anonymous
Guest
anonymous
Guest
Several questions about this impending launch:
What is the hurry to launch?
Why will we be selling a drug from June 10th-June 16th that cannot be sampled or written?
Why would we not wait to launch until after the summer shutdown? Realize, that as nice as a summer shutdown is with no company emails and no company responsibility, the Obesity reps will be fielding calls from confused offices everyday all day.
Why put Wegovy in a single use, single dose pen when you know there are tolerability issues and you know, despite being off-label, thousands of people use "in-between" doses of Saxenda so that they can stay on therapy and lose weight?
Why would we not let the reps at least have some input on the initial targets for this launch? News Flash Novo: Super busy IM and FP doctors that write a lot of GLP-1 for diabetes, in most cases, are not the big Obesity AOM writers!
Most importantly, why did we eliminate every level of management above the DM level that had any familiarity with the uniqueness of the obesity market?
What is the hurry to launch?
Why will we be selling a drug from June 10th-June 16th that cannot be sampled or written?
Why would we not wait to launch until after the summer shutdown? Realize, that as nice as a summer shutdown is with no company emails and no company responsibility, the Obesity reps will be fielding calls from confused offices everyday all day.
Why put Wegovy in a single use, single dose pen when you know there are tolerability issues and you know, despite being off-label, thousands of people use "in-between" doses of Saxenda so that they can stay on therapy and lose weight?
Why would we not let the reps at least have some input on the initial targets for this launch? News Flash Novo: Super busy IM and FP doctors that write a lot of GLP-1 for diabetes, in most cases, are not the big Obesity AOM writers!
Most importantly, why did we eliminate every level of management above the DM level that had any familiarity with the uniqueness of the obesity market?