“…T 1 liver enhancement after intravenous infusion begins early, 1−2 min postinjection, maximizes within 5−10 min, and persists for several hours, allowing flexibility for patient scheduling when compared to Gd 3+ chelates. No longer on the market, for human clinical imaging to detect hepatic lesions, the approved dosage of Mn-DPDP was 5 μmol/kg, and approximately 15% was eliminated in the urine by 24 h postinjection and 59% in the feces by 5 days . In a European phase III clinical trial, adverse events, such as nausea, headache, and pruritus, were observed in 7% of the 624 patients. , Transient decreases in alkaline phosphatase levels and sensations of heat and flushing with high injection rates most likely related to peripheral vasodilatation have also been reported.…”