Review: could Marijuana cause Arthritis - osteoarthritis (Osteoarthritis)?
Summary: there is no Arthritis - osteoarthritis reported by people who take Marijuana yet.
We study 1,072 people who have side effects while taking Marijuana from FDA and social media. Find out below who they are, when they have Arthritis - osteoarthritis and more.
You are not alone: join a mobile support group for people who take Marijuana and have Arthritis - osteoarthritis >>>
Marijuana has active ingredients of marijuana. It is often used in stress and anxiety. (latest outcomes from 1,372 Marijuana users)
Arthritis - osteoarthritis
Arthritis - osteoarthritis (joint disease caused by cartilage loss in a joint) has been reported by people with osteoporosis, osteopenia, rheumatoid arthritis, high blood pressure, pain. (latest reports from 33,243 Arthritis - osteoarthritis patients)
On Jan, 14, 2015: No report is found
Do you have Arthritis - Osteoarthritis while taking Marijuana?
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- Can smoking marijuana help episcleritis
recurrent episcleritis, have not respondent well to steroid drops,nor oral steroids.
- Can i get sporotrichosis from smoking or handling marijuana
1 1/2 years ago i had a stomach bleed. Hemroids. Alchoholism. Recreatoinal drugs. Recently i have been working in horse barns chicken coops and an organic marijuana farm. Many plant cuttings started dying very fast due to fungus gnat infestation. After handling thousands of dead dying and rotting plants in late June i accumulated several small sores that appeared to be staphylococci. Treated for mrsa with pills and topical cream. Was also having urinary track infection symptoms as well as irritated hemroidal rectum. Suggested Epsom salt baths and drink for detox and stool loosening. Within 1 hour suffered from magnesium sulfate toxicity. ER treated with munopriocin and ciproflaxin antibiotics @15,000 milligrams. Finger check in anus for prostate problems. Hurt very bad and finger was not in anus more than 1 inch. 3 days later staff symptoms were back and more aggressive. This time traveling my lympnatic track
Ulcerated lesions behind both ears chest shoulder neck forehead forearms . Lesions come fast and leave very slowly. They tingle itch swell And leak off and on thruout the day. Scarringvery badly. 8 months And still happening. No alcohol for 6 + months. Doctors will not take very gross samples from me and their biopsies keep turning up negative for bacteria and fungal. What is this?
- I have been told by my gastroenterologist that i have gastroparesis, what are my treatment options, if any?
I've had a CT scan and a Gastric Emptying study completed. My stomach is only 35% emptied after 4 hours, it should be at least 90% empty at that point. I have a colonoscopy and esophagealendoscopy scheduled for the first week of the year. What are my treatment options at this point?
- Does anyone experience heart palpitations causedby their acid reflux ?
I have had acid reflux/Gerd for 4 years + Was not believed that symptoms were real for a while as had no heartburn and a diagnosis of Fibromyalgia which even now some medics think is imaginary...it's NOT!!! Following a demeester score of 45 ( very high confirmation of acid reflux) and discovery of a large hiatal hernia, ( a classic physical cause of acid reflux) I had hernia repair operation and LINX anti reflux surgery. Throughout the four years a major symptom of my acid reflux were heart palpatations. They started at the same time I started with reflux and cleared up after the surgery. I have been reflux free palpitation free and antacid free for four months. then I was put on Gabapentin for back spasm and the reflux returned along with the palpitations. Medics keep insisting this is just anxiety yet eat a food that gives me reflux also starts the palps which is the indicator of the reflux as I do not have heartburn. Comes on when relaxing and eating watching tv ( no anxiety present) and when I am sleeping peacefully ( no anxiety present) my heart wakes me up and fires off into tachycardia. Recently a doctor has said it is now known that acid reflux irritates the nerves in the solar plexus area and that triggers the palps. Anyone else experienced this? Are there any studies on it at all? Thanks all.
- Could smoking marijuana once cause retinal detachment? after smoking a small amount of mj, my retina detached and i ended up having emergency surgery to mend it.
I had had laser surgery, cataract surgery much earlier--all successful. Members of my family have glaucoma and so do I. After hearing that marijuana might ease the glaucoma, I smoked one time. That night, my retina began to detach. Is there any causal relationship between the marijuana and the retinal detachment?
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- Good effect of marijunana for hematuria
i had hematuria sence 3 years,i had done lots of tests like radiology,cystoscopy,kidney biopsy and many more,but all reports were normal,so after that i started a new type of thearpy that was HOMEOPATHY.but there was no results,but suddenly in party i has smoked weed sence that time there was no blood in my urine,marijuana was a very big medicine for me.and now i dont have any problem again in my urine,5 months had happend but still now no blood
- Pulmonary arterial hypertension and marijuana
Marijuana does not cause Pulmonary arterial hypertension, instead it treats it. This study proves that the indigenous cannabinoid, anandamide, lowered aldosterone levels, and therefore would lower blood pressure (http://www.odon.uba.ar/uacad/fisiologia/docs/nuevos/expression.pdf).
For more than 15 years, no blood pressure medications would keep my blood pressure down. I would be on two medications, yet hospitalized with a pressure of 200/130 when I stopped treating my illness with cannabis. Now, I am on no blood pressure meds, and keep my pressure down around 130/78. I would have had a stroke years ago without it.
- Pruritus ani. and marijuana (1 response)
i just got popped for smoking weed on a drug test 2 weeks ago. OF COURSE i was crushed by this news,BUT,i think not smoking the last 2 weeks has CURED my pruritus ani. I suffered and i mean suffered with this the last 2 years and tried giving up everything i thought might have caused this. Certain foods,beer,diet soda to no prevail. I havent felt this good down there in over 3 years!!!! If i knew that was what was causing this,i would of quit years ago and never got popped in the first place!!!! And yes,i would rather give up smoking weed then feel what i felt the last few years.
- 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.
- Sepsis hallucinations misdiagnosed
I was admitted to the hospital at 10 p.m., with a total bowel blockage caused by scar-tissue adhesions. I had first gone to the ER at 3 a.m. that morning, but the ER doc misdiagnosed my condition as constipation. I was in extreme pain and also too weak to tell my husband when he first came home that I needed to return to the ER. By the time I returned, I became violently nauseated, and vomited repeatedly. Then a gastro-nasal tube was forced down my nose and into my stomach. I began hallucinating at approximately 5 p.m. the following day. I did not realize I was hallucinating, and thought my experiences were real. Some were quite coherent, such as believing there was a book sitting on table at home with a photo on the front showing a sculpture in white marble of a woman's hands holding the Bible, with barbed wire wrapped around her hands. I thought the sculpture had won the Nobel prize, and the book was the biography of the sculptor, whose mother had gone to extraordinary lengths to keep him safe from the Nazis. Some may actually have occurred during dreams, and were wildly improbable, but I don't recall ever going to sleep. At one point, I thought I was at a rest stop on the NJ turnpike, and saw the Nobel-winning sculptor there, working on a wood sculpture. The sculptor turned out to be the maintenance man on the hospital floor. I pulled out the naso-gastral tube three times, but was unaware that I had done so, although I do remember believing that I was buried beneath peat moss and feeling suffocated as I clawed my way out. I also thought I was at a party being given by a law firm which had sold its building to a school for gifted children, but I (also a lawyer) had been deposited there by my nurse and her boyfriend, who were supposed to have taken me to the OR. Some scenes from a book I had been reading made their way into my delusions, which were so real to me that I actually called some of the people involved later on and asked if the events had really happened. The hallucinations began before surgery and continued afterward. When I awoke from anesthesia, I thought the hospital staff was painting the doors to my upstairs bathroom, a project I'd been involved with before the blockage struck. I asked them how they knew what colors to use. They thought I was joking, and confirmed that they had gotten the colors right. Finally a neurologist was summoned, and I told her I was on the passenger ramp at La Guardia airport (instead of in a hospital in NC), and that I'd been born in Havana, Cuba (instead of Baltimore, MD.) I believed myself to be a member of the ruling party in Cuba (pre-Castro) and during an outdoor ceremony, an earthquake had struck, causing ancient monuments to come tumbling down. Later, I was bobbing in harbor waters near a huge ocean liner, with plastic bottles and other detritus floating by. The foregoing are only a small sample of the multitude of hallucinations. Occasionally, I was only an observer of astonishing events, but usually I was a participant. I recognized my husband and friends, but told them about many of these events, believing they had happened. The neurologist diagnosed clonazepam withdrawal. My other doctors later said this was unlikely, as I took clonazepam in small amounts on an erratic schedule, and was not dependent on the drug, although my prescription called for 3 mg. daily. Physician friends said my symptoms were more likely the result of sepsis. I did contract a urinary-tract infection from the catheter, and was being given antibiotics. Additionally, the nature of my underlying condition, and the delay in diagnosis and treatment, may have contributed to the sepsis. Hallucinations occur in only a very small percentage of sepsis sufferers, and in only a small percentage of those withdrawing suddenly from clonazepam. However, I do fit the profile of those who do experience hallucinations with sepsis, being female and aged 62 at the time of this description. After the three-day period, I returned to normal, although believing that my hallucinations had been real persisted for some days afterward. I recovered quickly from the surgery, although the pain persisted for a while, and I was walking easily (dragging my IV with me) through the hospital halls. This was the ONLY symptom I had. Not all the hallucinations were unpleasant -- in fact, they were highly interesting -- but they were incredibly complex. I still remember all the details, better than I remember what actually happened yesterday. Except for the urinary-tract infection, I had no other adverse effects from hospitalization -- no fever, chills, nausea, sweating, headaches, trembling or anything of that kind. The bowel blockage and the surgery were of course not fun, but in a way the hallucinations were fascinating. My own feeling, and that of the doctors who know me and my medical issues, is that my experiences were caused by sepsis, not clonazepam withdrawal, and the antibiotics I was given are probably what saved me.
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Comments from related studies:
From this study (2 weeks ago):
I have been on this drug for 2 years now at least straight with the add-back therapy (Estrace 1MG and Apo-Medroxy 2.5 MG) that is supposed to protect me from osteoporosis allowing me to stay on the drug lupron longer then a year as per a new study my gynecologist had recommended for me. This summer have found out I now have a deteriorated disk in my back,lost a tooth and now just today (Dec. 29, 2014) have a tooth that is after cracking for no reason!!!! I ate nothing hard! My bone density is showing a risk for osteoporosis and I am only 40! On the positive side it has reduced my pain so I have a quality of life instead of pain in my abdomen 24/7 but now I have permanent damage to my back and don't have the money to repair my tooth so could have to get another pulled, to add to it all!It is my jaw teeth so now how will i eat! More studies have to go into this drug!
Hyperacusis woman on Jan, 1, 2015:
If you are discussing temazepam, then, yes, temazepam is known to cause bruxism during sleep. I too had a cracked tooth because of temazepam. I had to get a post and a cap (about $5,000) to replace a virgin tooth (i.e., no previous damage). If you use temazepam, I urge you to get a mouth guard made by a dentist. Regarding the back, I had an MRI showing two damaged back vertebrae after being on temazepam for three years. I don't know if temazepam played a role. I'm a woman in a profession who is in her mid-to-late 40s and who was physically fit and active. I was on temazepam for 4 years total. I don't recommend the drug, as it made me depressed and irritable. (I have no history of psych problems; I am cursed with hyperacusis.)
From this study (4 weeks ago):
Ihave multiple lipoma all over tha body andmost of them pains when toched or pressed,I Suffer mood swings very often. There were no reasons but enjoment and now I have stoped it but I smoke.
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