Review: could L-glutamine cause Migraine?
Summary: there is no Migraine reported by people who take L-glutamine yet.
We study 203 people who have side effects while taking L-glutamine from FDA and social media. Find out below who they are, when they have Migraine and more.
You are not alone: join a mobile support group for people who take L-glutamine and have Migraine >>>
L-glutamine has active ingredients of glutamine. (latest outcomes from 224 L-glutamine users)
Migraine (headache) has been reported by people with multiple sclerosis, birth control, depression, osteoporosis, pain. (latest reports from 51,717 Migraine patients)
On Feb, 27, 2015: 203 people reported to have side effects when taking L-glutamine. Among them, 1 people (0.49%) has Migraine.
Time on L-glutamine when people have Migraine * :
Gender of people who have Migraine when taking L-glutamine * :
Age of people who have Migraine when taking L-glutamine * :
Severity of Migraine when taking L-glutamine ** :
How people recovered from Migraine ** :
Top conditions involved for these people * :n/a
Top co-used drugs for these people * :
- Inositol (1 people, 100.00%)
- Diazepam (1 people, 100.00%)
- Reishi mushroom extract (1 people, 100.00%)
- Ginko biloba (1 people, 100.00%)
- Cytomel (1 people, 100.00%)
* Approximation only. Some reports may have incomplete information.
** Reports from social media are used.
Do you have Migraine while taking L-glutamine?
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- support group for people who take L-glutamine and have Migraine
- support group for people who take L-glutamine
- support group for people who have Migraine
Drugs in real world that are associated with:
Could your condition cause:
Can you answer these questions (Ask a question):
- My daughter has congenital php and diabetes(hyperglycemia) not diagnosed until 18.with both...now 23...blood sugars are uncontrolled nothing so far is helping
All the patients I have chatted with have LOW blood sugar but mine is high. Nothing is helping it just keeps climbing. What gives?
- Can omeprazeloe cause muscle loss?
Previously to taking Omeprazeloe I had normal bowel movements after getting control of the diarrhea caused by the irritable bowel syndrome. The day after I took the first capsule I experienced extreme constipation. It was hard to have a BM and had to go several times. It has caused bad abdominal pain. I started to have hair loss. It has thinned to half as much as I had. My migraines came on like crazy. I lost eight pounds over about a month after I stopped taking it. I lost fat I had gained in my abdomin but also my muscles have deteriated some. I would recommend that no one takes this medication and it should be taken off the market. People who have suffered from taking this medication should be compensated.
- I have had the history of seizures, kidney stones, high blood pressure and migraine headaches. i am soon going back to school and need something to help with memory . what is best to help in this way
Not sure what I am suppose to write here. My mind is never clear and it feels as if there is swelling that keeps me from wanting to learn or work. Taking IBprofen helps take some of the swelling away but not all.
- Why when i have a migraine i feel the need to eat more and more? (2 answers)
Can someone please help me why when I get a migraine I have the need for excessive eating? I get the feeling that if I eat more I will feel better. I am now 43 years old woman and my migraines the last three years get worse and worse. Both more intense and more often ( like twice or even three times a week). I am on Effexor that is treating depression 75mg per day. Can someone advise me what can I do? I feel so much helpless and frustrated as my quality of life has deterioted so much.
- Is it my thyroid or am i mentally ill? diagnosed w/ hashimoto's thyroiditis but untreated - chronic pain unmanaged also (2 answers)
I moved to OR from HI and brought all my records, signed releases, and had many diagnoses, all but the thyroid, was being treated and long-term. I also took Oxycontin & Oxycodone for severe chronic pain from bilateral SI joint fusion (right screw protrudes & leg also becomes numb and weak with activity) & lumbar and cervical degeneration & facet arthropathy. I had volunteered reducing dosage as I'm always trying to reduce Rx intake to alleviate side effects (I am tiny, even for a youth & adult dosages seem to drug me). Next month, it was known that I could not function well because pain was not managed, but needed to resolve it in OR, as moving. OR Drs. refused to return me to higher dosage (taking minimalist Oxycontin 10 mg CR & Oxycodone/Acet 5mg). After being unable to get up to go to bathroom, walk, contacted adult services to see about in home services & possible foster care placement for young son since I was losing independence & failing in general health & cognitive functioning. I was forced to take bottles of OTC Tylenol to function, with Dr's knowledge, & knowing I had past lesions on liver to follow. Several months later had follow up liver ultrasound, & new small lesions found on liver. After emailing dr about from DHS questioning failure to manage my pain vs. conditions that were disabiling, 6 months later, dr told me I was experiencing withdrawals every morning & finally agreed to increase Oxycontin to 15 mg, which has enabled me to tolerate the pain & function. I have been treated as a drug-seeking patient since attempting to transfer my care.
I have multiple autoimmune conditions, most of which I no longer treat with Rx as I have been overmedicated & side effects are too numerous. So I actually am opposite in many ways. I stopped Lyrica, Silenor (sleep), Elmiron, Bentyl, Dexilant. Stress affects me seriously since I had a TBI and experience anxiety stress disorder, which seems to contribute to auto immune responses. But still knew triggers & familiar with self - this thyroid diagnosis & symptoms experienced new & too destabilizing to live.
Diagnosed w/ Hashimoto's thyroiditis after 1/2 thyroid removed Nov 2011; my antibodies are unbelievably high. I declined in thinking, memory, anxiety-unable to think/track, losing most,getting lost driving, sleep very dysfunctional, too emotional, crying easily & often (unusual for me). I feared losing ability to live independently. My maintenance Rx (Silenor, Lyrica) seemed to drug me. I tried to explain to drs. that I needed thyroid replacement hormones that I never had these problems before.
They referred me to a psychiatrist for medicine management consultation, who gave me mental health diagnoses (histrionic personality disorder, somatoform (hypochondria) that discredited me & ruined my medical records for future validity. Is it thyroid symptoms? Was unmanaged pain contributing? Too much Tylenol? What does a dysfunctional thyroid do to a person? How do I get my medical record addressed to reflect accuracy?
More questions for: L-glutamine, Migraine
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- Imetrix verses butalb/acet/caffeine
I have taken both Imitrex and Butalb/acet/caffeine and I have to say that Imitrex works far better than the other one! The substitute I was given for Imitrex doesn't even touch my migraine pain.
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Wheezing noted by primary physician in this non-smoker. Stopped Topamax per doctor's instruction. 48 hours later was examined by physician and noted that wheezing stopped.
- Review: could lyrica cause intracranial pressure increased?
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- Bad side effect of melatonin/imitrex use together
I have taken melatonin for insomnia I've been experiencing recently (not a chronic condition). I haven't had any problems or interactions with my other regular medications while using the melatonin, other than drowsiness in the morning. Last night I had a migraine at bedtime, so took 50 mg. of imitrex, my usual dose for one. Since I haven't had one during the period I've been taking the melatonin I feel fairly confident in assuming that my symptoms were a result of the combination.
I was awoken--thank god!--by choking on my own saliva and almost vomiting. I was able to go back to sleep--lying on my side to avoid aspirating anything--and was awoken again several hours later while I was wetting the bed!!! Incontinence has never been an issue for me (well, not since I was 3, I imagine) and I was really shocked. Although I immediately got up to clean the bed, I was so sleepy that I got back in (on the dry side :) and slept for another 4 hours.
Although, as I mentioned, I think it's likely that the problem was the result of an interaction with the Imitrex, which has a soporific effect, I'll stop using the melatonin to be safe!
- My reaction to talking sumatriptan for the first time.
after 10 minutes of taking the sumatriptan tablet i got all of the symptoms i stated and from those i developed a rare movement disorder called 'Dystonia' that has affected my right foot making me unable to walk and my right hand making me unable to write.
More reviews for: L-glutamine, Migraine
Comments from related studies:
From this study (2 days ago):
I have had C-diff since 9/3 2014. I am on my 5th reoccurrence of it, and I took flagyl twice and vancomyacin with the secondary medication. no relief. Ended in the hospital with dehydration, lack of potassium and felt horrible.
My moods, have been up and down, since I just came down with a bladder infection two weeks before my fecal transplant and it took them a week to give me the antibiotics. They gave me bacteria, and all of the sudden on the 4th day my knees hurt, my upper thighs. I do wonder what is wrong. I have always been a very compliant do not complain patient but gosh, I feel like I am going to die from .
I do not know how I can continue to work?
From this study (2 weeks ago):
Daily headaches told by neurologists chronic
From this study (2 weeks ago):
Though I've always been prone to dry eyes and migraines (not an more issue than in past) since starting my new job I have my dust allergies and fluorescent lighting to contend with - postal outlet. Where I used to be able to work on computer for a few hours before my eyes went "crazy" it's only about 15 minutes now. I depend on being able to work on my computer as a photographer and writer. Not to mention communication via FB and emails. It also has stopped me from doing some online things that are work-related. I can't even watch a movie on the computer for long before my eyes are affected. I've always had a "constant headache" when I am asked to focus on it. I wouldn't call it a headache but a dull pain/pressure in my head. Different from my migraines which are largely hormonal. I've had an ocular migraine which scared the shit out of me, and when I discovered it could be caused from my birth control I stopped that! I haven't had one since.
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