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Review: could Marijuana cause Endometriosis?

We study 1,028 people who have side effects while taking Marijuana from FDA and social media. Find out below who they are, when they have Endometriosis and more.


Marijuana (latest outcomes from 1,327 users) has active ingredients of marijuana. It is often used in stress and anxiety.


Endometriosis (appearance of endometrial tissue outside the uterus and causing pelvic pain) (latest reports from 11,275 patients) has been reported by people with multiple sclerosis, birth control, rheumatoid arthritis, pain, osteoporosis.

On Sep, 20, 2014: No report is found

Do you have Endometriosis while taking Marijuana?

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Comments from related studies:

  • From this study (8 hours ago):

  • Prescription for marijuana. Replacing it for alcohol. High blood pressure.


  • From this study (5 days ago):

  • Elavil, 25mg @ night stopped an 11 month chronic headache after a head injury, I sustained 1 1/2 years ago.
    Additionally, Neurologist prescribed 100 mg Lyrica for chronic back/nerve pain from moderate/severe spinal injuries, sustained 20+ years earlier. (Crushed/cracked verabrae and 3 intervertebral disc bulges)
    I had been using Ibuprofen daily in moderate to heavy dosage for the last 20+ years. (800+ mg daily B/4 and then continually after recent head injury)
    I was advised to stop/reduce use of Motrin to 1/2 month or less. It is still the best pain relief but have reduced to PRN, perhaps 200 mg alternate days.
    Since treatment with Lyrica I've noticed reduced nerve pain and stopped using Elavil for sake of not feeling so "wrecked" in the mornings. I have also developed a severe sleep apnoea, treated unsuccessfully via CPAP device which is unbearable to use. I have subsequently suffered with depression/mood disorder for 20+ years and am currently un-treated for this long-standing vulnerability which came back with a vengence after the head-injury. I feel irregularity to my heart beat by the end of the day. I feel suicidal and violently angry.


    dutchgirlsamm on Aug, 30, 2014:

    Lyrics is known to cause suicidal thoughts and aggression...its called an adverse reaction.


  • From this study (1 week ago):

  • endogirl on Dec, 13, 2012:

    For those with endo...Mirena DID NOT cause it. You were probably born with it. Also medications cannot cause endometriosis. Please, for yourself and others, do some research and educate yourselves! There are plenty of books on endo. I get very tired of reading misrepresentations of endometriosis and what causes it...this is why it is not taken seriously.


    Trista on Oct, 17, 2012:

    I've always had heavy bleeding until I got the mirena. I was fine for years. Then the last two and a half years of being on the Mirena, I started having extreme pelvic pain. My GYN did a laparoscopy diagnostic and come to find out I have endometriosis. Could the Mirena have caused the endometriosis? I've never had endometriosis and I'm only 27. My husband and I would like to have a kid but we don't want to try since I'm going through treatments and those treatments are a pain to deal with. I'm having severe mood swings, depression ( which I already have but has worsened ), migraines, forgetfulness, and massive weight gain, not including extreme cravings. I had the surgery in April of this year and a new Mirena put in at that time. That's when everything started to get worse. I still have some pelvic pain now that im also on a ten day estrogen tabs for when i get my monthly injection. Im worried that the Mirena caused that endometriosis and i might never be able to get pregnant.
    I was having the signs of bei pregnant with feel nausious by the smell and site of food for over a week. I was tested twice and both came out negative. Please help me in finding out if the Mirena is the cause of this.


    Carrie on Oct, 17, 2012:

    I also used Mirena and about 3 years after having it inserted had to undergo laproscopic surgery to remove the endo. I had a very rough start with the Mirena, for several months I had uncontrolled bleeding and extremely heavy periods. My doctor, (who by the way was the best!)requested I have the Mirena removed and then he do the surgery. Told me it was "textbook" and then gave me several options to treat my endo after the surgery. Including the time consuming Lupo Depron. The best option in his opinion was to try to get pregnant, which was a plan I had anyways. I became pregnant and have yet to have any issues with endo. I've been endo free for almost three years now and have a handsome little boy. I will never go back to Mirena. It was a total nightmare.


    Trista on Oct, 17, 2012:

    When I had the lap surgery the Dr. removed the IUD at that time since I was coming near the five year mark. He recommended to have a new one fitted. The second Mirena I did fine with but the treatments are killing me ( not literally). I really do want to get pregnant but right now in at this time, financially isn't the best. I have read up on endo and I did find that getting pregnant is also the best option for it. I'm talking with my Dr. today about possibly removing the Mirena since this will also be my last treatment for the Lupron Depot.

    I'm glad to hear that you haven't had any endo reoccurring. I'll keep you updated with what the Dr. says and how things go.


    Carrie (28 yrs) on Oct, 17, 2012:

    I really wish you the best. I struggled just trying to get the diagnosis for over a year. I will someday have endo again, it's bound to happen. For now though, it seems to be at bay. I've been put on Lo Estrin 24 to help control it from coming back, if you can remember to take a pill everyday I would suggest you go that route. Mirena was great for the simplicity of not having to take something everyday, but not worth the pain everyday. If you can, it would be better to try to get pregnant sooner rather than later, if the endo gets too overwhelming for your system your chances of naturally getting pregnant will decline rapidly. Best of luck to you!
    Also, I've heard there is a suit against the manufacturers of Mirena due to their not being fully honest about side effects. I'm thinking of looking into it myself.


    brittany on Oct, 24, 2012:

    I had the mirena about 4 years ago and had it in for about 4 months and started to have very bad pelvic pains, i had it taken out and 2 months later i was told that i have endo... this is very disappointing for me cuz i was on 19 at the time. my husband and i have been trying to have a baby since my iud was taken out... and still no luck.. does anyone else feel it was the mirena that caused the endo? also visit and the mirena iud is listed on there... all the symptons they talk about are symtpons of the endo...


    samantha on Jan, 23, 2013:

    hey i had the IUD back in 2008, my dr said the first one fell out an they put a second one in an i had problems with that. had it taking out in 2009 an was told that it was put in wrong an me an my husband cant get pregant right now an we have been trying for the past 4 year. so i think the IUD has caused problems with me.


    Missesllj on Nov, 27, 2013:

    I am 21 and I had my IUD put in in July of 2012 and had problems pop up after. I was getting extremely bad cramps that would take me to the ground sex became unbearable and the pain made me so sick I couldn't eat anymore. Finally went to the doctor and the ultrasound showed I had 8 ovarian cysts so I was put on meds for a month and went back with little relief they then ordered a laparoscopy which showed endometriosis keep in mind I had never had an ovarian cyst before getting the mirena nor any problems in that area. I was told that it was genetic blah it's not I have no family history of this I've done my family research. I think it's odd how I've read hundreds of posts of women being diagnosed with endometriosis after having a mirena put in. And for endogirl maybe you should do your research there is ingredients in medication and lots of other products (deodorant being one) that cause something called reproductive toxicity which is a cause of endometriosis. There's a lot more to endometriosis than are in the books so like I said do your research before you tell these people they are wrong.


    shell on Aug, 26, 2014:

    I am 28 and was diagnosed with endometriosis in 2010; two years after having the Mirena IUD removed through laproscopic surgery. Why the surgery you ask? Two weeks after the IUD was inserted it punctured through my uterus. I was very nervous about all of the side effects to the Mirena so i checked for the string daily and one day they just weren't there. I went to the Dr. and had an X-ray revealing the IUD was outside the uterus and somewhere by the intestines. Because of its placement and position i needed to have emergency surgery. They were afraid it would puncture my intestines and cause further problems. So with two children and husband at home i went in for surgery. All went well and I recovered as expected. I thought that was it, all good now. WRONG! Over the next two years I had more than normal periods, with more bleeding, more pain, and lasting 2-3 days longer. Pain with intercourse was frequent and I eventually developed cysts. At one time there was a rather large chocolate cyst that needed to be removed. This meant back in for surgery. After this surgery they told me they got the cyst but had to take that ovary and tube as well because it was too damaged. Then the even worse have stage 3 endometriosis. I've been dealing ok with this now, they removed as much as safely possible but I just want everyone to know I never had any kind of reproductive issue ever. No pain, at least not more than normal, and never had endometriosis before this. So yes I do blame the Mirena IUD and wish I would have been less naive and not said, "this won't happen to me."


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