Experiences with

Mavyret

I have just started a Mavyret treatment for Hep C. I contracted it during my teenage addiction to heroin.

I'm thinking doing 8 weeks epclusa. then one week mavyret, so 9 weeks total. I know it would be only another 3 weeks for the standard treatment, but I seriously need to be functioning well mentally by the 20th April.

I have been taking Mavyret for 2 weeks and happy to say NO side effects but I do have a question. I've had Hep C since 1985....after tests 3 weeks ago viral load 4 million …. No Cirrhosis (Great news to find out).

I'm just 3 days away from completing Mavyret treatment and whilst I only had mild side effects I'm a bit worried as my last bloods showed virus was still detected. I m reading bout people being undetected after four weeks so I'm scared it's failed.

I also have Hep C and I'm currently in treatment with the drug Mavyret. Wondering if anybody else can tell me more about their experience with this drug. Thank you very much for reading, Biologist

Hello there.i was on mavyret for 8 weeks.the treatment was successful.i was cured!!

Having terrible nausea from mavyret. Has anyone else had this and what can I take for it?

Had my final blood tests last week after taking Mavyret for 12 weeks. Hospital have confirmed Hep C has completely cleared and no further blood tests or medication is required.

I'd do the Mavyret treatment again in a heartbeat, I have NO regrets! Hope you all have as easy of a treatment as I did!

Just really uncertain if I’m hcv free or not

Hi joined after searching to find people who have been prescribed Maviret for hep c, as it was a bolt out the blue for me, so happy to find such positive people and great results. I'm on day 5 of an 8 week course, diagnosed in 2003 with type 3, never had any treatment, then got letter just 3 weeks ago

Hello everyone!I finished my treatment 2 weeks ago and my last labs show the virus is undetected.thats great news because i had alot of anxiety.I thank God for everything!

Good morning, I hope you are all doing well! Finally I’ve got my 3 months post treatment results Maviret type 3a I’ve been waiting every day for the post for a month with no sign. I had to get the results from my GP in the end. But it’s all good I am still in the clear!🎈🎉💃🤸‍♂️I am so happy it’s

Hi,im on week 5 of mavyret,last week I have developed a chronic cough with some shortness of breath and wheezing.the doctor listened to my lungs and said sounded ok.wondering if anyone has experienced this or did I maybe just pick up a bug. Ty

Hello..so today i went to the dr. and my results from last time show the virus is undetected and i completed treatment.the virus was gone quicker than i thought.i had my labs repeated today at 8 weeks and its looking very good.i have to see my dr. in 3 months for a checkup.im so grateful and anyone else

Hello everyone!today is my 7th week and have 1 week left in treatment.i found out that the virus is undetected...i give all the credit to God.the medication is very effective and it surprised me.overall i hardly had any side affects..mostly fatigue,few headaches, nothing major.iam happy to know its going

Hey everyone!i hope everyone is feeling good enjoying there day..i'm in my last week of treatment and am grateful its not detected..now just going to wait for 3 months for another lab.im feeling relieved

Has anyone finished Mavyret treatment?how did it work for you?currently in my 5th week of treatment...

I'm now 6 weeks into treatment and am wanting to share how im doing.so far i can say that this medicine for me has hardly any side effects. I feel tired but not any where as bad as before without medicine. Mentally i'm in a better place. sometime soon i will find out the results of my labs drawn at 4

Has anyone finished Mavyret treatment? How was their experience?i've been on this medicine for 5 weeks. I already feel better..im not as tired as before..