contraindications: Contraindicated in individuals with confirmed androgen-sensitive prostate or breast carcinoma.
Not for use by women of childbearing potential or during pregnancy; virilisation risk is present even at conservative doses.
Contraindicated in patients with active hepatic impairment, polycythaemia, or untreated hypercalcaemia.
Do not use if hypersensitivity to Methenolone, sesame oil, benzyl alcohol, or benzyl benzoate has been established.
side_effects: Androgenic: accelerated scalp hair thinning in genetically predisposed individuals; mild acne at injection sites possible.
Cardiovascular: suppression of HDL cholesterol — exacerbated in multi-compound stacks; LDL elevation possible.
Endocrine: hypothalamic-pituitary-gonadal axis suppression proportional to dose and cycle duration.
Haematological: erythrocytosis (elevated haematocrit) especially when co-administered with testosterone.
monitoring: Full blood count and haematocrit every 6 weeks when stacking with erythropoietic androgens.
Lipid panel (HDL, LDL, triglycerides) at cycle start and mid-cycle to track cardiovascular risk in multi-compound protocols.
Liver enzyme panel (ALT, AST) if oral compounds are used concurrently in the stack.
Blood pressure measured weekly during any stack; hypertension warrants immediate dose reduction of the most androgenic co-compound.
pct: Begin PCT after the washout period of the longest-estered compound in the stack, not Methenolone Enanthate alone.
SERM-based PCT (clomiphene citrate 50 mg/day or tamoxifen 20 mg/day for 4–6 weeks) is the standard recovery framework.
Baseline testosterone and LH/FSH blood work should be obtained before PCT initiation to establish the degree of suppression.
PCT duration may need extension to 8 weeks following lengthy multi-compound cycles of 16+ weeks.