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User Reviews for Eligard to treat Prostate Cancer

Eligard has an average rating of 4.4 out of 10 from a total of 29 ratings for the treatment of Prostate Cancer. 21% of reviewers reported a positive experience, while 45% reported a negative experience.

Eligard rating summary

4.4/10 average rating

29 ratings from 31 user reviews.

Compare all 59 medications used in the treatment of Prostate Cancer.

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Reviews for Eligard

Bill · May 21, 2020

“Massive radical prostrate surgery 1997. Clear of the return of cancer until 2016, low PSA of 18 when discovered at my annual physical. No radiation, only Eligard every six months. Here it is 2020 and I am 86 years of age. Only side effects are increase in weight (15 pounds), low energy level, and increased breast size. Never hot flashes or sweating. COVID-19 has keep my wife and I house bound for the past 3 months and we enjoy life in states of happiness, bliss and joy. If one lives long enough, prostrate cancer will eventually put you under. Too many symptoms to make a doctor's appointment. When I think it is cancer of the wrist, it's arthritis. When I think it's cancer of lumbar region, it's vertebrae disks. So why think you're going to live forever. Enjoy the love your wife, children and friends offer and learn to enjoy how cancer progresses during the last phase of life. My wife has NEVER heard me complain.”

10 / 10
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Wally · Taken for less than 1 month · January 9, 2020

“Have had one month injection of Eligard and will not be taking another. Side effects including hot flashes, night sweats, fatigue, joint pains, mood swings, memory loss - I get the lot. Worst decision I ever made and hope the effects wear off ASAP. I would rather take my chances than be half the person I am now. Reading other comments where there seems to be no ending to the side effects gives me little hope for a reprieve. Oncologist gave me no impression I would be suffering like this. Just "this is the standard treatment" - it does not cure the disease just supposedly slows it. Personally I would rather have less time and good quality of life.”

3 / 10
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Peartree · Taken for 1 to 6 months · December 19, 2019

“I am 68 years old. Had 6 mo. injection August 2018. Dr. told me hot flashes and night sweats were the side effects. That I could handle. What I could not handle was the loss of cognitive functions, mood swings, loss of muscle mass, weight gain, thoughts of suicide, total ED, shrunken penis and testicles. It has destroyed my life. I have still not recovered all of the cognitive functions I lost, can not get rid of the extra weight and to top it all off, my cancer was not to the point I needed the hormone. Eligard may have saved lives, but to me the treatment has destroyed my quality of life.”

1 / 10
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Bart · Taken for 1 to 6 months · May 2, 2020

“Diagnosed with prostate cancer in April 2019, had a 6 month Lupron shot in May followed by 45 radiation treatments ending in early September. Went on vacation and able to do 2-3 mile hikes over rough terrain with only a little fatigue. Went in for second shot early November and they changed me to Eligard. They said it was virtually the same product. Within 2 weeks I developed intense pain in my hips that has not gone away. Can hardly walk to the mailbox any longer due to the pain. Dealing with mood swings, minor depression, trouble sleeping and have gained 30 pounds. Due to go back next Wednesday for another 6 month Eligard shot. Not going to happen.”

1 / 10
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Rob · February 25, 2021

“Got the results back, in September 2020 had a biopsy (thanks for the delay covid) came back with Gleeson score of 9 and Grade 5! They tried to operate but too much scar tissue. Next was the oncologist appointment who said we need to do something now and said eligard should stop it growing . What they didn't say was that I would put weight on, the night sweats make you put covers on, take covers of all night, Getting up to pee up to 9 times a night, Feeling lethargic, Dark thoughts and mood swings, An emotional wreck. Went to the gp who put me on anti depression tablets which have amplified my emotional state.... told the wife tonight I'm not taking any more anti depressants, not doing eligard and not going to a planning day. I want to go out on my terms feeling like myself not juiced up on this rubbish. Facts are I could have some good years left without medication or go on feeling wound up and unintentionally pushing away those that care.”

1 / 10
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Steelie · Taken for 1 to 6 months · October 26, 2020

“I was given a six-month injection on Eligard 45mg, then 3 days later I had a CV event on me in the emergency room. Other side effect that Eligard has given me is I've had bone pain, severe neuropathy, night sweats, night terrors, brain fog, confusion, anxiety and anger.”

1 / 10
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pofoto · Taken for 2 to 5 years · October 25, 2020

“I was diagnosed with prostate cancer in 2014 at 64 years old. My doctor said my best option for getting rid of the cancer was to have it removed. I went through the surgery in August 2014, but the cancer was not gone. I had 38 radiation treatments in 2015, and that kept my PSA low for two years. It went up to 1.0, and the doctor started giving me Eligard injections every 3 months beginning in 2018. I have severe depression with dark thoughts concerning my death eventually from this cancer. I also have weight gain, and no sexual desires at all. I have no toleranceor patience and it makes me very irritable. I must admit it works as it has kept my PSA below 1.0 for the last two years! I don't think I will take it much longer. My doctor is saying they are looking for a different treatment soon. I have no idea what that will be. It has taken all the joy of life out of me and I am not interested in almost anything...”

5 / 10
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Frequently asked questions

Steve · Taken for 1 to 6 months · January 29, 2021

“My side effects from Eligard is extreme bone pain, joint pain, testicular pain, my penis shriveled up like I had jumped in ice water and stayed icy cold for several days, night sweats, night terrors, nightmares, brain fog. I had a CV event 3 days after wound up in the emergency room with extreme difficulty and pain urinating, especially at night. According to the manufacturer this is supposed to be used for palliative care Well I guess they don't know the meaning of palliative care I wish I had never started this treatment”

1 / 10
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Jean · Taken for 1 to 2 years · April 24, 2019

“Been taking Eligard for 5 X every 3 months, just over a year. Prostate out 10 years ago. Radiation 45x about 6 years ago. Eligard effective at reducing PSA. Occasional hot flashes. Tire easily. Often light headed. Little tolerance for BS. More headaches. Breast enlargement. Thinking about stopping use.”

4 / 10
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Screw cancer · Taken for 6 months to 1 year · October 13, 2020

“Husband got Eligard shot to minimize size of prostate to prepare for radiation with 6 month follow up. When he returned the cancer had spread to his bones and PSA went from 32 to 182 in those 6 months with no additional PSA tests given. The shot was ineffective and we were not informed that it could metastasis to other body parts giving us a choice of a different treatment that would not limit his life.... Demand monthly PSAs!!!”

1 / 10
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Tom 627 · Taken for 1 to 6 months · May 25, 2019

“Been on Eligard for two months and it has taken all the joy out of life. There will be no second injection. My life expectancy is better with cancer than with Eligard and I'm fighting such dark thoughts almost everyday, afraid I'm going to hurt someone, the mood swings are unpredictable and scary. Sex is becoming near impossable all the time.”

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Dave · Taken for 6 months to 1 year · September 3, 2018

“I was prescribed Eligard by an oncologist due to a suspicion of prostate cancer. I was told my PSA of 80 was almost a certain indication of prostate cancer. Seven months ago, in February I was given a three month injection.. Within an hour I was nauseated. I vomited for three hours. After that the effects of Eligard began to take effect. Hot flashes going from sweating to cold within minutes loss of libido for myself, no sexual satisfaction for my wife. Chest constriction Reduced ability to handle stress Disrupted sleep due to fluctuating temperature. Final comment: I conclude that no man would ever prescribe Eligard to another man if he had taken it himself. It is not a cure for prostate cancer, and it affected my life so negatively, I would never take it again, even if I knew I had cancer, which I don’t. I am writing to the Chief Medical Officer of my province that this drug is a poor choice for any purpose.”

3 / 10
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:/ · Taken for 2 to 5 years · June 28, 2016

“I am the wife of a man currently taking Eligard. I have to say it has worked to keep the prostate cancer from spreading. Which is absolutely wonderful. However it has caused a lot of other problems which has effected both of us. He has absolutely no sexual desire, he has developed which appears to be breast, his penis has become inverted and his testicles have decreased in size. His muscle mass has decreased as well and the weight gain is mostly in his belly. I can only hope that he will regain his man hood if and when he is taken off this medication.”

10 / 10
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illini71 · Taken for 6 months to 1 year · October 30, 2019

“Received an 6-month injection of Eliguard. Approaching 8 months since injection and I am still having several HOT FLASHES every day and night. Unfortunately, there is not a remedy that will bring an end to the episodes.”

2 / 10
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Bill Bunch · Taken for 1 to 2 years · November 6, 2016

“I must say if I only knew what this medication was going to do to me I would of never taken it. At the age of 61 this medication has destroyed my life. After each injection it caused deeper and deeper depression. What at one time brought joy to my life is gone. There is no since of any type of sexuality at all. Nothing brings joy to ones life. after each shot it just makes it worse. The hot flashes are so severe I will have to change my work shirt a couple of times a day. I will soak a shirt with in minuets. One has to remember that the Eligard will get rid of all your hormones. we are not made to run that way and there is no support that will help you deal with that or tell you what to expect. You are no longer male but not female either.”

4 / 10
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Patient 007 · July 24, 2021

“I just got my 3rd shot of Eligard. Hard to say exact side effects, because I also have end stage COPD. I haven't got a PSA yet, prior to Eligard, it was 7, then 17, then 24. Due to Covid...I put off seeing an Oncologist for 7 months. I got both Moderna vacs in March...I started Radiation in April and finished on June 9. It seems each shot of Eligard is getting a bit worse. This last one hurt and burned longer.. a minor issue. Hot Flashes seem more frequent. I too go to bathroom about 9 or 10 times a nite...every 1 to 1.5 hours, but that was happening before Eligard. I am dizzy a lot...and I don't have much energy (I used to be quite active). I am 66 years old. My cancer rated as Stage 3...there were tumors on 8 of 12 biopsy samples. Surgery wasn't an option since scans showed it may have spread to lymph nodes. I will update this (if possible) with my PSA score this September. Good luck to everyone. I can't recommend Eligard or condemn it as of this writing.”

5 / 10
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Anonymous · January 3, 2010

“I was given two injections of Elgard before beginning radiation therapy. Following the 48 radiation treatments, I am still being monitored by my oncologist and urologist. My last PSA was 0.01. The side effects of hot flashes, lethargy, and muscle weakness are where I am today, although at my age, 79, I can't complain. The first of the injections was in April of 2008 and the second in August. Radiation began in early September 2008 and ended at end of October. It was determined that I am not a candidate for Androgel as there is a possibility of developing cancer again. So, as you read from the preceding paragraph, I'm lucky to have passed my first year without problems.”

6 / 10
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Bikefox · Taken for 6 months to 1 year · October 16, 2021

“I was diagnosed with prostate cancer around Thanksgiving 2020 and given a one month dose of Eligard about 2 months later. Then two more 6 month hormone shots of Eligard. I have also had SBRT and brachytherapy. So while it is difficult to assign the side effects I am experiencing to the Eligard alone, I am affected by nearly all its known side effects. I have zero libido, 4 or 5 hot flashes per day, major loss of strength and energy, genital shrinkage, body hair loss, weight gain, frequent urination at night, some short term memory loss, mood changes, apathy, and increased frequency of bowel movements. I have trouble carrying groceries up the stairs where I live now because of my loss of strength. I have continued to exercise and I take calcium, vitamin D, and multi-vitamin supplements, but I am still getting progressively weaker. The good news is my PSA is around zero now, and if it doesn’t increase I won’t have to get another Eligard injection when this last one wears off.”

6 / 10
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BarryL · December 7, 2011

“I was given my first injection with Eligard on December 1st 2010. I started to have bone pain a little before this and a PSA of 116. It took control in about 2 days and the pain went. As I decided to wait until the pain returned (to see how long it would last) I had to have another one 6 1/2 months later. My PSA dropped to 0.17 the first time and 2.6 the second (where it is now). I will take a 3rd one in 5 months time and see if it goes beyond the 4 months for the 30mg to have effect. The date is 8th December 2011 and the 3rd one is due in March 2012.”

8 / 10
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What to Do? · Taken for 1 to 2 years · April 1, 2022

“My husband was diagnosed with prostate cancer 2 years ago. Underwent surgery to have prostate removed as well as lymph nodes and some cancer that was on his bladder. He started the Eligard injections every 3 to 4 months since. His PSA levels have remained at a 1.0 until recently. A friend suggest he take a multi vitamin of Quercetin, zinc, stinging nettle root, Vitamin C and D3. He has been taking it for 3 weeks and just went back in for another injection. His PSA was 0 but yet they still gave him the injection. If his PSA is 0 why would he need another injection. He continues to suffer from all the same side effects of night sweats, frequent urination, mood swings, depression, and loss of memory. I want him to stop the shots but wondering if anyone else has quit taking the shots with a PSA of 0.”

3 / 10
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Anonymous · Taken for 5 to 10 years · September 5, 2014

“I started Eligard in 2006 and it worked well until 2012. I started taking Casodex with the Eligard injections and that worked well until early 2014. I came off the Casodex at that time and continued to take the Eligard with my PSA back up to 7.1 and cancer mets to my T3, T4 spine. I had radiation to my spine and now waiting for financial assistance on new medicine.”

9 / 10
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Harvey Dolan · Taken for 6 months to 1 year · November 21, 2021

“I was given despite having informed the Radiation Oncologist that I had absolutely no interest in receiving this castrating hormone. He didn't properly convey my wishes and a VA Urologist ordered it anyway. It's been a complete and utter disaster. I have suffered night sweats, lost muscle mass, increased insomnia, testicular shrinkage, and lost libido. It should be emphasized that I had only intermediate level prostate cancer after 11 years and therefore was not an appropriate candidate for this "chemical garbage".”

1 / 10
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Patient 007 #2 · Taken for 1 to 2 years · February 7, 2022

“Hello. This is an update...I posted last year (2021). I have now had 5 shots of 3 months Eligard. I only have 3 left to complete the 2 year treatment. I had (have) Stage 3 prostate cancer, it spread to the lymph nodes, but no further (they think!). No surgery since it spread...I had my last (45th) Radiation treatment 6/9/21. Back to the Eligard. I was about to stop (after 3) or slow down the injections due to the crappy side effects, but Oncologist talked me into continuing. I am counting the months until I am done. My biggest side effect is bad headaches for several weeks after each injection. Yes, I get the hot flashes, I'm dizzy...sleep sucks, joint pain....and now my knees are very painful. My PSA did drop from mid 20's to .06 (almost nothing). That's the good part, I guess. I'm just hoping I can tolerate it all. GOOD LUCK!”

4 / 10
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Mike · Taken for 6 months to 1 year · September 23, 2021

“I, like others have posted, feel I've had enough. 7 months of 'monthly' injections, not too many bad side effects until month 7 now I just felt it overloaded my body. I stopped for 2 months and just had a 3 month injection, being told it would not be as invasive, rubbish as I am now back in the throes of strange side effects, mostly constant diarrhea, bowel incontinence, all 24/7 hot flashes. The same reason I stopped Casodex after 3 months due to severe "hand and foot syndrome". I can control the mental aspects, but I think but this was my last injection. Sure, the traditional approach probably saved my life but every body is different in terms of the post radiation treatments. Obviously check with your Doctor before a decision like this!!! ...But "Traditional" has to be modified depending on the individual.”

3 / 10
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Johnny · Taken for 2 to 5 years · March 30, 2022

“If you are interested, watch a YT video called, “High PSA (prostate specific antigen) is NOT a diagnosis for prostate cancer.” I watched this after having elegard treatments. The video made me angry but it was eye opening. Was diagnosed with Prostate cancer in 2014. I was treated with radioactive seeds, it worked for just over 1 1/2 years! My PSA started climbing so I was given Lupron injections. The Lupron injections kept my PSA down just over 1 1/2 years. After a period of time without any injections, my PSA started rising again so my DR started me on Lupron injections, the Lupron injections brought my PSA back down again. Then the side effects started, I never thought a person could go through so much misery! The only way I could handle it was giving all what I was going through to Jesus Christ! Loss of muscle mass plus. Now after receiving these Eligard injections my PSA is starting to rise again?? I’ve lost so much muscle mass, I stopped Eligard!”

4 / 10
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