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User Reviews for Tasigna to treat Chronic Myelogenous Leukemia

Tasigna has an average rating of 7.8 out of 10 from a total of 24 ratings for the treatment of Chronic Myelogenous Leukemia. 71% of those users who reviewed Tasigna reported a positive effect, while 13% reported a negative effect.

Tasigna Rating Summary

7.8/10 Average Rating

24 ratings from 27 user reviews

Compare all 23 medications used in the treatment of Chronic Myelogenous Leukemia.

46% 11
17% 4
8% 2
0% 0
13% 3
0% 0
4% 1
0% 0
0% 0
13% 3

Reviews for Tasigna

Mountainman555 · Taken for 1 to 2 years January 25, 2021

“Tasigna has been a very effective medication for my CML. (chronic myeloid leukemia). My BCR/ABL counts have quickly dropped and are now hovering from .3 to .06 parts per X. Fortunately for me, any side effects from the medication are not felt. I have been taking two 150mg tablets twice daily since October 2019. I sort of wish some researcher would ask me about my life history or something to see what may of caused this kind of Leukemia. Apparently the only indications are being exposed to nuclear fall-out. I was not in Nagasake or Hiroshima. But I have visited Utah's west desert, Skull Valley a couple of times.”

10 / 10
BD · Taken for 5 to 10 years January 23, 2021

“Easy to use. I take one capsule twice a day. I have no side effects from the drug. I’m fortunate to have VA benefits to pay for it as the actual cost would make it prohibitively expensive for most.”

10 / 10
JWald · Taken for 5 to 10 years July 25, 2020

“I was on Tasigna since first approval (2007) due to side effects of Gleevec. I had good CML results with little seen side effects. In 2017, I started having atherosclerosis, leading to heart attack and 4 stents. They said was directly related to the medication due to never smoking, my cholesterol was good, there were no other pre-cursers for this. After which I had 2 strokes which the team of doctors believe was a wash out of this same condition. I now have to get a pacemaker. Not sure if this has anything to do with all of the above But would never wish this on anyone.”

1 / 10
Sam · Taken for 2 to 5 years April 15, 2020

“Started Tasigna a little over 4 years ago. Have taken 200mg dose twice a day ever since. Brought me from 56% cancerous white blood cells to 2% in just a few months, molecular remission within about 1 year and has kept me there . Still suffer from insomnia, bone and muscle pain, but rashes went away after a couple years. Neuropathy in feet and toes but I worry that peripheral artery disease is occurring also... Even with breaks (1-2 weeks) I never feel any better so the breaks are hardly worth taking. Novartis patient assistance program took care of me for the first year and the Medicaid ever since with nothing out of pocket thank God. TASIGNA HAS KEPT ME ALIVE...”

9 / 10
mdr007 · Taken for 10 years or more March 18, 2020

“Been taking Tasigna over 11 years now. Been in complete remission for almost the entire time. Worked quickly and amazingly well. No side effects to speak of. Tried going off it once but CML returned. Went back on Tasigna and quickly was back I complete remission. A wonder drug to be sure. Started at age 41 and take one 200 mg capsule daily. I am lucky and grateful. Best of luck to all those with CML!”

10 / 10
CML Dude · Taken for 1 to 6 months February 19, 2020

“Diagnosed with CML and a white count of over 750K (yes you read that right). After 2 months white count fell to 5K (middle of normal range). The two "fasting windows" per day that are required are a hassle but you get used to it. Light to moderate bone pain occasionally but most days there is none. Slightly dry skin on and off but not too bad. Insurance covers (UHC) with a STEEP co-pay (arond $1300 per month!) but that makes me hit max out of pocket (MOOP) by March of every year so in that respect no more expensive than anything else since I'd hit MOOP anyway.”

9 / 10
Bob · Taken for 1 to 2 years November 9, 2019

“After a year on sprycel it wasn't working so they switched me over to tasigna, it brought my bcr/abl levels down more in 3 months than the whole year on the sprycel, however the 800 mg/day was too much for me and I was neutropenic for several months and needed neupogen injections which was not fun, I've been able to tolerate the 600 mg dosage without any major issues beyond the standard fatigue and bone pain, unfortunately I've yet to reach a major molecular response but hopefully that will happen in the next few months.”

8 / 10
Dgreen71 · Taken for 2 to 5 years November 14, 2018

“I take 2 (150mg) in the morning and 2 at night 12 hours apart. So far my side effects have been minimal. I feel bloated sometimes, but the fatigue seems to never go away. The hardest part of taking this medication is the timeframe with taking meds and eating. In the morning it's not to bad, but in the afternoon, it's difficult, because my kids and wife are all hungry and I have to wait to eat for an hour after I take my meds. Most of the time I just reheat and the eat earlier. The most important thing though is the medication is working and my cancer is barely noticeable besides the side effects.”

8 / 10
Jj philippines February 12, 2017

“Took tasigna 2 tabs in the morning and 2 tabs in the evening. Shes having too many little poop, that made her sleepless. She feels bloated most of the time. She barely sleep .was diagnosed w cml last Jan 2017. Before that it is important. To recognize such symptoms , she is 68 years old, in good healthy eating lifestyle, taking high blood medicines since late her 40's. Does her annual check up at age 55 up to present religiously. No history of family CML except for hepatitis b her sister. She started having WBC high of feb.2016 from normal 10,000 went to 35,000. Doctors thought its just an infection took 1-3 antibiotics between , starting august with onset fatigue, hard breathing and hypoglycemia, which she never had sugar problem before”

IanBench · Taken for less than 1 month November 30, 2016

“Started Tasigna on Thursday morning. I'm diabetic and became severely hypoglycemic on Saturday. Stopped taking diabetes meds, and that improved, but I had a stomach ache and nausea so bad I was dry heaving for 3 solid days, because I couldn't eat. Went 3 days without sleep because I was curled up around the toilet. I stopped taking it on Monday evening. My reaction to this drug felt like what I invision chemo to be. I go back to my doctor tomorrow to come up with an alternative treatment plan. I'm now scared to start another med, for fear of similar reactions, and I don't want to imagine this sick the rest of my life. Very happy and envious of all the success stories.”

1 / 10
JaynaQT February 15, 2016

“After Gleevec quit working after five years, and no remission, Tasigna has been a wonderful medicine. Thinning hair, a little hip pain and some blisters/itching...but so much blessing to have achieved molecular remission in 4 mos. and continued for 3 yrs. now. Doc has reduced my dose from 600 to 400mgs to see if rashes stop and pain subsides. hopefully, won't have to go back up. The cost is insanity...good thing I get assistance or I wouldn't be here. ”

10 / 10
Miss Jacqueline · Taken for 2 to 5 years September 1, 2015

“I have been on Tasigna for just over 3 years now (300mg x 2 times a day) Tasigna worked for me within a few weeks I have been in remission for basically the entire 3 years. As for the side effects, I feel sick to my stomach, tired, severe leg and arm pain, I can't walk to long without needing a break, I went from working full time to not working at all because I am so tired all the time.... but hey I am in remission and alive so is all the above really a problem? Nope”

10 / 10
Wolfs Blood · Taken for 5 to 10 years August 8, 2014

“Started on Gleevec in 2005, I was having hard time with side effects. Sometime early 2007 I heard they were working with Tasigna, It was under a number at that point. I asked my Doctor if I could get on the study. After some testing and paperwork, I finally got on it. Great, I had been told prior that I would never reach molecular remission. After several months on Tasigna, I received a phone call at my house late one evening. My Doctor was surprised, and happy to tell me, there were no signs of my leukemia and I was in a molecular remission. At That time they still had me on 800 mg a day. I had the typical side effects with light rash, some hair loss and some bone pain. Several years later I was reduced to 600 mg and am on that now.”

10 / 10
jj mn · Taken for 1 to 6 months June 18, 2014

“Brought my BCR ABL levels down where Gleevec and Sprycel didn't, at least for my specific situation. I had to waste 9 months of treatment to find out Tasigna was the right medicine for me. Lucky I worked so hard to fight for it that is what it takes. Works great for ph refractory on other medicines before transplant.”

10 / 10
Alexis7092 November 21, 2013

“I was diagnosed in 2009 and started taking it while it was just a study pill. I did get joint pain pretty bad. I was in remission about a year later. The joint pain was bothersome and I had to take it for life. Well I stopped taking it in 02/2012. I told myself I was a lot better. Well guess what my leukemia is back. I need to go see my doctor again and need to get back on it. So everyone please don't stop taking it like I did. I hope and Pray that I will fight it again and win again.”

10 / 10
kenison July 30, 2013

“Had a reaction ended up in hospital. Can't take it.”

juditweety · Taken for 2 to 5 years April 21, 2013

“I was diagnosed with Chronic Myelogenous Leukemia in October of 2010. I was prescribed 600 units of Tasinga per day - 300 AM, AND 300 PM. I was in remission in 12 days - thank GOD. I am on Medicare and get help with my co-pay from PSI. I have mild nausea when I first take the pills, mild constipation and some shortness of breath, but I also have COPD. I have, been taking Tasinga for 2 1/2 yrs now and am just starting to notice my hair is thinning. I was told I have to take it for life. I thank GOD everyday for this medicine and will gladly endur the minor side efforts in exchange for a longer life. ”

10 / 10
sandyakk · Taken for 1 to 6 months March 30, 2013

“I have had a very positive experience with Tasigna. Very little side effects compared to the Gleevec. My body seems to tolerate it much better than the Gleevec.”

10 / 10
Flycatcher · Taken for 1 to 6 months March 30, 2013

“I have been on Tasigna since being diagnosed in November 2013. Given how I felt at the point of diagnosis, I am so happy with Tasigna. I have minor side effects and my energy level has been great. Early results are great. Time will tell.”

9 / 10
Anonymous · Taken for 2 to 5 years July 25, 2012

“Some joint pain at the beginning and constipation at first, but no problems afterwards”

10 / 10
sophieleo May 24, 2012

“After 18 months of taking Gleevec without having the best results, taking Tasigna was a gift as the side effects cannot be compared with those of Gleevec. Although after taking it for more than a year, my BCR ABL exams are going up and down and I suppose Ii have to change my meditation again.”

Anonymous August 3, 2011

“I started using Tasigna after an year of non working Gleevec. It has brought me to remission state. I am and my doctor are very happy. Yes rose comes with thorns. It has affected my hearing and I have redness and crusting around my head which turn into painful pimples. But still it is great drug which has brought me the cure.”

4 / 10
Magicmack July 28, 2011

“The timing for eating is a pain. I have become hyperthyroid as a result of this medicine, and my hands started shaking, and I lost 40 pounds. I had been hypothyroid before! I like the weight loss, but the hyperthyroidism has caused digestive problems, and my eyes bulge a bit. Have suffered drug interactions with Cipro (heart) and maybe Lexapro (acute Achilles tendonitis). Unfortunately,my Dr was not familiar with what Tasigna could do----”

6 / 10
Anonymous May 13, 2011

“2 years on Gleevec with minimal positive effect and maximum side effects. 3 months on Tasigna and swelling-gone, leg pain-gone, nausea-gone, I feel good. Tests show much improvement and my Doctor is now very optimistic. Twice a day regime and eating times are small problems. My libido is back.”

9 / 10
McLay March 25, 2010

“Effective drug, 12 hour thing is a pain as is the eating discipline. Must affect hemoglobin levels as feeling tired is an issue. Any effort i.e., walking up a slight incline can make you feel nauseous. Can't complain because it works for me.”

6 / 10

This information is NOT intended to endorse any particular medication. While these reviews might be helpful, they are not a substitute for the expertise, knowledge and judgement of healthcare practitioners.

Learn more about Chronic Myelogenous Leukemia

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