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Neurological symptoms symptoms and conditions

Here are side effects posted by other members, that mention neurological symptoms.
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50 Side Effects posted for neurological symptoms

July 23th
2009
9:09 PM

lower back pain, hair loss,joint pain, complicated migraines, vertigo, palpitation, hormonal imbalances (lowered DHEA, increased aldosterone-it affected my adrenal glands and kidneys), epigastric pain, bleeding, extreme fatigue, anxiety,pulmonary failure etc. I had to go through ER, 2 CT scans ( abdominal and brain), 2 MRIs, neurologist, endocrinologist, GI, gyno etc. I threw my Yaz pills in the trash after the first CT scan that revealed multiple tumors in my liver and left adrenal gland ( i took the pills for about 3 and 1/2 years)... the past 6 months have been a hell, but there are no more migraines, anxiety or other neurological symptoms at this point. By the way, one of my best friends who just started on Yaz recently ended up in the ER last week with a blood cloth in her left lung. Please stay away from that drug!

-- By ingridm | Reply | (2) replies | Private Message me

November 4th
2008
11:55 AM

I'm not sure my symptoms are the result of Lipitor, but I sure am going to find out by stopping taking Lipitor for a week. My symptoms - the numbing of my left foot, the reduction of motor skills in the left foot - it comes quickly and stops almost right away. I have been on Lipitor for several years taking 20 mg but recently was increased to 40 mg. I have no other
symptoms. Just touching base. Thanks for the site.

-- By oscar222 | Reply | (2) replies | Private Message me

October 22th
2008
4:57 PM

I am re-posting this from June. I believe that we have many reasons to suspect that Singulair does indeed penetrate the blood brain barrier. I personally believe that under certain unusual conditions that Singulair can cause neurological damage. I tried before to put together a scenario of brain biochemistry that could explain how this can happen. Of course, I am just hypothesizing and all of my ideas will not prove to be totally correct. From the number of postings here regarding neurological symptoms, I believe that there is an answer out there somewhere. Why the FDA is not searching for this answer is a complete mystery to me.

I believe that it is possible that Singulair causes the same biochemical response in the brain that is cited in this study -- thus causing neurological damage.

"Thus, elevated NO production leading to mitochondrial dysfunction, glutamate release, and excitotoxicity may contribute to neuronal death in neurological diseases."

IS SINGULAIR CAUSING THE DEATH OF NERVE CELLS IN SOME PATIENTS? DOES THIS HAPPEN - ALTHOUGH INFREQUENTLY- BECAUSE OF GENETIC OR BIOCHEMICAL FACTORS OR BOTH?

June 12th
2008
2:56 AM
I have stated many times that I am not an expert. I just post what I find. This has been a mind boggling journey for me. This is way over my head but I struggle to read and understand. Finding answers to why children are suffering from neuro-psychiatric side effects is worth the effort.

I have made the following observations.

1. Some quinolines are known to be able to cross the blood brain barrier.
2. Molecules that ionize are known to be more likely to be able to cross cell membranes. So if montelukast ionizes as a result of change in blood pH to sufficient acid conditions, then it could be possible that it does in fact cross the blood brain barrier.
3. We know that there are cysLT1 receptors in the brain.
4. We know that researchers believe that montelukast may bind at the arginine of the cysLT1 receptor.
5. We know that arginine contains four nitrogens. And montelukast contains one.
6. We don't know what happens to those nitrogens. Are those nitrogens converted to nitric oxide?
7. We do know what macrophages create nitric oxide as I posted.
8. We do know that if something cause excessive nitric oxide to build in the brain that there would be damage to the neurons.

Some people may remember when I got stuck at the astrocytes, the cysLT1 receptors and glutamate. I keep looking for research reports that may shed more light on this.

Titre du document / Document title
Nitric oxide causes glutamate release from brain synaptosomes
Auteur(s) / Author(s)
MCNAUGHT K. S. P. (1) ; BROWN G. C. (1) ;
Affiliation(s) du ou des auteurs / Author(s) Affiliation(s)
(1) Department of Biochemistry, University of Cambridge, Cambridge, ROYAUME-UNI
Résumé / Abstract
We determined the ability of pathological levels of nitric oxide (NO) to cause glutamate release from isolated rat brain nerve terminals using a fluorometric assay. It was found that NO (0.7 and 2 μM) produced (4 and 10 nmol/mg of synaptosomal protein) Ca2+-independent glutamate release from synaptosomes (after 1 min of exposure). Spermine/NO complex (spermine NONOate; a slow NO donor) and potassium cyanide (an inhibitor of cytochrome oxidase) also caused Ca2+-independent glutamate release. Preincubation of synaptosomes with 5 μM 1H- oxadiazole quinoxalin-1-one (an inhibitor of soluble guanylyl cyclase) had no effect on NO-induced Ca2+-independent glutamate release. Ca2+-independent glutamate release produced by NO was greater in a low-oxygen medium. NO, spermine NONOate, and potassium cyanide inhibited synaptosomal respiration with a similar order of potency with respect to their ability to cause glutamate release. Because NO has been shown previously to inhibit reversibly cytochrome oxidase in competition with oxygen, our findings in this study suggest that NO (and cyanide) causes glutamate release following inhibition of mitochondrial respiration at the level of cytochrome oxidase. Thus, elevated NO production leading to mitochondrial dysfunction, glutamate release, and excitotoxicty may contribute to neuronal death in neurological diseases.
Revue / Journal Title
Journal of neurochemistry ISSN 0022-3042 CODEN JONRA9
Source / Source
1998, vol. 70, no4, pp. 1541-1546 (29 ref.)

INIST-CNRS, Cote INIST : 4037, 35400007527188.0230

-- By concernedcitizen | Reply | (6) replies | Private Message me

October 22th
2008
4:14 PM

My 5 1/2 year old son began taking 4mg Singulair in the p.m. and an inhaler (asmanex) in the a.m. We were still having trouble controlling the asthma and his Sing dose was raised to 5mg. & within 1 week of the increase he began having terrible facial tics and aggravated behavior (defiant, poor listening, easily frustrated and angered) The tics were in the form of opening and closing his mouth, as if you were trying to clear your clogged ears after a plane flight. This caused him much pain in his jaws and facial muscles, so he would tic and then cry as he was in pain. This ramped up his anxiety and it made the ticking worse. He has been off of all asthma medication (cold turkey) for 5 full days. He has episodes where the tics happen for 10 min -1/2 hr, other times during the day it is one here and one there. He does not want to leave the house to do anything, even his favorite activities. Thank god I found this site (and others like it), as I got some answers and some hope. We went to see my cousin this week who is a neurologist and he never heard of the correlation of Singulair and neurologic side effects like these. He said that (hopefully) the medication side effects will cycle through and resolve the ticking and behavioral changes. If not we are probably looking at a Tic Disorder which is in the Tourettes Family.He put my son on a very low dose of Klonopin to mellow out his anxiety and help reduce the tics, but has only been on it for 1 1/2 days and it usually takes a wk or 2 for full absorption and results.I have since sent him and my pediatrician and allergist links to this site and others. I think that I see some improvement in my son, yesterday I thought he did better and my husband thought it was a worse day, I think we have totally lost our perspective and objectivity on this. If anyone out there has a time frame on when they saw significant recovery and positive changes I would love to hear from you. This is a total nightmare and if it is this drug, someone is going to pay. My prayers go out to all who are going thru this.

-- By stacy310 | Reply | (5) replies | Private Message me

July 5th
2008
6:57 AM

HI guys I was given pred at 60mg then over the next several weeks I tapered off. it is now about 3/4weeks since I took the last tablet. Whilst i was on them I developed quite bad hand tremors/shakes and since taper off to a low dose I have started with muscle twitches all over. Has anyone had experiences like these? And how long did they last?

-- By rhino | Reply | (2) replies | Private Message me

June 12th
2006
7:34 PM

Please help. I took Yasmin for 3 years wothout much problem. Last year I started to get migraines... bad migraines with yucky neurological symptoms.. dizziness, aura, a moment of weird speech. All terrifying possibilities (stroke, brain tumor, etc)were ruled out with various tests. This was so scary that it pushed me into a series of full blown panic attacks. (I had never had a panic attack in my life!) My neurologist suggested I try to get off oral contaraceptives just to see what would happen. He never attributed anything directly, just said that hormones are very powerful substances in the body and it was worth a try. I have been off Yasmin for 3 months. I had crazy PMS last month, depression on and off, muscle pain and MAJOR anxiety. i had to leave a crowded restaurant tonight because I thought I would be sick. I got very hot and jumpy and had to get fresh air. I have never had stuff happen to me like this before. I am terrified. I feel crazy.

-- By kakdavis | Reply | Private Message me

February 28th
2006
6:03 PM

I used Tazorac YEARS ago for bad acne. After starting it (along with Doxycycline), I started feeling "spaced out." I can't really explain it... it felt like I was "floating in a fog." I also was having visual disturbances... kind of "snowy" vision. I discontinued the antibiotics, thinking they were the culprit, but the neurological symptoms continued. When I stopped the Tazorac, the symptoms stopped as well. I had even made an appointment with a neurologist, but didn't actually see the doctor since the nurse assured me that something I used topically could indeed cause me to have neurological symptoms. I was in denial though... thinking that maybe the Doxycycline just needed a while to get out of my system. So I tried the Tazorac again and once again the neurological symptoms reappeared. Needless to say, I got rid of it.

-- By thatkat | Reply | Private Message me

July 16th
2004
1:29 PM

Well, let's hope it is the Zocor, left leg, left arm weakness, no pain, neck aches and stiffness and tingling in neck, funny twitching in calves, burning and just different neurological symptoms. First, they thought stroke, previous heart surgery 8 months ago. Been on Zocor for 8 months. Now, MS or tumor or differential diagonosis, no answers. Have stopped Zocor for 2 weeks, strength has came back neck is still stiff. We will see, pray for us. 42 years old.

-- By sauve | Reply | Private Message me


 

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