Review: could Remicade cause Acute psychosis?
Summary: Acute psychosis is reported only by a few people who take Remicade.
We study 85,089 people who have side effects while taking Remicade from FDA and social media. Among them, 3 have Acute psychosis. Find out below who they are, when they have Acute psychosis and more.
You are not alone: join a mobile support group for people who take Remicade and have Acute psychosis >>>
Remicade has active ingredients of infliximab. It is often used in crohn's disease. (latest outcomes from 85,494 Remicade users)
Acute psychosis (period of mentally unstable behaviour) has been reported by people with depression, pain, schizophrenia, psychotic disorder, hiv infection. (latest reports from 1,316 Acute psychosis patients)
On Jan, 3, 2015: 85,089 people reported to have side effects when taking Remicade. Among them, 3 people (0.00%) have Acute Psychosis.
Time on Remicade when people have Acute psychosis * :
Gender of people who have Acute psychosis when taking Remicade * :
|Acute psychosis||100.00%||0.00% |
Age of people who have Acute psychosis when taking Remicade * :
|Acute psychosis||0.00%||0.00%||66.67%||33.33%||0.00%||0.00%||0.00%||0.00% |
Severity of Acute psychosis when taking Remicade ** :
How people recovered from Acute psychosis ** :
Top conditions involved for these people * :
- Sedation (2 people, 66.67%)
- Crohn's disease (2 people, 66.67%)
- Contraception (1 people, 33.33%)
- Prophylaxis (1 people, 33.33%)
- Colitis ulcerative (1 people, 33.33%)
Top co-used drugs for these people * :
- Asacol (2 people, 66.67%)
- Acetaminophen (2 people, 66.67%)
- Propofol (2 people, 66.67%)
- Alfentanil (2 people, 66.67%)
- Mercaptopurine (2 people, 66.67%)
* Approximation only. Some reports may have incomplete information.
** Reports from social media are used.
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Do you have Acute Psychosis while taking Remicade?
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- support group for people who take Remicade and have Acute Psychosis
- support group for people who take Remicade
- support group for people who have Acute Psychosis
Drugs in real world that are associated with:
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Can you answer these questions (Ask a question):
- How many/what percentage of older males who have had a stroke, have another while taking uloric?
Concerned as my Rheumatologist wants me to start using Uloric40 mg and while I see that their is a relatively small incidence of stroke occurring (unless you are part of the "small" group); I have been unable to locate statistics for those previous stroke patients that are now using or have used Uloric, and had another stroke.
- How do i at least try to get the psychiatrist doing my follow up assessment to consider the possibility that the mirena iud was the cause of the acute psychosis i experienced?
I had a Mirena IUD inserted on December 9th. Insertion was fine (but I think I have a pretty high tolerance for pain); but things started going downhill fast. On December 15th I had a blackout drunken episode and in January I had two puffs of a marijuna joint and believe I went briefly Psycotic. I've tried marijuna at most maybe 10 times in my life and aside from once in Amsterdam over 10-years ago (where I likely had more than I should have); I get nothing out of it, don't see what the point is (aside from the possibility maybe I'll realize what all the fuss is about and I might eventually find it relaxing? Thus the ~9 other lifetime attemts.
I just attributed both of these events to bad behaviour and too much alcohol (blackout drunkeness is not new to me, nor are mental health issues). But things have been very stressful in my life, as owing to my personality and upbrining I am just an anxious person and I have some stress management issues. I like to think this is relatively normal human behavior and not means for locking me up and lecturing me for getting someone to buy me a $10 phone card when the call was worth over $100 and I likely make more money than any of the nurses that are working in the psych ward. But alas I have been labelled bi-polar and someone with mental healt issues so I must be both (a) an excessive spender and financially irresponsible and (b) paranoid and dellusional when I believe I have a well paying job (sorry small rant break...)
Anyway starting ~early-mid January I started waking up really early. Not a big deal for a few weeks and I am generally a 'bad' sleeper but generally that manifests itself in having a hard time falling asleep, not staying asleep until the morning. I kept waking up earlier and earlier and sleeping less each night, this early waking up (at first 5am, then 4am and in the last few days before I was locked up, more like midnight after ~1 hr of sleep) happened to a much lesser extreme in 2011 with my first real noticable experience with 'elevated states' of mental health; it was terrifying then because I didn't understand if I was going crazy or just making stuff up in my head (to get attention? I don't know, but I don't have the most consience ingrained 3-meals/day eating habbits at the best of times and after long enough with no sleep I no longer feel hungry and I have to consciencely remember that I should eat and I think I've gone days without food in these states. Eventually in 2011 after too long with not enough sleep (and feeling wired, but not generally exhausted) and after consulation with various phone crisis lines I took myself into the ER to get checked out. I came with a binder of notes regarding my mental health history (mostly self observed and not in my medical files anywhere except for the 2008 ER visit and subsequent 'mild depression' diagnosis) and they were great because they listened to me and did not discount everything I was saying just because I have mental health issues. They also were not willing to provide any official diagnosis, even after a number of follow up sessions. I also very much appreciated this because I don't believe there is a whole lot of value to mental health diagnosis aside from necessairy critical assessments and short term action plans; however I don't know (or don't believe owing to my experiences and general 'normailized' cynical outlook on life?)
I was referred elsewhere for official assessment and subsequently my diagnosis of mild depression and drug regime of antidepressants changed to a bi-polar II dignosis coupled by a doctor who provided 'drug therapy' in the form of lithium and some other mood booster; regular blood tests and monthly lectures wrt if I was aware smoking was an unhealthy activity (yes I have mental health issues, but that does not mean I am stupid nor illeterate; I believe the knowledge that smoking is not healthy has been generally widly accepted as truth long before I was born. i don't actually smoke becuase I think it's the healthiest thing I could ever do for myself!!!). I was either told (or it was just the message I received from the experience?) that I basically had to be on lithium for life, there was no better alternative. This doctor diagnosed me based on the ER medical records; he diagnosed me without even ever talking to me and he never bothered to consider any other options and/or assessments. I am bi-polar II, I am no longer normal or human or really a valuable memeber of society, I need to be drugged so I don't become even more of a problem to society.
I don't think lithium ever did anything for me, I don't think it did anything to me aside from confusing me and allowing me not to have any confidence in myself and my own ability to manage my health or that the meditation/sun lamp therapy/CBT and other various techniques I started were of any value. I do believe that the antidepressants helped me; but I'm not sure if it was the actual drug or just the placebo effect that gave me hope and allowed me to pull through a 9-month period that made me believe that I really wasn't a valuable memeber of society. But if that's the message I have I don't see why I would stick around in society and waste everybody's time just to be a worthless druggie. I don't see why it's such a horrific thing that I've done, smoking pot ~10 times in my life and using alcohol and ciggarettes to self medicate; these are terrible things that I've done I should stop all of this and become a worthless, lesser version of myself and a prescription-druggie. If it comes in a bottle at the drug store, then it's definitly 'good' drugs?
Anyway, I was definitly not in a good place mentally but I stayed at home riding it out (using non-mental health help lines to benchmark my physical condition; which I've given some stress with no sleeping and little eating and generally just being stressed out). I've been making decisions on which is the best of all my bad options with a timeframe that kept shrinking (e.g. warm bath is good because it calms me down, but it's bad because heat is problematic and makes the rashes worse which will add at least a little anxiety for a few hours after the bath; wine makes me a little less anxious so I'll drink it when in this state; but I can't afford not to be aware so I can't get drunk so I drink it slowly, maybe I'll have a small buzz on, maybe a little drunk enough to allow myself to go to bed and help me fall asleep - yes, not ideal but how is this better than being on the drugs they kept feeding me in the psych ward that after the first (maybe second?) night that they did help me sleep at night I felt nasuated, confused, dull and stupid? Why is it ok for other people to drink way more than me and have worse hangovers for the next day but I should get the message that I should never drink alcohol but I should always feel worse than horribly hungover so I don't ever cry, snap at someone too loudly again because I might hurt someone's feelings?
I was planning to go to the ER if that's what my friends and family doctor wanted me to do, owing to my state. I already know I can manage this better and I already know at that point none of the 'professional's' are likely to believe anything I say so I doubt anyone will pay heed to my suggestions that this IUD had any effect? I was admitted to the psych ward but unfortunatly my timing was terrible - it was march break, a lot of the psychiatrists were off skiing so no one could give me any clear indication of when, if ever I would be assessed. I saw the last 30 years flash before my eyes and I can see all of the terrible ways I've been treating myself, I also now believe I was likely sexually assulted by my peditrition (which might explain some of my angst wrt doctors and hospitals and the terror of being locked up in one?) but they told me I was not a good candidate for one on one therapy. I'm posting this annonynously but it's not really something I want to start looking at in detail in a group therapy setting, is that crazy? I'm worried I will be given yet another diagnosis and told I need to take drugs; which will likely make my short term disability claim be denied (as I don't intend to comply with this action plan), and I can't find much on the internet aside from personal experiences individuals have posted wrt the Mirena IUD and psyhcosis so I can't imagine the phychatrist will be interested in listening to my opinion.
Do I need to go back to school for 8-years and get a PhD in psychatry before anyone will believe I am 'qualified' to assess what I know of myself, given that I am the only one who might have a hope of understanding exactly what has happened in the last 30+ years? Can anyone help me in my fight to be myself rather than a prescription-druggie duller and much less interested version of myself that I know I don't like?
- Is it safe to take pravastin while on remicade?
I have just started on Remicade and this drug scares the heck out of me! However it is being used as a last resort as no other medications were bring my ulcerative colitis under control I am very concerned about drug interactions and can't seem to get any straight answers from my doctor or the pharmacist. My main concern right now is can I safely take Pravastian due to being on Remicade? My cholesterol is very high.
- Remicade or ulcerative colitis causing joint pain?
Im also on mesalamine, 6 mp and trazadone. Ive had joint pain in elbow before but i realised it was caused by taking cortenema. I stoped the med and pain went away. After my first infusion of remicade (2days) i started with the knee, ankle, elbows , wrists and hands pain. The more i do. The worst the pain gets. Dr seemed to think it was caused by the UC but the timming of when the pain started is too close to e remicade. Ive had 3 doses. Still in pain every day. UC symptoms are much less severe than before. So why would the UC cause my joint pain?
- I am experiencing myelodysplastic syndrome symptoms but it is said that it doesn't typically get diagnosed for people my age. although everything is spot on and i need to know whats wrong.
I have been doing remicade treatments for about four years now. Lately I have gotten a UTI, an I get random bruises every single day, I also get super tired, my body aches, and I get fevers for hours on end without them breaking. I have no idea whats wrong because this has never happened before but someone told me that it looks like MDS and I looked into it and I have all the symptoms just am not in the age group for it. I was hoping someone would know if there is anything else I could look up. I am aware that remicade long term wise can cause leukemia and that is why this is such a huge concern. Please give me feedback thank you.
More questions for: Remicade, Acute psychosis
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Comments from related studies:
From this study (4 days ago):
First Remicade treatment on Dec. 24th 2014, moderate bleeding persisted, Second Remicade treatment on Jan. 8, 2015, severe bleeding occurred 12 hours after Remicade infusion.
From this study (3 weeks ago):
Also chills fever runny nose and bad cough and sore throat
From this study (3 months ago):
Acne isn't severe in that it is vast, but what I do get is large spots that resemble whiteheads, but deep beneath the surface. They stick around for months without ever changing or coming to a head. Sometimes they itch.
My idea of severe weight gain: 25lbs in 6 weeks.
dzymay on Sep, 12, 2014:
I have also noticed that I have been getting hard pimple like bumps on my face and neck. They never come to a head can be painful to touch and they get big like a boil but they don't go completely away they shrink down to where you can't notice the huge bump but when I rub my fingers over the area you can still feel a little bump under the skin almost like a cyst! What exactly are they and how can I stop getting them?
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