dangerous

BANNED

Do Not Use

Nandrolone (Deca-Durabolin)

Prohibited by DEA, WADA, FDA (without Rx)

warningIllegal possession is a felony. Most supply is from black market/counterfeits.

Nandrolone (Deca-Durabolin)

PROHORMONE

Also known as: Deca, NPP, Nandrolone Phenylpropionate, 19-nortestosterone

What is Nandrolone (Deca-Durabolin)?

Nandrolone is an anabolic androgenic steroid classified as a Schedule III controlled substance. Illegal possession is a felony. Most gym supply is from black market with unknown purity.

Why is Nandrolone (Deca-Durabolin) Banned?

Controlled substance with abuse potential and significant health risks. Illegal without prescription. Black market products often contaminated.

Banned by DEABanned by WADABanned by FDA (without Rx)

Health Risks & Side Effects

warningCommon Side Effects

  • arrow_rightLiver toxicity
  • arrow_rightCardiovascular effects
  • arrow_rightTesticular atrophy
  • arrow_rightGynecomastia
  • arrow_rightVirilization in women
  • arrow_rightMood effects

blockContraindications

  • arrow_rightProstate cancer
  • arrow_rightBreast cancer
  • arrow_rightHeart disease
  • arrow_rightLiver disease
  • arrow_rightPregnancy

How Does Nandrolone (Deca-Durabolin) Work?

Synthetic androgen. Binds to androgen receptors, stimulating protein synthesis and muscle growth. Suppresses natural testosterone production.

History

Developed in the 1950s for medical use. Classified as Schedule III controlled substance under the Anabolic Steroid Control Act. Still prescribed rarely for anemia and wasting diseases.

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Learn More

Research articles and educational resources

science

Scientific Research

From PubMed • 3 peer-reviewed studies

Safety and efficacy of nandrolone decanoate for treatment of wasting in patients with HIV infection.

AIDS (London, England)1997Gold J, High H A et al.

To evaluate the safety and efficacy of the anabolic steroid, nandrolone decanoate (Deca Durabolin) in patients with HIV wasting who are resistant to nutritional intervention.

Effects of nandrolone decanoate on the neuromuscular junction of rats submitted to swimming.

Comparative biochemistry and physiology. Toxicology & pharmacology : CBP2006Cavalcante W L G, Dal Pai-Silva M et al.

This study addressed the effects of nandrolone decanoate (ND) on contractile properties and muscle fiber characteristics of rats submitted to swimming. Male Wistar rats were grouped in sedentary (S), swimming (Sw), sedentary+ND (SND), and swimming+ND (SwND), six animals per group. ND (3 mg/kg) was injected (subcutaneously) 5 days/week, for 4 weeks. Swimming consisted of 60-min sessions (load 2%), 5 days/week, for 4 weeks. After this period, the sciatic nerve extensor digitorum longus (EDL) muscle was isolated for myographic recordings. Fatigue resistance was assessed by the percent (%) decline of 180 direct tetanic contractions (30 Hz). Safety margin of synaptic transmission was determined from the resistance to the blockade of indirectly evoked twitches (0.5 Hz) induced by pancuronium (5 to 9x10(-7) M). EDL muscles were also submitted to histological and histochemical analysis (haematoxylin-eosin (HE); nicotinamide adenine dinucleotide-tetrazolium reductase (NADH-TR)). Significant differences were detected by two-way ANOVA (p<0.05). ND did not change body mass, fatigue resistance or kinetic properties of indirect twitches in either sedentary or swimming rats. In contrast, ND reduced the safety margin of synaptic transmission in sedentary animals (SND=53.3+/-4.7% vs. S=75.7+/-2.0%), but did not affect the safety margin in the swimming rats (SwND=75.81+/-3.1% vs. Sw=71.0+/-4.0%). No significant difference in fiber type proportions or diameters was observed in EDL muscle of any experimental group. These results indicate that ND does not act as an ergogenic reinforcement in rats submitted to 4 weeks of swimming. On the other hand, this study revealed an important toxic effect of ND, that it reduces the safety margin of synaptic transmission in sedentary animals. Such an effect is masked when associated with physical exercise.

Nandrolone decanoate for men with osteoporosis.

American journal of therapeutics2000Hamdy R C, Moore S W et al.

To compare the efficacy and safety of nandrolone decanoate and calcium (NDC) with those of calcium alone (CAL) in men with idiopathic osteoporosis, a 12-month, randomized, prospective, controlled study, was performed in an outpatient clinic. Twenty-one men with idiopathic osteoporosis (as determined by radiological and dual energy x-ray absorptiometry findings) were randomly allocated to either 50 mg nandrolone decanoate intramuscularly (im) weekly and 1,000 mg oral calcium carbonate daily (NDC group) or to 1,000 mg oral calcium carbonate daily (CAL group). Bone densitometry (total body, left femur, and lumbar spine), serum, and urine biochemical parameters were measured at 3-month intervals. In the NDC group, bone mineral density initially increased, reached a plateau, and then decreased to near baseline levels at 12 months. Increases in lean muscle mass mirrored these changes. Free and total testosterone significantly decreased. Hemoglobin increased in all patients in this group. Patients in the CAL group exhibited no significant change in either total body or bone mineral density or biochemical parameters. Thus, nandrolone decanoate, 50 mg im weekly, transiently increases the bone mass of men with idiopathic osteoporosis in this preliminary study. Careful monitoring is necessary.

Data sourced from Wikipedia and PubMed