Semaglutide: May aid in the treatment of type 2 diabetes mellitus, may reduce cardiovascular mortality and CV events in type 2 diabetes mellitus patients who also have established cardiovascular disease
Use aseptic technique, rotate sites to prevent soreness, and use an appropriate needle (e.g

this off-label use is not backed by the same level of controlled human trial evidence as the lipodystrophy indication Known risks and side effects: Injection site reactions, including erythema, pruritus, pain, and bruising at the injection site Arthralgia (joint pain) and peripheral edema (fluid retention), recognized class effects of GH-axis stimulation Increases in blood glucose and reduced insulin sensitivity, with clinical trials showing a higher rate of elevated HbA1c and new-onset hyperglycemia versus placebo Formation of anti-tesamorelin antibodies, reported in a substantial proportion of treated patients, with unclear long-term clinical significance Contraindicated in people with active malignancy, pituitary or hypothalamic disruption, or pregnancy, per FDA labeling Evidence snapshot: The strongest evidence is a set of Phase 3 human randomized controlled trials that supported FDA approval of tesamorelin for reducing visceral abdominal fat in HIV-associated lipodystrophy (approved 2010), plus a separate placebo-controlled human RCT (Baker et al., 2012, Archives of Neurology) showing improved executive function in older adults

At one injection per week, these risks are minimal
Ozempic and other weight-loss drugs seem to work better for some patients than others and a new study suggests that scientists might know one reason why: Specific genetic variants, which affect how the drugs are encoded by the body