Singulair and meltdown

My son started taking Singulair in Sept 08 when he was 22 months old. I never really gave it to him consistently, since it was just to help with his reoccurring ear infections. I noticed a little change in his behavior, but I thought it was the "terrible two's". I started giving it to him religiously at the beginning of Nov 08. He had his first meltdown on Nov 15. He was totally uncontrollable. I call it the "Exorcist" tantrum. I took him to the ER, but they told me nothing was wrong. (I did tell the ER all of the medications he was taking.) He started waking up in the middle of the night screaming. Each day, he got a little worse. Defiant, hateful, destructive, etc. He still isn't talking much, so he can't tell me what is going on. Christmas and New Year were horrible. We had NO idea that it could cause mood changes (that is putting it mildly). The pediatrician had no idea what could be causing the behavioral changes. He also started biting his fingernails and obsessing over little things, like the strings hanging off of his blanket.

We decided to take him off Singulair after double checking the side effects. We stopped a week ago, and the change is amazing. He is back to my great little boy. I am sooooo glad that we discovered this after only a few months. I cannot imagine living like that for years.

Two days after stopping the Singluair, I found this website: ******

As I read the different cases, I thought that it was exactly like my son. I was convinced it was the medicine. Each day that he gets better and better-like his normal self- I keep getting madder and madder that no one informed me about the possible side effect. The Dr. did not know nor the pharmacist.

Yesterday, I went to the FDA site to complain about the side effects. It just so happens that the FDA released a statement yesterday that they are still investigating the link between suicidality and Singulair.

We need to let everyone know, that if you are using Singulair, please pay attention to their child's behavior. Some people may be just fine, but others (like my son) are not fine.

PRAISE GOD for all of the stories shared on this site. And I've only read page one. My husband called me back today to say that he "googled" Singulair and found some interesting things (to say the least). While we were on the phone, my three-year-old was in the throes of another meltdown, kicking me, hitting me, throwing whatever he could get his hands on. My older two boys, 8 and 12, were ordered, once again, to lock themselves in their rooms to avoid being hurt by him. He will throw stuff, bite, hit, kick, and, at times, spit on us. This disturbing behavior is rather constant lately. He is like a mad man. Very scary.

Caleb has been on Singulair since about age 1, when he was diagnosed with chronic sinusitis and allergic rhinitis. Unfortunately, we initially equated his rages with the onset of "terrible two's" and dismissed his behavior to a chorus of "oh, he's just a boy!" My husband felt, at times, that I was just not disciplining him properly. I intuitively knew, having raised two other boys, that this behavior was abnormal, even for severe tantrums. We received a variety of suggestions from his pediatrician, caregivers, and grandparents, all to no avail. We have several calm days but things always deteriorate back to insanity. He is VERY unpredictable.

Last Thanksgiving, Caleb (age 3) was kicked out of his daycare setting for biting and hitting. Once I witnessed him run as fast as he could into a group of playing children, falling on them, kicking them. He would walk up to sweet little girls half his size and push them down as hard as he could. It was a nightmare. My husband had to take 3 weeks of leave to stay home with him while we prayed and searched for new care. We had him evaluated and he was staffed into the "developmentally delayed" program in our school district (for poor adaptive skills and personal/social behaviors). We recently had his tonsils removed, hoping that some of the sinusitis symptoms and behaviors would improve. They really haven't. This past week we have been looking into the Feingold diet. We have been PRAYING for answers. The last time we spoke with his developmental neurologist, he recommended a trial of Risperdol (sp?). We feel like more meds would be like a band-aid, not a solution. But his rage is becoming unbearable.

So, that brings us to today. I was so moved by your accounts. Unlike so many of you, we don't have much of a "before" to go by. But his "after" sounds VERY much like what you have all described. It's probably the pure rage that I see on his face that is the scariest part. And at the same time he seems desperate and vulnerable. He truly seems to snap. If we had pool chairs, I can just picture him throwing them (citing another post :).

We are going to throw the Singulair away. He will never, ever have it again. Even if this isn't the cause of his problems, I certainly don't want to exacerbate any behaviors with this toxic medicine. I will post again just to let anyone who's interested know if this changes his behavior. I am praying that my entry will help someone else, just as all the other postings have helped me. I have renewed hope.

I have copied many of your comments to a Word document. I will be sharing it with a high ranking officer at the medical clinic/hospital on Keesler Air Force Base. I hope that he will discuss this with his staff and that perhaps we can at least make a difference here. I, too, will be filing a report with the FDA. I can only pray that this medicine has not permanently altered his developing brain.

Our son was put on Singular almost 2 years ago to help with his "moderate" asthma. It has been the hardest 2 years for our family. My son who was already very senstive became very depressed. He showed no interest in anything. He was always sad and very down on himself. He had awful night terrors/nightmares. He didn't want to go to school or do anything. We continued to sign him up for sports/piano/scouts and it was a battle to get him to go. He always had headaches, which I thought were because of dehydration and made him drink water. We had him seeing a therapist trying to help him with the sleeping problems and the depression. We switched his room with his sister to physically make him closer to us at night. He was anxious and very irritable. If something went wrong, he couldn't handle it and had complete meltdowns. If he didn't eat anything for a while and his blood sugar got low, he was uncontrollable. To add to the problem was he was never hungry so I would have to force him to eat something about every 2-3 hours to prevent the meltdown.

The good news is that he has been off of Singular for over a month now and he is a new kid. He is excited to go to practice and will ask his dad to play catch with him in the yard. He is happier and we have not heard once "this is the worst day ever" which we had heard all the time before. He has not had one headache and seems to have a little bit of his appetite back. He is happy and holding his head high. Now, he still doesn't want to go to school (what 8 year old boy does), but he doesn't fight me when I tell him it is time to go. He does not have the meltdowns or the irritability. He even showed some empathy to my husband last week.

My husband and I are amazed at how different he is. We are also very upset that for almost 2 years we made his life miserable by forcing him to take this drug. I think for kids that are already sensitive to things it heightens everything! I am filing a complaint with the FDA and spreading the news to all my family and friends. I hope this information helps! I know I have learned a lot from reading these posts.

The doctor told me yesterday it could take up to 6 weeks to get this drug completely out of his system. he is now 5 days off and everyday there is some glimmer of my son shining through. the best way to express it is peace or calm. he is calmer when things go wrong that before would have caused a meltdown.

I counted over 20 things that he has suffered with that I see other children have had to deal as well. I have to be hopeful given the little glimpses of change I am already seeing.

Thank goodness I found this site!!! I was starting to think I was going crazy! I have been taking Singulair for a little more than 3 weeks, for my allergies. It works wonders on allergies, but I have had several side effects, that I hadn't realized were side effects until reading this site.

I have felt very tired, yet anxious at the same time. I've been very moody, almost to the point that I feel angry all day (which is very unlike me). I have also had strange aches and pains, along with itchy skin on my feet and under my arms. I have also had very vivid dreams. Strange, bad dreams, that last all night long. When I awake I feel like I haven't had any sleep.

I am going to stop taking Singulair today!