Darzalex and myeloma | MyMyelomaTeam

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Top 10 Search Results for "Darzalex"

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Darzalex
A MyMyelomaTeam Member asked a question 💭

I am on Velcade ,Daralex,and Des,every week for at least 1 year,had a bad reaction the first week,they gave me 100 m of fast acting steroids in my veinsit helped the chills and blood pressure immediately,but the pain was severe for 2 hours,my second week had r
delayed reaction the next day took benadryl steroids,got because in 1 hour,3 treatment was yesterday and no reaction

A MyMyelomaTeam Member

There is a subcutaneous (below the skin) injection form of Darzalex available. I started with intravenous but my veins did not hold up. So the injection works great and only at the cancer center once… read more

IGG Lambda Patients Taking Pomalyst
A MyMyelomaTeam Member asked a question 💭

Hi I was wondering how many milligrams are you taking of Pomalyst and how long did it take to reach a complete response? So far it’s working but very slowly.

A MyMyelomaTeam Member

Oh Laurie I hope the change in the Pomalyst works for you. Keep us posted on how you’re doing.

I’m Getting Neuropathy From Velcade, I’m Being Changed To Darzalex . Anyone With Feedback On Side Effects? Thanks
A MyMyelomaTeam Member asked a question 💭
A MyMyelomaTeam Member

I got Neuropathy from Velcade in 2012, I started talking vitamin B-12 and it is helping me better than Gabapentin.

Darzolax
A MyMyelomaTeam Member asked a question 💭

Has anyone declined to add darzolax to the therapy they are already On? I received my clonol seq results. 2 cells per million. Hope everyone is well. Have an active weekend.

A MyMyelomaTeam Member

Update on darzolax, Saw my Dr. Yesterday, he and his colleagues have agreed with me to not pursue the darzolax therapy at this time. They do want me to up my revlimid from 10g to 15g. Which I'm ok… read more

Nerve Or Back Pain From Darzalex ?
A MyMyelomaTeam Member asked a question 💭

Has anyone developed back pain from taking Daralex? Joint, back and nerve pain are listed as common side effects. I have developed nerve pain going into my right shoulder. Not sure if this is related to the Daralex or swimming. Doctor says it is not Myeloma related.

A MyMyelomaTeam Member

I have been on this drug since mm started to attack me for a 2nd time. I am tired but only have to take it once a month now. Attitude is everything. Never believe anything is stronger than… read more

BETA 2 Microglobulin Serum High
A MyMyelomaTeam Member asked a question 💭

Just received my blood results back, B2M JUNE 1 2021 4.97H MAY 4.62.H APR 3.09 H
Pretty worried since I read way to much today. My Protein went down to 7.3 from 10.4 so that was good.
Going to call doctor tomorrow. Any ideas what is going on. I am on Velcade, Darzalex and steroids. 9 treatments but now every three weeks thinking I was doing good maybe I have to go back to weekly.

A MyMyelomaTeam Member

Our oncologist said not to worry about slight variances in test numbers. The ones to worry about are the drastic changes from one blood test to another. Usual procedure is to wait and do the same… read more

Darzalex
A MyMyelomaTeam Member asked a question 💭

I am a bit worried...I get Vertigo really bad..so I hope that the Darzalex will be o.k. I am being put on Darzalex Fast Pro

A MyMyelomaTeam Member

I have tinnitus too. It can be very annoying. Mine started with my myeloma diagnosis. Weird.

Daratumumab+Dexamethasone For Smoldering Myloma And Al Amyloidosis
A MyMyelomaTeam Member asked a question 💭

I am taking Daratumumab+Dexamethasone for SMM and AL Amyloidosis. Has anyone else taken Daratumumab+ Dexamethasone alone for SMM or AL Amyloidosis or both? Or does anyone take Daratumumab + another single drug for them? If so what? If you take a triplet also let me know what please.

A MyMyelomaTeam Member

I take Dara, revlimed, and dexamethasone for smm

Anyone Have Experience With Darzalex? My Wife Is Starting Next Week
A MyMyelomaTeam Member asked a question 💭
A MyMyelomaTeam Member

My doctor attaches a smaller needle and they kind of continuously lightly pinch the area around the shot. I didn’t have a mark/bruise last week!

Runny Nose Whenever I Eat .
A MyMyelomaTeam Member asked a question 💭

Here’s a good question for everyone. Ever since I was diagnosed with MM whenever I eat food, whether it’s hot or cold, my nose runs. My Oncologist has no explanation for this happening. I went to an ear, nose and throat specialist and as soon as I said Cancer he dismissed me. Any body with the same experience? It’s a little embarrassing when I go to a restaurant.

A MyMyelomaTeam Member

My nose runs all the time, especially when I eat. I blame it on the Darzalex.