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Testosterone Cypionate 200mg 10ml – Watson Steroid in USA



Each vial contains:

Testosterone Cypionate 200 mg.


The main natural androgen Testosterone is responsible for the development and maintenance of male secondary sexual characteristics, exerting important anabolic action. This last property contributes, above all, to the acceleration of the growth process at puberty by stimulating bone growth and modulating the welding process of the epiphysis of long bones.

In the form of Cypionate, it has a prolonged therapeutic action, once it has been hydrolyzed in vivo to free Testosterone, being superior to Propionate in this aspect. Testosterone Cypionate is approximately 99% strongly bound to plasma proteins and 80% to globulin, 19% to albumin, and 1% free). It is biotransformed in the liver and eliminated mainly in the urine. Its half life as intramuscular Cypionate is approximately 8 days. In white tissues it is converted to 5-alpha-dihydrotestosterone, which suppresses GHR, LH and FSH by negative feedback.

Testosterone Cypionate 200mg 10ml – Watson Steroid in USA


In a normal man, Testosterone stimulates erythrocyte production because it favors the synthesis of erythropoiesis-stimulating factors.

Therapeutic indications:

Congenital or acquired primary hypogonadism, when there is testicular insufficiency due to cryptorchidism, bilateral torsion, testicular absence syndrome or orchidectomy. Hypogonadrotrophic hypogonadism: when there is congenital or acquired deficiency of LH-RH (luteinizing hormone-releasing hormone) or hypothalamic-pituitary damage due to surgeries, traumas, tumors or radiation.

Delayed puberty, when there is a family pattern of delayed puberty, not secondary to a pathological disorder, in patients who did not respond to psychological support therapy.

Male climacteric: as a substitute therapy in impotence or other symptoms associated with this disorder, when the etiology is due to a confirmed androgen deficiency. Severe malnutrition, myelofibrous aplastic anemia, myelosclerosis, agnogenic myeloid metaplasia, hypoplastic anemias caused by malignancy or myelotoxic drugs. Inoperable carcinoma of the breast in women with tumors that are hormone responsive or have previously demonstrated a response to hormone therapy.

Adverse reactions:

The following reactions require medical monitoring:

Virilization and menstrual irregularities in women, irritability of the bladder, gynecomastia, anaphylaxis, edema, erythrocytosis, gastrointestinal irritation, hypercalcemia and polycythemia, androgenic alopecia, seborrhea and acne in men and women.

Carcinoma prostatic hypertrophy and an increased sexual desire develops in patients. These are adverse reactions of rare incidence during long term therapy or with high doses. Hepatic necrosis, leukopenia, hepatic purpura.

Other adverse reactions are: constipation, nausea, diarrhea, infection, redness, pain or irritation at the injection site, libido changes, stomach pain, difficulty sleeping, impotence, testicular atrophy, headache, anxiety, depression, paraesthesia generalized, sleep apnea, skin rash.


It is contraindicated in patients with breast cancer (male), diagnosed or suspected prostate cancer or adenoma, severe heart, liver or kidney failure in prepubertal or aggressive individuals, pregnancy.


Hypogonadism, climacteric and impotence (male replacement therapy): 60-400 mg. I.M. every 2 to 4 weeks.

Male delayed puberty (replacement therapy): 25 to 200 mg. Every 2 to 4 weeks, for a period usually limited to 6 months.

Antineoplastic, in inoperable breast cancer (female): 200 to 400 mg. I.M. every 2 to 4 weeks.

Cautions and warnings:

In the palliative treatment of breast cancer, do not continue therapy if after 3 months the disease continues again or if hypocalcemia was verified in any phase of it. Androgen therapy in women, even for a certain duration, can produce virilization, particularly vocal and hairy.

In children, this drug should be used with caution due to adverse effects on the process of bone maturation, which may be accelerated without producing compensatory gains in linear growth.

When male patients over 50 years of age are treated with androgens, the risk of prostate enlargement or the development of prostate cancer becomes greater. For this reason, prostate and blood tests are frequently performed before prescribing androgens for men of this age.

Oligospermia, azoospermia or reduced sperm function may occur during long-term treatment, resulting in possible infertility, with spontaneous remission after discontinuation of treatment. Patients with acute prostatic hypertrophy may develop acute urethral obstruction, requiring immediate discontinuation of medication.

Urinary serum calcium levels should be determined frequently in women with metastatic breast carcinoma under treatment with testosterone. During treatment with prepubertal minors, bone X-rays should be taken every 6 months. In patients with acute intermittent porphyria, androgens can precipitate attacks of this condition.

It is usually preferable to start treatment with full doses and adjust later to individual characteristics.

Drug interaction:

Testoland – Depot can react with the following drugs:

Adenoglyco or mineralocorticoids: Corticotropin, foods or medicines that contain sodium (they can increase the risk of edema, predispose acne).

Oral antidiabetics or insulin because there may be a reduction in serum glucose levels.


Hepatotoxic drugs (hepatotoxicity is increased).


Frequent doses can trigger symptoms of slow remission, as it is a long acting drug. Immediate discontinuation of the medication is recommended.


The use of a wet needle or syringe can cause cloudiness of the solution that does not affect the effectiveness of the long-acting drug. If crystals form in the ampoules, heating or shaking may dissolve the crystals. The intramuscular injection should be administered deep into the gluteal or deltoid muscle. Do not administer intravenously. Store at 15° – 30° C and protect from freezing.

Shake before using.

Buy Testosterone Cypionate online USA.


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