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Why it was included in the FDA ban The FDA cites significant safety risks due to the potential for congestive heart failure in certain patients seen in a clinical trial that was terminated

Signs of improper reconstitution can include visible particles in the solution, cloudiness, or a failure of the peptide to fully dissolve

Pancreatitis: Severe, persistent upper abdominal pain particularly pain radiating to the back may indicate acute pancreatitis, a serious adverse event associated with the incretin drug class

Locomotor pattern in paraplegic patients: training effects and recovery of spinal cord function

Secondary recanalization after lysis of the clots which cause obstruction early in the reaction, and the subsequent bleeding after several weeks, could explain why foam-sclerosed veins fill up again with blood around the 6th week