Has anyone had a crazy extreme increase for their pulmozyme?
Ours went from 60 dollars a month to 1,297.28 a month!
Thank goodness we have a secondary insurance for my son that pays our copays, but we might not for our daughter once she is born.
I talked the local CF clinic and was told about programs out there to help with co-pays but wanted to know if anyone else had an increase?
Something even crazier is that the drug is over $5000 dollars from the pharmacy we are forced to use (by our health insurance company), but when someone from the CF team contacted a rep from the company that makes pulmozyme they were told that the drug costs around $2500
Maybe there is a reason why the pharmacys contracted rate is so high but I can't figure it out.
Ours went from 60 dollars a month to 1,297.28 a month!
Thank goodness we have a secondary insurance for my son that pays our copays, but we might not for our daughter once she is born.
I talked the local CF clinic and was told about programs out there to help with co-pays but wanted to know if anyone else had an increase?
Something even crazier is that the drug is over $5000 dollars from the pharmacy we are forced to use (by our health insurance company), but when someone from the CF team contacted a rep from the company that makes pulmozyme they were told that the drug costs around $2500
Maybe there is a reason why the pharmacys contracted rate is so high but I can't figure it out.