Review: could Magnesium oxide cause Vasculitis?
Summary: Vasculitis is found among people who take Magnesium oxide, especially for people who are male, 60+ old, have been taking the drug for < 1 month, also take medication Nitroglycerin, and have Uterine leiomyoma.
We study 4,680 people who have side effects while taking Magnesium oxide from FDA and social media. Among them, 6 have Vasculitis. Find out below who they are, when they have Vasculitis and more.
You are not alone: join a mobile support group for people who take Magnesium oxide and have Vasculitis >>>
Magnesium oxide has active ingredients of magnesium. It is often used in constipation. (latest outcomes from 4,781 Magnesium oxide users)
Vasculitis (inflammation of a blood vessel or blood vessels) has been reported by people with rheumatoid arthritis, high blood pressure, osteoporosis, multiple sclerosis, depression. (latest reports from 8,109 Vasculitis patients)
On Feb, 13, 2015: 4,677 people reported to have side effects when taking Magnesium oxide. Among them, 6 people (0.13%) have Vasculitis.
Time on Magnesium oxide when people have Vasculitis * :
|< 1 month||1 - 6 months||6 - 12 months||1 - 2 years||2 - 5 years||5 - 10 years||10+ years |
Gender of people who have Vasculitis when taking Magnesium oxide * :
Age of people who have Vasculitis when taking Magnesium oxide * :
Severity of Vasculitis when taking Magnesium oxide ** :
How people recovered from Vasculitis ** :
Top conditions involved for these people * :
- Uterine leiomyoma (2 people, 33.33%)
- Contraception (2 people, 33.33%)
- Mantle cell lymphoma (1 people, 16.67%)
- Heart transplant (1 people, 16.67%)
- Rheumatoid arthritis (1 people, 16.67%)
Top co-used drugs for these people * :
- Nitroglycerin (2 people, 33.33%)
- Magnesium [magnesium oxide] (2 people, 33.33%)
- Ascorbic acid (2 people, 33.33%)
- Lovaza (2 people, 33.33%)
- Yaz (2 people, 33.33%)
* 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 Vasculitis while taking Magnesium Oxide?
You are not alone! Join a mobile support group:
- support group for people who take Magnesium oxide and have Vasculitis
- support group for people who take Magnesium oxide
- support group for people who have Vasculitis
Drugs in real world that are associated with:
Could your condition cause:
Can you answer these questions (Ask a question):
- Can magnesium cause a false positive for thc
i was given magnesium iv in the hospital and mt drug test came up postive for thc
- Do hot flashes go away after taking doxycycline?
I was prescribed a 30 day round of doxycycline to treat a skin infection. I started getting 5-10 mild hot flashes daily right away. I am a fit and healthy 46 year old woman and have never had hot flashes before starting this antibiotic. I didn't see hot flashes in any of the side effects, so I'm wondering if it's related or if it might be something else (menopause) that will continue after I'm done. Would like to hear if others had similar experiences.
- Is it safe to take zofran and magnesium citrate?
Is it safe to take magnesium citrate for constipation and zofran?
- Can low dose hrt cause schambergs disease
For 10 years I have been suffering from what is commonly called golfers Vasculitis. A red or purple rash from my feet up tp my knees which only comes on when I play golf. I have been taking oral hrt (now a low dose called Premique) since I was around 40. I wear support hose prescribed by my doctor which helps a bit, but the condition is worsening. I dread giving up golf as it is my social life as well as my favourite sport.
- Is it bad to take levorphanol tartrate if i have liver damage caused by hep c
I am receiving treatment from the V.A. in Los Angeles, Ca..
Last summer the va started to hint at forcing me to be seen by there pain mngt. team. Also I was to start treatment for my hep c, it was just becomming active. I knew that the interferon would be just a little stressful for aprox; one year so I offered to do there (the pain clinic) plan with a happy heart just after my liver stuff was done. So I went to LA only to find that the liver lab spent just 2 minutes with me to tell me that since I'VE have to wait a new liver drug to be approved I must do the pain clinic. So in six weeks I went from 200mg (5x4 per day) of methidone to 40mg (1 tab x 4 per day), and in just one week it was Oxycodone 40mg x 4 per day to 0. And all of this isij happening my liver gets more serroscised.
More questions for: Magnesium oxide, Vasculitis
You may be interested at these reviews (Write a review):
- Latuda stoped hypoglcymia (1 response)
I have hypoglycemia and have had to be carefull of my sugar intake. Started taking Latuda and now i can eat sugar like most people do
- Avelox with prednisone and nabumetome = disaster
I was prescribed that combination of drugs in January 2013 when I went to my family doctor with a bad chest congestion and painful knees. After starting on the drugs, I got a severely painful neck and thumb and noticed some tingling in my left foot. I took the whole course of the avelox and prednisone, though I discontinued the nabumetome. I kept getting weaker and weaker till I could hardly walk. I ended up in the emergency room and was first diagnosed with Rhabdomyolysis but rushed to a bigger hospital for further diagnosis and treatment. I was close to needing blood, my kidneys were shutting down and I could barely walk. I was so weak! My right hand and left foot went "to sleep" and still haven't woken up. ( as of October 2013)
After many, many tests, they came up with a tentative diagnosis of vasculitis and myositis.
Then I had a kidney biopsy which confirmed the vasculitis and I was immediately treated with chemotherapy -- cytoxin for 6 months.
IAlthough I do feel much better, I am still suffering and taking drugs for the vasculitis and I am told that I may go into remission, but it could flare up again anytime. I am convinced that it was the drug combination that caused all this. I had been feeling great and had a daily walking routine of walking 2 to 5 miles per day, and no other complaints.
The nephrologist did say that while it might be that the vasculitis was drug induced, it didn't matter because I have it and he's treating it and would be doing it this way no matter how I got it.
When I told my family doctor that I thought it was the drug combination that caused my problems, he seemed surprised and really no discussion. I told them to put it in my medical records to NEVER give me a flouroquinolone drug again.
Yesterday when I went for a blood test and urinalysis ( which I was doing biweekly, but now every 6 weeks), it showed that I have a UTI and guess what the family doctor called in a prescription for? Cipro!!!! And he knows I'm still on prednisone and have only 30% kidney function!!!!!!
While I am not a litigious person, this really makes me so upset!!! I don't have the money to try to sue, but if telling my story will help keep unsuspecting people from the horrible damage this has caused, I feel obligrdmtomspeak up. I have had a terrible year. And I'm still not okay. And the drugs 'm taking make me susceptible to other problems. I'm still all puffed up from the prednisone. A couple of weeks ago I decided to try going for walks again, hopefully to lose some of this weight and build up my strength. It is so hard for me and my left foot hurts so bad. My legs feel so heavy it is a real struggle to walk a mile. But at least I can. When I was at my sickest, could barely walk to the bathroom and I could not get up from the toilet without using my arms to pull myself up. I couldn't go up the two steps to get into my house without help. I couldn't go upstairs to my bedroom for months.
- Will axiron affect my epilepsy?
I am an ftm (female to male) transgender and I am a little nervous starting my hormone stage. I was wondering if Axiron will affect my epilepsy.
- Dilantin and interactions
I've taken Dilantin for over 40 years..seizure free for over 30 years..became hypothyroid 10 years ago..B12 deficient approximately 3 years ago and have had a benign arrhythmia for over 30 years. I take magnesium because it seems to hep the arrhythmia and vitamin d because mine is low normal.
More reviews for: Magnesium oxide, Vasculitis
Comments from related studies:
From this study (2 days ago):
have had slightly elevated liver enzymes for 2 years, AST 44, ALT 69
Ys7 on Feb, 10, 2015:
Female 63.had Tt dec2013and is now bothered with cough and lots of phlegm since Christmas.;can't seem to shake it. Blood work now shows elevated liver enzyme. Having symptoms of hypo, when will I be normal again, and what is all this happenings
From this study (3 days ago):
no i am not genetically predisposed for these conditions and all blood tests done with embolism causes have come back negative. majority of effects began with taking Remeron and Prazosin combo. was not diagnosed at all for high blood pressure for Prazosin Rx, actually had normal bp. after getting off Prazosin because of complete disorientation and blackouts, continued on Remeron and continued to get worse and worse depression with thoughts escalating to suicide. doctors have been very difficult in regards to this matter because they have so many clients on this junk and they do not want to lose their kickbacks and holidays from the drug companies but all i hear at the hospitals from other patients is how shitty and how many physical health issues occur while on Remeron/mirtazapine. there needs to be more medical awareness in regards to these products and the research needs to go far beyond "newest is best" mentality. my life is ruined because the prescribing doctor did not even want to monitor as directed for over a year and a half and did not want to heed medically apparent warning signs because it is not spelled out clearly enough that they have to be responsible for their patients conditions. now i run into an issue where my work compensation claim is being denied in regards to the physical side effects despite the recent reports from eHealthMe and FDA because the insurance company claims that there is not enough evidence and no definitive direction from the drug companies. only positive, am now slowly begining to lose weight since extremely hard battle while on remeron/mitazapine including near starving self to stop gaining weight. does anyone have any idea as to how to deal with this with a shortened life span and lifetime Rx for warfarin now demanded on top of possible surgeries and multiple procedures? is there anymore reports or doctors that understand what is going on as i am recieving pressure to continue on again with more antidepresents? what are the official list of "blood dissorders" referred to in the data and medical references about remeron/mirtazapine? is sleep deprivation and nightmares even an authorized/indicated use for Prazosin and if not why are psychiatrists and docs really pushing it for such a use? i am upset but any help with info would be great as i need to know how to deal with my current conditions and i believe the only way to do that is to reach a complete understanding about what went on before i am talked into drugging up a again with medical staff that does not want to acknowledge or educate about side effects and greater potential harm?
Post a new comment OR Read more comments
NOTE: The study is based on active ingredients and brand name. Other drugs that have the same active ingredients (e.g. generic drugs) are NOT considered.
WARNING: Please DO NOT STOP MEDICATIONS without first consulting a physician since doing so could be hazardous to your health.
DISCLAIMER: All material available on eHealthMe.com is for informational purposes only, and is not a substitute for medical advice, diagnosis, or treatment provided by a qualified healthcare provider. All information is observation-only, and has not been supported by scientific studies or clinical trials unless otherwise stated. Different individuals may respond to medication in different ways. Every effort has been made to ensure that all information is accurate, up-to-date, and complete, but no guarantee is made to that effect. The use of the eHealthMe site and its content is at your own risk.
You may report adverse side effects to the FDA at http://www.fda.gov/medwatch/ or 1-800-FDA-1088 (1-800-332-1088).
If you use this eHealthMe study on publication, please acknowledge it with a citation: study title, URL, accessed date.