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Jodi Whittle
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    https://reeltalent.gr/employer/sermorelin-vs-ipamorelin-choosing-the-right-peptide-for-your-needs/

Jodi Whittle, 19

Algeria

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Dianabol Turinabol Cycle Plan PDF

Dianabol Turinabol Cycle Plan



The Dianabol and Turinbol cycle is one of the most popular steroid combinations used by bodybuilders to achieve rapid muscle growth and strength gains. This plan outlines a 12‑week protocol that balances the anabolic effects of both compounds while minimizing side‑effects through strategic dosing, timing, and post‑cycle care.



Week 1–2





Dianabol: 10 mg per day (morning).


Turinbol: 15 mg per day (evening).


Rationale: The initial lower dose allows the body to acclimate, reduces estrogenic conversion of Dianabol and helps prevent early liver stress.



Week 3–6



Dianabol: Increase to 20 mg per day.


Turinbol: Maintain 15 mg per day.


Rationale: By week 3 the body’s aromatase activity has adapted, enabling a safe increase in Dianabol without significant estrogen rise.



Week 7–10



Dianabol: Continue at 20 mg per day.


Turinbol: Increase to 30 mg per day.


Rationale: A gradual rise in Turinol allows for progressive anabolic stimulation while monitoring liver enzymes and hormone levels.



Week 11–12 (Tapering)



Turinbol: Reduce to 15 mg per day, then discontinue.


Dianabol: Gradually reduce dosage over two weeks.



Monitoring Schedule


Parameter Frequency


Liver enzymes (AST/ALT/GGT) Weekly


Testosterone levels Every 2 weeks


LH & FSH Every 4 weeks


Complete blood count Bi-weekly


Hormonal profile (DHEA, cortisol) Monthly


Safety Protocols





Immediate discontinuation if AST or ALT > 3x upper limit of normal.


Re-evaluate any patient with symptoms: jaundice, abdominal pain, fatigue.


Post-treatment follow-up at 6 weeks and 12 weeks for liver function normalization.







Summary




No direct evidence supports the claim that these drugs increase testosterone via aromatase inhibition or CYP3A4 interaction; the literature primarily discusses potential decreases in androgenic activity due to metabolic pathways.


Theoretical mechanisms involve enzyme induction/inhibition, but clinical significance remains uncertain and potentially harmful (e.g., hepatotoxicity).


Recommendation: Use these drugs with caution in patients concerned about testosterone levels or liver function; monitor hepatic enzymes and consider alternative treatments.

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