I have been taking Niraparib for nine weeks now .At my oncologist appt in January I asked to have my BP checked as the “ book” I was given when I started on the tablets says it should be done monthly .After much rolling of eyes and “ we have loads of women on that drug , we don’t usually check BP “ they finally checked and it was high .Referred to GP to sort it out .Now I am taking BP tablets to help bring it down .Has anyone else had high BP as a side effect and if so and you are no longer taking Niraparib did they let you come off the BP meds ? .Thanks and love to everyone on this grey ( London) Thursday morning xxx Julia
Niraparib side effects: I have been taking... - My Ovacome
Niraparib side effects
Hi Juleswhee I am not on this drug but have experienced this attitude to bp checks- I bought a machine and now do it myself xx
Hi Jules. Can't share Niraparib experiences but am dealing with recent high blood pressure myself, which my oncologist attributes to Avastin.
So far, it's kept mostly under control by a run off the mill hypertension medicine... Ramipril.
I think it's a good idea indeed to have your own bp meter and measure on a regular basis. What a bother you had there ...
Hope you get it under control soon. Xx. Maus
I’m really surprised at their response . It is a common side- effect . Mine is done monthly at Clinic . ( been on it almost 5 months now ) . Initially at the Clinic it was very high but they’ thought it was ‘ white coat syndrome ‘ & asked me to keep a record & monitor at home . I took it twice daily , then daily & now every few days & it’s reasonable. So haven’t needed pills yet . I think It’s a good idea to get your own machine & it’s more relaxing at home . Hope that helps & wishing you all the best .
Mary x
Hi Mary , For some things my cancer centre is brilliant but others not so , it’s a good job I am on the ball and read all the notes . I had to have a 24 hr monitor attached which is supposed to show true readings and not invoke “ white coat syndrome” however for some reason I found it very stressful , well having the life squeezed out of your arm every half hour can do that to you .Hopefully the BP tablets will stabilise it .Thanks for answering xx Julia xx
Yes I would find that stressful too . I try & do deep breathing & think of a lovely beach before I take mine . But the second I have a worrying thought , it shoots up !
X
With apologies this is bad medical or nursing practice. They can miss so much by not doing BP and weight measurements every visit. The first Oncologist I saw measured weight and BP at the first visit and only after a "crash" did it again finding that my weight had reduced significantly enough to lower the dose. Please do yourself a favour and insist they do it each visit especially if a month apart.
I think the oncologists should know the common side effects of the drugs they commonly prescribe. Di
Absolutely , wonder if there are any others on this site taking Niraparib who don’t have their BP taken regularly .xx
Hi, Julia! So sorry you were met with the rolling eyes syndrome. I have been having issues with medical staff (outside of my onc team) with not listening or giving two craps about the fact that OC is my PRIMARY issue.
I started out with a High BP which was only enforced by chemo and then Zejula. (Niraparib). My cardio dr increased my BP med and added a diuretic. Seems to be working.
The only other issue I had on Zejula was the low platelets so I'm on the lowest dose of 100mg. Glad you are with a GP who can assist you with bringing down your BP. The best of luck and love to you!
Marisa
Hi Marisa , Thanks for the reply . My GP was on the ball so just hoping the reading goes down .Having OC is hard enough without having to deal with other health issues.Taking 200mg of zejula , no platelet issues at the moment and ca125 finally coming down .xxxJulia
Hi Juleswhee, are you ok, not seen you on here for a while 💞