. I work at a hospital I have great resources to share with you.

Whatever your side effects are, let's do this. Let's listen to our bodies, listen to experiences and draw your own conclusions.

I know my body, I know myself, and I know my life changes, mood changes, physical changes were due to this pill.

Please consider when being worried about what will happen if you quickly go off it that the consequences of staying on it are more severe. For me, and for many of us, the side effects didn't stop but kept adding and if you are reading this and are just curious or feel something is off with you do not take it any further. I am sharing that I am not a sensitive person and do not experience side effects... and I completely broke down physically and mentally from the amount of side effects and had to self defend.

Many of your comments helped and let's face it if you read that some ladies lost their hair... come on... obviously something is wrong with this pill.

Take care ladies, my sincere hope is that my post will help you, as you have helped me.

So you know, I went back on Alesse and all is well. My drug company didn't cover Alesse but ALESSE HAS A PATIENT CARD FOR THOSE WHO DO NOT HAVE INSURANCE AND FOR THOSE WHO DO BUT THE COMPANY DOESN'T COVER ALESSE RATHER THE GENERIC AVIANE. Your patient Alesse card you get will cover the difference that your insurance company may not. I paid $ 2.89 for my monthly prescription which is less than if the insurance company covered it. Check with your pharmacy location site if they participate in the program and it is not hard to find one that does.

You may not like Alesse, I can only share my experience with Aviane that did make my life a living hell. Happy to be OFF it!

Please take care and self defend your situation and reach out to those around you.

My 6 y/o daughter has been taking Singular for approx. 2 years. She began to have regular stomach pains shortly there after. She was sent to Children's hospital where they put her on a laxitive which made things worse. Then we began testing for food allergies only to find out that she tested positive for a 3 page list of foods. We eliminated those food and had her tested again. She was subsequently allergic to the foods we eliminated. She was recently down to rice, a few meats and some vegetables. Guess what, she is now allergic to those foods.

All this time she has been complaining of severe leg pain, eye pain, throat pain, numbness and tingling in her hands a feet, all of which come an go. I have reported this to all the doctors and specialists we have seen. She had undergone countless blood tests to rule out autoimmune disorders and all come up negative.

She began to develop severe anxiety and just had the blues most of the time. She would be crying and saying off the wall things like, "I don't think my fish is happy". She couldn't stand to be away from me and would stress out about even weather or not she would sit by me at a restaurant. I mentioned this to all of the doctors. They said to not make too much of it. One suggested she see a psychologist. NOT ONE DOCTOR EVER LOOKED AT THE SINGULAR.

Finally about 4 weeks ago my neighbor who is a scientist at a pharmaceutical company called me and told me about the "black box" warning that had just come out on Singular. I took both of my children off of it immediately. My daughter went through about a 10 day period where her anxiety got worse and then it was just gone. We are adding foods back into her diet and at this point she has not had any severe allergic reactions.

The last 2 years have been a complete nightmare for her and for us. I am a medical professional and I have had doctors treat me like a hypocondriac, hypersensitive, attention seeking mother. I feel so justified and saddened by the recent findings all at the same time. Most of all I am so grateful that we figured this out before things go even worse.

Please let me know if anyone else is suffering food related reactions as a side effect.

Just had mine inserted..it wasn't a pleasant experience at all as my cervix kept tightening up. I didn't feel well the rest of the day, cramping, bleeding, and fatigue. Better today. I hope I don't develop further problems/
What surprises me about this site is that many of the things you are describing are listed by the pharmaceutical company and the FDA as warnings and precautions as well as possible side effects. My doctor went through all of these step by step with me. I have a follow up appointment in 4 weeks and then another at 12 weeks then annually...all to check the device.
Yes, it is terrible that you had to go through these things, but this is a foreign device that is inserted in your body to deliver progesterone...if you are breast feeding, this will get to your infant; you are at risk for an infection; you are at risk for it to move/dislodge; it is a hormone and you may have adverse effects; it shouldn't be used if you have fibroids; immediate postpartum use is cautioned.
I am glad you are sharing your experiences, but I think it would be even more useful to report them to the FDA. Thanks.

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

Please contact me if you would like to help by sharing your story with the media,I am looking for stories of recovery after stopping the medication.Please use my private email under kate2 or just reply under this posting.Kate M.

I am a 47year old male.I,ve been on simvastatin for about 10 weeks now and have been experiencing mild short term memory loss for a few weeks. I put this down to the onset of old age?. I,ve also been getting spurious pains to elbow and finger joints? could these problems be associated with the medication?.

In my previous message I was wondering why the same medication has to have so many different names.

I haven´t had a reply to that, but I found some information on Wikipedia that migth be helpful when looking for more information.

Zocor (=Simvastatin) can have many different names as you can see below.

"Brand names: Zocor, Zocor Heart Pro, marketed by the pharmaceutical company Merck & Co. and Denan (Germany), Liponorm, Sinvacor, Sivastin (Italy), Lipovas (Japan), Lodales (France), Zocord (Austria and Sweden), Zimstat, Simvahexal (Australia), Lipex (Australia and New Zealand), Simvastatin-Teva, Simvacor, Simvaxon, Simovil (Israel), Simvotin (India) and other."

I don't think that anyone can predict a time frame for getting over an adverse drug reaction. Below is my opinion but I see a lot of evidence that it is basically shared by other people maybe not exactly as I state it.

Adverse drug reactions deplete many essential nutrients from our systems. Inflammatory response is very stressful on the body. It is sometimes a very big effort to work on the diet to put back what has been taken away. It can take a long time.

Quinolines particularly deplete B-vitamins, folic acid (B-9), calcium/magnesium/zinc and omega-3 fatty acid. Sometimes the blood-lab work shows elevated homocysteine which proves that the body has suffered inflammation. Cardiologists now use homocysteine levels to show whether someone is at risk for heart disease due to inflammation. Deficiencies of B-6, B-9, and B-12 are known to cause elevated homocysteine.

Here is the pharmaceutical company ZINGER. Now companies such as Merck and Pfizer are going to offer niacin products to lower cholesterol. Well, yeh, duh !. All of these drug reactions are causing depleted B vitamins which elevate cholesterol. Then after they have tried to kill us by depleting our B - vitamins, they want to sell us another pill to give the B vitamins back to us. How many people out there are on some kind of a pill with side effects that cause inflammation? What a business? It is win, win, win.

In September of 2007 my then 13 year old daughter was put on Singular for mild asthma. At the time she was a straight A student, vice president of our school and a popular girl who's guidance counselor described as "the glue of her grade" because she was so well liked. In November she told me that she was struggling with advanced Latin and Science. She asked to drop down to on grade Latin so we did. In December her science teacher notified us that she had a C average. She told me that she thought she had ADD/ADHD and she couldn't keep up. At the same time she was having a lot of problems with friends at school and we just attributed it to being 14. 3 weeks ago we discovered that she is significantly behind in English and it was then that she told me that she is been having horrific night mares. She said that they usually involve someone killing her or her killing herself. She said that they were so graphic that she couldn't repeat it out loud. She also said that she would feel waves of anxiety that would come over her at school and she would act "witchy" to the kids in her class for no real reason. She said that sometimes when she is trying to do her homework she will read the same passage for 2 hours and still have no idea what it's about. She also said that the suicidal thoughts from her sleep happened during they day and that she had thoughts of her harming herself. Fortunately her pulminologist told us that this may be caused by singular and we immediately took her off of it which was 2 weeks ago. She has only had 1 "bad dream" not even a nightmare since. She had one anxiety attack 3 days after she was off it and she describes her moods as the "cloud lifting....slowly". Now, we have to pick up the pieces. Her grades have suffered, her friendships have suffered and most of all her self esteem is very low. I'm grateful that we found out the cause but I feel as if my daughter lost a year of her life and I worry that because Merck won't admit there are side effects we can't find out how long it remains in their system. Is anyone else concerned about the long term affect and has anyone pursued a class action suit to try to get this drug tested properly?

I am posting this as a new post. I am not against Singulair. I am against withholding negative side effects from the patients. I am against promoting that Singulair is safe and effective for everybody on the planet.

My entire family is health care. My father was a surgeon. I worked for a pharmaceutical company. Pharmaceutical companies are supposed to ethically invent drugs and inform everybody about the safe and effective way to use those drugs. Pharmacists are supposed to police the prescriptions and dispense the correct dosage. Then pharmacists are supposed to be aware of side effects and drugs interactions. When necessary, pharmacist are supposed to intervene to prevent a mis- communication from turning into a disaster. Doctors are supposed to review the recommendations of pharmaceutical companies (who are policed by the FDA) in order to determine if their diagnosis matches the profile of drugs known to be therapies for certain symptoms. I, personally, am madder than hell at Merck. Singulair could really be a good therapy when it is needed. It could correct some bad stuff that happens short term. Why does Merck's need to make every drug a major block buster money maker ruin the market for Singulair?

Wow what it is with all these doctors not knowing these side effects, don't they know that there butts are hanging in the wind,the law protects the drug companies ,but doctors you are not immune

I am a hill walker. My name is Steve and I am 58 years old. I have been recently diagnosed as having type 2 diabetes. Fair enough. I have been given dispersible aspirin, metformin to lower blood sugars, ramipril to reduce blood pressure and SIMVASTATIN to reduce cholesterol. This drug (Simvastatin) made me so Ill that I couldn't walk up my drive without feeling as if I was going to pass out. I also suffered tummy pains, felt very sick and my heart was thumping and banging like a base drum. Every joint in my body ached so badly that I thought my walking days were over for good. I stopped taking it four days ago and already feel better. My doctor has given me a replacement medicine called PRAVASTATIN but I am frightened to take it, fearing that it may create the same or similar problems. Has anyone got any comments or experienced problems with Pravastatin? I would appreciate any feedback that you might be able to give, positive or negative.
Regards,
Steve.

I just read a few days ago that Merck is trying to get approval for a new drug. It is a combo of Singulair and the Shering pharm. co. drug Claritin. Isn't it nice to know that while we are suffering from this drug, Merck and another pharmaceutical company are trying to make more money on a drug that is supposed to be under investigation. Fortunately, the FDA is not approving it along with a few other drugs Merck is trying to push. This shows us how concerned they are with public health. They would sell us arsenic if they could get approval for it.

Here's a question- What are we supposed to say to our doctors to take this seriously and stop treating it like it's in our heads. Should they check our hormone levels? Have any doctors or nurses ever posted here?

50 yr old female ( gasps @ 5-0 still)

I've been on ToprolXL for some time now. I started with Tenormin and felt FINE! The doctor then decided it was not the 'right medicine' for me and changed me to a 'new and better medication' names TOPROL XL, He started me on 50mg a day. I had experienced rapid heart beat of at least 150 bpm up to 200! My heart had to be stopped in the ER to get it back to being a normal rhythm. At the time I was 39 yrs old :( SCARY! I had every test imagined. Heart tests, lung and leg scans. You name it, I had it done to me ( thankfully, to make sure it was nothing serious). Although I do consider a heart beating that high to be serious! I already have a anxiety disorder, I noticed that my panic attacks are worse now more than ever! I am very very lethargic. Just thinking about doing ANYTHING makes me tired. I even getting tired when I talk too much! My mouth is always excessively dry. I put on weight and even paid for a diet that consisted of 2 'shakes' and one meal per day. Followed it to the "T"! and nothing ?! I've recently read that ToprolXL can lead to all kinds of diseases. One of them being Lou Gehrig's (ASL) :( I am SO very upset that medication is prescribed supposedly to make a person feel better AND I don't think I've physically felt this depleted and depressed in years! I want medical answers and I need support and words of encouragement from everyone that has been on this drug , most especially those weaned off ot it and are on a better drug. Most of the people I notice taking TOPROL XL are taking it fro HBP or symptoms other then the one's I have. I am SO confused now :(

I don't work for another pharmaceutical company. I don't have any competing interests. People keep asking me that. Why? Is everything about competition and money? I am getting sick of being asked that.

Frankly, I don't see how anybody could go up against all of the high powered lawyers that Merck can hire. If anybody wanted to speak about how this could happen, Merck would have people going through their doctoral dissertations looking for plagerism. Plaintiffs would have Merck detectives outside their houses hiding in the bushes. Merck private detectives would interview their friends and teachers.

All I wanted to do was to show parents and patients that they are not the only complaints. These complaints have been reported before. Whether they resulted in any serious warnings to Merck doesn't really make a difference because people know how they feel or how their child feels on Singulair.

There is nothing that we can do, in my opinion, but to believe in ourselves. We might trying writing to Queen Beatrix of the Netherlands that the American sufferers must have Dutch brains--which allow montelukast to penetrate the blood brain barrier and can she do anything for us? This is ridiculous that we should be getting these responses from doctors.

From the Netherlands 2006.
In three of the cases a positive dechallenge was seen.The fact that the patients (except for one) did not suffer from depressive symptoms before they started montelukast, the short latency, and recovery after withdrawal of the drug all strengthen our hypothesis that depressive symptoms are an ADR related to the use of montelukast. According to the Marketing Authorisation Holder of montelukast, depression will be added to the product information.

Mechanism: The mechanism of montelukast-induced depressive symptoms is unknown. However, montelukast has earlier been associated with adverse drug reactions such as abnormal dreaming, nightmares, hallucinations, agitation with aggressive behavior, irritability and restlessness, which suggests that montelukast can penetrate the blood brain barrier and exert an effect in the brain .

http://www.lareb.nl/documents/kwb_2006_4_montel.pdf.

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.

I read these posts and regarding my being quoted as saying that it is unclear whether there are leukotriene receptors in the brain, that isn't true, there are leukotriene receptors in the brain and the relationship between neural systems involved in inflammation and mood is well established. I don't think the misquote was deliberate, I wasnt that definitive when I commented to the reporter on the 'breaking' story (she called me because I had just blogged about it and I updated the blog after I got off the phone). There are a number of parallels with other drugs used to treat medical conditions that have been associated with psychiatric side effects, you can follow the links from the March 27 post "If they dont kill us they will drive us crazy" at
http://www.beforeyoutakethatpill.com/blog.html

Doug Bremner MD

Artie commented below. I am posting Artie's comment back in a place where every one will see because I know the importance of arming yourself with research. I have worked for a major pharmaceutical company in my lifetime. I know that we need research and we need proof. Without that, we will be ignored.

Reply 1 minute ago on Apr 02, 2008 by artie81, #6536
Do you honestly think the people on this forum know how to interpret scholarly journal artcles?

Posted at 6:44 PM on Apr 02, 2008 by concernedcitizen, #29028
A British study suggests that Singulair should be studied for possible psychiatric adverse drugs reactions in children. I don't have this access to this journal so I have to try to find it. I will get back to you on what it says specifically. BMC Clin Pharmacol. 2008 Mar 17;8(1):1 Links Individual case safety reports in children in commonly used drug groups - signal detection.Brunlof G, Tukukino C, Wallerstedt SM. ABSTRACT: BACKGROUND: Due to few paediatric drug safety studies, knowledge on risks of drug treatment in children is limited. The knowledge needs to be increased to make proper risk-benefit analyses possible when treating paediatric patients with drugs. The aim of the present study was to investigate drug groups commonly used in children concerning type and frequency of individual case safety reports in children. METHODS: Number and type of individual case safety reports in the 30 groups of drugs (5th level ATC-code) most sold (number of defined daily doses) in outpatient treatment to children (<5 years old and experiencing psychiatric adverse drug reactions. CONCLUSION: The number of individual case safety reports per million defined daily doses varies in different groups of drugs. A possible signal for montelukast and psychiatric adverse drug reactions was found, which should be further explored. PMID: 18366638 The key sentence is: A POSSIBLE SIGNAL FOR MONTELUKAST (SINGULAIR) AND PSYCHIATRIC ADVERSE DRUG REACTIONS WAS FOUND, WHICH SHOULD BE FURTHER EXPLORED.