Review: could Oxcarbazepine cause Systemic lupus erythematosus?
Summary: Systemic lupus erythematosus is reported only by a few people who take Oxcarbazepine.
We study 2,711 people who have side effects while taking Oxcarbazepine from FDA and social media. Find out below who they are, when they have Systemic lupus erythematosus and more.
You are not alone: join a mobile support group for people who take Oxcarbazepine and have Systemic lupus erythematosus >>>
Oxcarbazepine has active ingredients of oxcarbazepine. It is often used in epilepsy. (latest outcomes from 2,892 Oxcarbazepine users)
Systemic lupus erythematosus
Systemic lupus erythematosus (an autoimmune disease, which means the body's immune system mistakenly, attacks healthy tissue) has been reported by people with rheumatoid arthritis, crohn's disease, osteoporosis, multiple sclerosis, high blood pressure. (latest reports from 13,091 Systemic lupus erythematosus patients)
On Jan, 28, 2015: 2,711 people reported to have side effects when taking Oxcarbazepine. Among them, 1 people (0.04%) has Systemic Lupus Erythematosus.
Time on Oxcarbazepine when people have Systemic lupus erythematosus * :
Gender of people who have Systemic lupus erythematosus when taking Oxcarbazepine * :
|Systemic lupus erythematosus||100.00%||0.00% |
Age of people who have Systemic lupus erythematosus when taking Oxcarbazepine * :
|Systemic lupus erythematosus||0.00%||0.00%||0.00%||0.00%||100.00%||0.00%||0.00%||0.00% |
Severity of Systemic lupus erythematosus when taking Oxcarbazepine ** :
How people recovered from Systemic lupus erythematosus ** :
Top conditions involved for these people * :n/a
Top co-used drugs for these people * :
- Clonazepam (1 people, 100.00%)
- Topamax (1 people, 100.00%)
* Approximation only. Some reports may have incomplete information.
** Reports from social media are used.
How to use the study: print a copy of the study and bring it to your health teams to ensure drug risks and benefits are fully discussed and understood.
Do you have Systemic Lupus Erythematosus while taking Oxcarbazepine?
You are not alone! Join a mobile support group:
- support group for people who take Oxcarbazepine and have Systemic Lupus Erythematosus
- support group for people who take Oxcarbazepine
- support group for people who have Systemic Lupus Erythematosus
Drugs in real world that are associated with:
Could your condition cause:
Can you answer these questions (Ask a question):
- Can you stop trileptal cold turkey?
I ran outta my Trileptal, the last time I took it was in the hospital on Saturday I was there for 2 days and I was normally taking 300mg 2x daily and the hospital gave me 600mg 4x on Saturday and the day before I took the one 300mg I had left in the morning. Since the hospital I have not had any Trileptal to be able to take because they didn't send me home with any because I'm from another State and I'm not sure if that's why but I should have my medicine tomorrow but I feel horrible and I just wanna know if physically I will be alright? Thank you so much and would appreciate a quick responce.
- What can cause trileptal to not show hardy in blood test.
My cousin is handicap but TRILEPTAL not showing in.blood.
- Can trileptal aggravate a gout attack?
Can trileptal raiser ic acid and aggravate a gout attack.
- Crohns disease and deranged lfts diferential diagnosis
Patient with Crohns disease and deranged LFTs first was on Imuran then withdrawn due to unexplained elevated LFTs.nOW On Ramicid still elevated LFTs (high bilirubin (indirect) and ALT .
- Is there a support group in the us for people with insulinomas? (1 answer)
SUPPORT GROUP IN UNITED STATES!!!
Hi, the only support group that I've been able to find for people with insulinomas is located in the UK... just wondering if there is one in the US. I had pancreatic surgery to remove my first insulinoma in 2012, we're thinking there's another because I'm still having problems with hypoglycemia... if anyone know anything, PLEASE CONTACT ME!!! :)
I know there can't just be a support group here for FERRETS!!! people are kind of important... I hate this song, but "Don't worry, BE HAPPY" is okay, I guess... I'm trying to force it upon myself. Things will get BETTER!!!
More questions for: Oxcarbazepine, Systemic lupus erythematosus
You may be interested at these reviews (Write a review):
- Had nms in 2005, will trileptal increase chance of recurrence?
In 2005 I had NMS, which was not detected by my drs for 4 months. I'd been on Lexapro & Seroquel for 2 yrs, but was weaned from Lexapro & placed on Lamictal 3/05. Began getting low-grade fevers, which I was told were not caused by the Lamictal. I quit taking it anyway, fevers (along with uncontrollable shivering) continued & got higher. By 5/05 my temps were reaching 105 deg F. Husband said I became combative, refused to go to hospital. Early June/05 he came home to find me wrapped in blankets, with a temp over 105 F. He tried to place me in a tub of cold water, said I was rigid & screamed when he tried to move me. I was in the tub, speaking "in tongues" (his description, I have no memory of this). He called 911, took me to hospital. I woke, no idea where I was or why. After a lumbar puncture & 2 days in ICU I went home. The fevers continued...2 weeks later he came home to find me wrapped in sheets, towels, blankets, with the heat on full (it was in the 90's outside) he called ambulance again. I awoke to find myself under an ice blanket with nurses pushing large vials of dantrolene into both arms, several liters. Another LP, a stint in ICU...this time they told me it was NMS. The dr who dxd me said he was surprised I was alive, & not a vegetable, as my temp had peaked at 109 deg F. I suffered brain damage; short-term memory loss, brain can't control my body temp, my blood pressure went up. An arteriogram showed completely healthy heart & arteries, no plaque at all. I lost all body fat as well as some muscle mass. The fevers continued even after stopping the Seroquel. I visited my PCP for a checkup in 9/05, temp was normal. I started shuddering, my temp went up a full degree every 5 minutes. PCP admitted me to ER, my heart rate was over 272 B/M; they stopped my heart 3 times to "reset" it, which didn't work. I spent 3 days in hospital. Several months later my P doc tried me on Lamictal alone; I got Stevens-Johnson syndrome. I stopped the drug as soon as the signs appeared. I've been untreated, except for Neurontin & Primidone, until my manic episodes became unlivable. 3 weeks ago I went 8 days with no sleep, became psychotic. My P doc gave me Trileptal, which has evened my moods, but I've been getting low-grade fevers (highest was 103.6). Would having had NMS in the past make me more prone to falling to it again with the Trileptal? It's the only new med I've taken in over a year.
- Could trileptal cause benign intracranial hypertension
My Daughter is 9 and was on Trileptal for three years and just started to have severe headaches that lasted for two weeks and were quickly and poorly diagnosed as a status migraine. Another week of pain and incorrect treatments finally led to more tests and the correct diagnosis of IIH. Supposedly the most susceptible person (1 in 5,000) to get IIH in the US is an over weight female in her 20's. Based on my daughters information and the information on this site, Female Trileptal patients appear to have a 1 in 1500 chance of IIH and if you are female and also aged 2 to 9, your chances are about 1 in 250. Or 20 times more susceptible than heavy, adult females.
- I have less pain from my trigeminal neuralgia when i'm manic.
Has anyone had a relief of pain when they are manic?
- Lupus induced by amoxicillin (1 response)
Was given Amoxicillin for Strep Throat and on day 10 I noticed a rash starting on my torso and began to feel ill, as if I had the flu. Went to emerg and got sent home with Benadryl. Woke up the next morning to the rash getting worse and an overall feeling of fatigue. Went to emerg again and this time had blood taken and the results showed an extreme rise in my white blood cells and by then, I had a fever. I was airlifted to another hospital where they did tests, but really had no idea what was wrong. I discharged myself with a script for corticosteroids and by then my joints began to stiffen, to a point of barely being able to walk and the pain was excruciating! I had to be cared for by my husband and struggled to lift my tea cup, or get out of bed. This lasted for about a month and then gradually began to subside. The doctors never did have answers for any of it. They chalked it up to an allergy to Amoxicillin. One mentioned "Steven Johnson Syndrome".
- Serious oxcarbazepine (trileptal) side effect
My mom suffered from acute facial nerve pain for almost last 8 years which was diagnosed for Trigeminal Neuralgia. The pain started suddenly and she started and continued the treatment with Lyrica. In the beginning, the pain would go away after several months and start again in a year or two. However, the intervals between the pain periods narrowed until they became more often despite the fact that she was never off the adjusted dosages of Lyrica. what's more, her Dr. added Oxcarbazepine (Trileptal)as he lowered the Lyrica as the result of extreme sleepiness side affect for Lyrica.
As the pain continued without relief, the dosages also adjusted. However, she started a severe case of muscle jerks whenever she moved around like standing up, walk or used her legs or hands. She was not able to live without constant assistance due to the sudden unpredictable muscle convulsion / jerks (similar to "knee jerks" when stimulated). None of the dr.s could determine what was going on. Until ONE Neurologist who treated my mom during her hospitalization following a fall, said that the muscle jerks/convulsions were noted as drug Trieptal side effect. NO WHERE and NO other source my family or I had ever come upon warned about this. That Dr.'s opinion was CONFIRMED when my mom started to slowly get off the Trileptal. Unfortunately, I still haven't seen any warning about this side effect related to the Trileptal. Of course, we are aware of the fact that not every patient might not have affected by this side effect, however, as long as that Dr. advised us and the symptom does subsiding by Trileptal/oxcarbazepine dose reduction from my mom's medication, I think this is necessary to be immediately addressed and studied by the medical society and the Pharma. co. who is making the drug.
More reviews for: Oxcarbazepine, Systemic lupus erythematosus
Comments from related studies:
From this study (1 week ago):
Constantly flapping hands, rocking while sitting
From this study (2 weeks ago):
Muscular weakness developed while under trileptal but remained after discontinuation (8 months, terminated April 2013). Recent diagnosis of FSHD, link with TN?
From this study (1 month ago):
elevated liver enzymes and hyponatremia
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