Boehringer Ingelheim, in collaboration with Zealand Pharma, will likely be the next big challenger after advancing its promising candidate survodutide, a GCGR/GLP-1R dual agonist, to Phase 3 clinical trials last year
Bring the laboratory requisition and required identification
While the FDA approved doses of 0.5 mg and 1.0 mg for diabetes management, the agency has also issued warnings about potential risks including pancreatitis, thyroid cancer concerns based on animal studies, and other serious adverse events
Dakin CL, Gunn I, Small CJ, et al
If this is the case, you still have options: Check if you qualify for partial reimbursement for dietitian visits outside the network, use your HSA or FSA account, see if your employer wellness program includes nutrition counseling, or get in touch with our team to learn more about alternative payment plans for self-paying clients
It is not an over-the-counter substitute for diabetes medication