Contraindications: Do not use Norditropin 45 IU in individuals with active malignancy, diabetic retinopathy, closed epiphyseal plates in growing adolescents, or known hypersensitivity to somatropin or any vial excipient. Individuals with acute critical illness, respiratory failure, or complications following open-heart surgery should not initiate somatropin therapy.
Side Effects: Reported adverse effects include peripheral fluid accumulation in extremities, joint discomfort during dose escalation, transient glucose tolerance changes, and injection-site reactions (redness, induration). Paraesthesia of the hands may appear at higher doses and typically resolves with dose adjustment rather than full discontinuation.
Monitoring: Monitor fasting plasma glucose and HbA1c at baseline and every 6–8 weeks during active use, as somatropin exerts counter-regulatory effects on insulin sensitivity. Palpate injection sites weekly for signs of lipohypertrophy. Inspect each reconstituted vial before every injection — discard immediately if appearance deviates from clear and colourless.
PCT: Exogenous somatropin does not suppress endogenous testosterone production or the hypothalamic-pituitary-gonadal axis, so conventional PCT agents are not required specifically for HGH cessation. However, if somatropin has been stacked with anabolic-androgenic compounds, the PCT protocol for those agents should proceed per standard guidance, independent of HGH taper.