Lupron and high blood pressure

I was given lupron depot 5 years ago (2004) for endometriosis & adenomyosis . I researched the side effects and upon learning them I didn't want to take the shot. I suffer from multiple back problems, and the bone loss scared me. I voiced my concerns with my doctor at that time. He told me he knew better (he didn't want to perform a hysterectomy) and that he was giving me the shot. It has been a nightmare since. The side effects were terrible, the worst was the severe mood swings. Lupron depot changed who I was. I no longer was the happy carefree person I was. I was constantly angry and because of this drug I developed high blood pressure. This has not improved in 5 years. (I also gained weight from the shot and it took me 4 years after the last shot to finally lose all that weight.) I do not recommend any woman to take this shot. Do not let your doctor talk you or bully you into it. They only care about the money not you!!!!!!!

I'm so sick with all the side effects just was released from the er for high blood pressure now great! it has been 1 month since my 5th and final shot how much longer until these side effects go away?

I just went in for my second shot of Lupron (out of a series of 6) for treatment of stage IV endometriosis. The most noticeable side effect I experienced was during my first menstrual cycle after my first dose of Lupron. I had never experienced menstrual pain or cramping (even though I had advanced endometriosis) until after Lupron. I have a fairly high pain tolerance and yet the cramping for the first 2 days of my period were almost debilitating. I had extremely heavy bleeding and have had spotting daily ever since (app.18 days). I have gained about 3 pounds because I have no energy at all. I'm usually active and work out 4-5 times a week but by the time I get off work, I'm too fatigued to do so (hence the weight gain I guess). I have hot flashes and night sweats all the time. The most recent side effect is high blood pressure. I have never had high blood pressure in my life (I'm a healthy 25-year-old woman) and when I went in for my 2nd Lupron shot today, they told me I all of a sudden do. I don't seem to have mood swings but do feel depressed and sometimes more anxious than normal. I have experienced a decreased interest in sex as well.

I am in month 4 of a 4 month Lupron shot that my doctor gave to prepare for surgery. I was told I might get hot flashes, loss of libido, increased urinary symptoms for a few weeks. No one said anything and there was absolutely nothing in all the drug leaflets they gave me that would have prepared me for the the horror story that my life was about to become. As if having cancer was not bad enough.Since day 2 I have suffered so many bad side effects that I have lost count. The worst is insomnia and nothing has helped including high doses of Ambien. They suggested Lunesta but my health insurance company balked and even if they had said yes, my co-payment would be unaffordable. This stuff is more expensive than gold. I am exhausted all the time. I have terrible memory problems that are so bad that I can be talking to some I know really well and not remember their name. I am unable to concentrate on anything, my mood swings are unbelievable, I feel mentally disoriented and dissociated all the time, high blood pressure, racing pulse, high blood sugar, hot flashes, raging night sweats, dizziness, bad balance. The side effects that I can handle include nausea, headaches, diarrhea, joint and muscle pain. I am supposed to be on Lupron for 2 years. The only difference I see with my Lupron experience and others here is that my gender is MALE and I have early stage prostate cancer. Being male, my other serious Lupron side effect is complete impotence which is going to go on for a long while due to the radiation. I had radioactive seed implants into my prostate gland done a week ago and I have to follow this with 5 weeks of beam radiation. Lupron seems to be an equal opportunity drug. Lupron has messed me up so badly that for the past 5 weeks I have been off work on disability status with no chance of going back for at least a month and my Dr thinks that may be optimistic. No one seems to know how long it will take to get back to some kind of normal. I just could not function at work and ended up in my doctors office having a complete emotional meltdown. I would caution anyone, male or female, to consider Lupron very carefully before having it.

I see Lupron as a necessary evil. I am waiting for surgery in 2 weeks and Lupron has stopped me from menstruating which is a good thing. That is about the only good thing about Lupron. I haven't gained the weight people are talking about but am working out a lot. My symptoms are some night sweats but the dizziness, increased blood pressure and blood sugar and general achiness are the worst part of it. I also get headaches that come and go more after an injection; I have had three - one each month. Thankfully, I had my last one this week. This drug causes your body to try to speed up since it is depressing some of its functions which apparently is the cause of the high blood pressure. If there are any possible alternatives, I would go with that rather than lupron. I have run out of other medical options so only had Lupron until my hysterectomy.

I had 2 lupron shots back in April and May and it was the worst decision of my life. I now have SEVERE panic attacks, depression and loss of appetite. I was a very healty 33 year old woman and very active and now all I want to do is stay in bed. I was NEVER informed by my doctor of any side effects other than I MIGHT get a little moodier (angry) easier. That never happened. For 2 months straight all I did was cry. I would wake up crying and go to bed crying. I have never had any past experience with depression and I have already seen a psychiatrist and 4 other doctors. I finally saw a new OBGYN and she informed me that the 2nd shot that I received went straight to my head and it messed with the chemicals in my brain. I am a wreck. I have no energy and it's all I can do to just get out of bed and go to work. Had I known about ANY of these side effects, I would have NEVER taken this drug. This drug needs to be banned completely and thrown in the trash can before any other woman goes thru this. I was on the verge of being suicidal. I am a Christian woman and would never harm myself but the thoughts were always there. I would wake up with a severe panic attack and they would come all during the day. The doctor that originally gave me the shots told me I had psychological issues and HE HIMSELF called and got me an appointment with a psychiatrist. Ladies, we are not crazy. These are real symptoms and it is all because of these shots. It messes with the chemicals in your brain. And had I know that, I would have said HECK NO to them. My endometriosis is much more tolerable than these stupid, insane shots. Please do not take them if at all possible. I do not want one more woman to go thru what I have been through and still going through. I now am on anti depressants to try to get the chemicals in my brain back to where they should be. I just hope and trust in the Lord that I will eventually get through this.

After my 2nd monthly shot of Lupron I experienced heart palpitations and high blood pressure. I felt as though my heart were going to burst while I was laying in bed trying to fall asleep. I saw a cardiologist who prescribed a BP med. Now I am on 1 medication to combat the side effects of another. I am due for my 3rd shot. I am buying time until my hysterectomy. I am worried that this 3rd shot will be stronger and worse than the first 2. I do not have any other worrisome side effects.

Hi...I'm glad I found this sight! I don't recommend Lupron; I think its bad side effects outweigh its good ones.

I only took one 3-month shot of Lupron in July of '07. I had horrible hot flashes...which I was told to expect, but the vaginal dryness, lack of sex drive, weight gain, breast changes, vaginal dysfunction, and, I believe the high blood pressure I now have is associated with this drug. I actually started looking for side effects online because my blood pressure has been elevated ever since taking Lupron. It is now January '08, and I still don't feel normal!

I took one injection of Lupron for fibroids in Nov. 2001. It totally changed my life, I am no longer the same person I was before. It started with severe migraine headaches for 14 days straight and attacks of nausea, lack of appetite. I used to have a strong stomach - now I was very easily nauseated. I never went for the second shot. I began to have panic attacks regularly (I had not had them for over 20 yrs). I was tired all the time, and a person who used to work out at the gym 5 days a week - eventually I quit. Now I just walk. I feel about 65 yrs old (I am just 49). I look old, my face began to droop, my hair thinned. I had bouts of depression coupled with general anxiety. My migraines worsened. My sex drive dropped to zero, I feel almost "sexless". I used to be confident, now I was afraid of everything. I now suffer from irritable bowel syndrome - with bouts of diarrhea, bloating and severe gas pains. I have trouble eating sometimes.. I have had all the tests and no one can find anything wrong with me,and none of the doctors think all these problems are due to Lupron. But, I know - I was NOT like this before Lupron. It ruined my life. I just wish my doctor would have informed me of all the terrible side effects - she only told me about hot flashes. I looked into suing her for malpractice but the lawyers said they could not build a case with no real medical evidence that my symptoms are caused by Lupron. I just wish I had known then what I know now. I tell everyone - NEVER take Lupron. Six years later and I still feel like this. Oh what I wouldn't give to have not taken that drug.

I have not taken Lupron. In fact, I refused to take it at my doctor's insistence. I am a healthy 45 year old woman - why would I give that up for a temporary fix (6 months at most) for my endometriosis when I may have other options?

I don't want to trade my low blood pressure, healthy body weight, healthy bones, ability to sleep, clear skin, normal bowel movements, lack of severe migraines and lack of irritability for lack of endo pain.

I do not discount the endo pain - it can be crippling - but so is this drug! Everyone must make their own decision regarding whether or not to take Lupron but please, please do your research. Most doctors don't let you know that you have options. Call the Endometriosis Organization and ask for a specialist in your area. Endo is a little-known and often misunderstood disease. Find yourself a surgeon with a great deal of experience with endo - NOT an OB with a great deal of experience delivering babies.

It really upsets me to see so many women feel that they have to pay this price to relieve the pain. I am going to an endo specialist for a second opinion in a couple of weeks. I don’t know what he’ll say about my case but I am pretty sure the answer won’t be Lupron.

I am not usually a person who senses a doctor or a drug company is unethical, but remember, there will be no greater advocate for your health than yourself! Educate yourself, and ask your doctor lots of questions. If your doctor gives you a hard time – find another one. It’s your body and you have to live with the consequences.

Lupron is terrible! I was given lupron after my lap which discovered endometriosis. I had my second injection last week. My pelvic pain is still here and now the Lupron side effects are killing me. I have insomnia, restlessness, bad mood swings, back hurts all the time, fatigue all the time, depression, headaches, and awful HOT FLASHES. I was not given other options but to take this poison. If I had done my research I would have said hell no to Lupron. It's all about the money...Dr's and pharmacy companies are making the big bucks while most of us suffer. Oh yes, and my blood pressure, which is normally low (110/60) is now up to 150/100. I'm not thinking this is too great for my health. And another sad thing is that the long term effects are not really known. I WILL NOT take another injection. I would rather take my regular endo pain over this in a heartbeat. Don't let them fool you.......Lupron is a VERY BAD thing. Anyone who is thinking about....do you research and think long and hard . Is it worth it? I don't think so...
Kelly

High Blood Pressure, hot flashes, no sleep

My sister is currently on her 5th month of the Lupron shot. She has had serious, and unexplained complications that her doctors have been dissmissing as not results from the shot. She lost 45 lbs in less than 3 months, has high blood pressure, and recently blackouts. Her first resulted in only stitches, but the second time she was behind the wheel, and almost died. Now the doctors have banned her from driving, and are sending her to see Nuerologist, and Cardiologist for exams. They still say this is not a result of Lupron. Our family tends to dissagree.

53 year old, runner, given shot for fibroids,Day after 1st shot (30 day) side effects started: High blood pressure, racing heart, shaky hands, flushing. Had these problems for a couple of days, then started with chest pain, chest heaviness, shoulder and neck pain feeling like I couldn't breath, pounding heart, barely able to make it up the stairs in my house. Ended up in the ER from the severe chest pain - all tests were normal.
additional side effects two days later - blurry vision at times, tingling in hands and feet, occasionally spreading up to my head, insomnia, pounding feeling in my chest, another trip to the ER - again all tests normal. Now on top of all the above, I am having severe indigestion and feel like I have a large lump in my throat and have a hard time swallowing. I still have 2 weeks left. Hope it all goes away soon - also have been bleeding for about 10 days - What a nightmare!!!