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Todo Sobre Oxandrolona!!

Posibles efectos secundarios de los esteroides anabólicos, otras substancias y suplementos usados por atletas. Calvicie, estres en el higado, disfunción eréctil, depresión, acné.

Todo Sobre Oxandrolona!!

Notapor dualoz » Dom Abr 10, 2011 9:39 pm

hola a todos un abrazo fuerte les comento voy a empezar un ciclo de somatropina y Oxa.(segundo ciclo) por lo que me he dado a la tarea de buscar todos los efectos y lo que m preocupa es que muchas veces en unos foros dicen unas cosas y en algunos otros se contradicen pero en fin.. no me salgo del tema retomando, a mi opinion personal este es la mejor informacion que he podido recaudar (via online) para que todos puedan informarse. les dejo el Link http://www.drugs.com/pro/oxandrolone.html y a continuacion les pego la informacion un saludo y suerte en todos sus ciclos! ;)

Oxandrolone
Dosage Form: tablet
-------
BOXED WARNINGS
PELIOSIS HEPATIS, A CONDITION IN WHICH LIVER AND SOMETIMES SPLENIC TISSUE IS REPLACED WITH BLOOD-FILLED CYSTS, HAS BEEN REPORTED IN PATIENTS RECEIVING ANDROGENIC ANABOLIC STEROID THERAPY. THESE CYSTS ARE SOMETIMES PRESENT WITH MINIMAL HEPATIC DYSFUNCTION, BUT AT OTHER TIMES THEY HAVE BEEN ASSOCIATED WITH LIVER FAILURE. THEY ARE OFTEN NOT RECOGNIZED UNTIL LIFE-THREATENING LIVER FAILURE OR INTRA-ABDOMINAL HEMORRHAGE DEVELOPS. WITHDRAWAL OF DRUG USUALLY RESULTS IN COMPLETE DISAPPEARANCE OF LESIONS. LIVER CELL TUMORS ARE ALSO REPORTED. MOST OFTEN THESE TUMORS ARE BENIGN AND ANDROGEN-DEPENDENT, BUT FATAL MALIGNANT TUMORS HAVE BEEN REPORTED. WITHDRAWAL OF DRUG OFTEN RESULTS IN REGRESSION OR CESSATION OF PROGRESSION OF THE TUMOR. HOWEVER, HEPATIC TUMORS ASSOCIATED WITH ANDROGENS OR ANABOLIC STEROIDS ARE MUCH MORE VASCULAR THAN OTHER HEPATIC TUMORS AND MAY BE SILENT UNTIL LIFE-THREATENING INTRA-ABDOMINAL HEMORRHAGE DEVELOPS. BLOOD LIPID CHANGES THAT ARE KNOWN TO BE ASSOCIATED WITH INCREASED RISK OF ATHEROSCLEROSIS ARE SEEN IN PATIENTS TREATED WITH ANDROGENS OR ANABOLIC STEROIDS. THESE CHANGES INCLUDE DECREASED HIGH-DENSITY LIPOPROTEINS AND SOMETIMES INCREASED LOW-DENSITY LIPOPROTEINS. THE CHANGES MAY BE VERY MARKED AND COULD HAVE A SERIOUS IMPACT ON THE RISK OF ATHEROSCLEROSIS AND CORONARY ARTERY DISEASE.

-----

Oxandrolone Description
Oxandrolone oral tablets contain 2.5 mg or 10 mg of the anabolic steroid Oxandrolone. Oxandrolone is 17b-hydroxy-17a-methyl-2-oxa-5a-androstan-3-one with the following structural formula


Molecular Formula: C19H30O3

Molecular Weight: 306.44

Inactive ingredients include: corn starch, lactose monohydrate, magnesium stearate, and hypromellose. USP Dissolution Test Pending.

Oxandrolone - Clinical Pharmacology
Anabolic steroids are synthetic derivatives of testosterone. Certain clinical effects and adverse reactions demonstrate the androgenic properties of this class of drugs. Complete dissociation of anabolic and androgenic effects has not been achieved. The actions of anabolic steroids are therefore similar to those of male sex hormones with the possibility of causing serious disturbances of growth and sexual development if given to young children. Anabolic steroids suppress the gonadotropic functions of the pituitary and may exert a direct effect upon the testes.

During exogenous administration of anabolic androgens, endogenous testosterone release is inhibited through inhibition of pituitary luteinizing hormone (LH). At large doses, spermatogenesis may be suppressed through feedback inhibition of pituitary follicle-stimulating hormone (FSH).

Anabolic steroids have been reported to increase low-density lipoproteins and decrease high-density lipoproteins. These levels revert to normal on discontinuation of treatment.

Indications and Usage for Oxandrolone
Oxandrolone is indicated as adjunctive therapy to offset the protein catabolism associated with prolonged administration of corticosteroids, and for the relief of the bone pain frequently accompanying osteoporosis (see DOSAGE AND ADMINISTRATION).

Drug Abuse and Dependence
Oxandrolone is classified as a controlled substance under the Anabolic Steroids Control Act of 1990 and has been assigned to Schedule III (non-narcotic).

Contraindications
1.Known or suspected carcinoma of the prostate or the male breast.
2.Carcinoma of the breast in females with hypercalcemia (androgenic anabolic steroids may stimulate osteolytic bone resorption).
3.Pregnancy, because of possible masculinization of the fetus. Oxandrolone has been shown to cause embryotoxicity, fetotoxicity, infertility, and masculinization of female animal offspring when given in doses 9 times the human dose.
4.Nephrosis, the nephrotic phase of nephritis.
5.Hypercalcemia.
Warnings
Cholestatic hepatitis and jaundice may occur with 17-alpha-alkylated androgens at a relatively low dose. If cholestatic hepatitis with jaundice appears or if liver function tests become abnormal, Oxandrolone should be discontinued and the etiology should be determined. Drug-induced jaundice is reversible when the medication is discontinued.

In patients with breast cancer, anabolic steroid therapy may cause hypercalcemia by stimulating osteolysis. Oxandrolone therapy should bediscontinued if hypercalcemia occurs.

Edema with or without congestive heart failure may be a serious complication in patients with pre-existing cardiac, renal, or hepatic disease. Concomitant administration of adrenal cortical steroid or ACTH may increase the edema.

In children, androgen therapy may accelerate bone maturation without producing compensatory gain in linear growth. This adverse effect results in compromised adult height. The younger the child, the greater the risk of compromising final mature height. The effect on bone maturation should be monitored by assessing bone age of the left wrist and hand every 6 months (see PRECAUTIONS, LaboratoryTests).

Geriatric patients treated with androgenic anabolic steroids may be at an increased risk for the development of prostatic hypertrophy and prostatic carcinoma. ANABOLIC STEROIDS HAVE NOT BEEN SHOWN TO ENHANCE ATHLETIC ABILITY.

Precautions
Concurrent dosing of Oxandrolone and warfarin may result in unexpectedly large increases in the International Normalized Ratio (INR) or prothrombin time (PT). When Oxandrolone is prescribed to patients being treated with warfarin, doses of warfarin may need to be decreased significantly to maintain the desirable INR level and diminish the risk of potentially serious bleeding (see PRECAUTIONS, Drug Interactions).

General
Women should be observed for signs of virilization (deepening of the voice, hirsutism, acne, clitoromegaly). Discontinuation of drug therapy at the time of evidence of mild virilism is necessary to prevent irreversible virilization. Some virilizing changes in women are irreversible even after prompt discontinuance of therapy and are not prevented by concomitant use of estrogens. Menstrual irregularities may also occur.

Anabolic steroids may cause suppression of clotting factors II, V, VII, and X, and an increase in prothrombin time.

Information for Patients
The physician should instruct patients to report immediately any use of warfarin and any bleeding.

The physician should instruct patients to report any of the following side effects of androgens:

Males:
Too frequent or persistent erections of the penis, appearance or aggravation of acne.

Females:
Hoarseness, acne, changes in menstrual periods, or more facial hair.

All patients:
Nausea, vomiting, changes in skin color, or ankle swelling.

Geriatric Use:
Certain geriatric use information is protected by marketing exclusivity.

Laboratory Tests
Women with disseminated breast carcinoma should have frequent determination of urine and serum calcium levels during the course of therapy (see WARNINGS).

Because of the hepatotoxicity associated with the use of 17-alpha-alkylated androgens, liver function tests should be obtained periodically.

Periodic (every 6 months) x-ray examinations of bone age should be made during treatment of children to determine the rate of bone maturation and the effects of androgen therapy on the epiphyseal centers.

Androgenic anabolic steroids have been reported to increase low-density lipoproteins and decrease high-density lipoproteins. Therefore, caution is required when administering these agents to patients with a history of cardiovascular disease or who are at risk for cardiovascular disease. Serum determination of lipid levels should be performed periodically and therapy adjusted accordingly.

Hemoglobin and hematocrit should be checked periodically for polycythemia in patients who are receiving high doses of anabolic steroids.

Drug Interactions
Anticoagulants:
Anabolic steroids may increase sensitivity to oral anticoagulants. Dosage of the anticoagulant may have to be decreased in order to maintain desired prothrombin time. Patients receiving oral anticoagulant therapy require close monitoring, especially when anabolic steroids are started or stopped.

Warfarin:
A multidose study of Oxandrolone, given as 5 or 10 mg BID in 15 healthy subjects concurrently treated with warfarin, resulted in a mean increase in S-warfarin half-life from 26 to 48 hours and AUC from 4.55 to 12.08 ng•hr/mL; similar increases in R-warfarin half-life and AUC were also detected. Microscopic hematuria (9/15) and gingival bleeding (1/15) were also observed. A 5.5-fold decrease in the mean warfarin dose from 6.13 mg/day to 1.13 mg/day (approximately 80-85% reduction of warfarin dose), was necessary to maintain a target INR of 1.5. When Oxandrolone therapy is initiated in a patient already receiving treatment with warfarin, the INR or prothrombin time (PT) should be monitored closely and the dose of warfarin adjusted as necessary until a stable target INR or PT has been achieved.

Furthermore, in patients receiving both drugs, careful monitoring of the INR or PT, and adjustment of the warfarin dosage if indicated are recommended when the Oxandrolone dose is changed or discontinued. Patients should be closely monitored for signs and symptoms of occult bleeding.

Oral Hypoglycemic Agents:
Oxandrolone may inhibit the metabolism of oral hypoglycemic agents.

Adrenal Steroids or ACTH:
In patients with edema, concomitant administration with adrenal cortical steroids or ACTH may increase the edema.

Drug/Laboratory Test Interactions
Anabolic steroids may decrease levels of thyroxine-binding globulin, resulting in decreased total T4 serum levels and increased resin uptake of T3 and T4. Free thyroid hormone levels remain unchanged. In addition, a decrease in PBI and radioactive iodine uptake may occur.

Carcinogenesis, Mutagenesis, Impairment of Fertility
Animal Data:
Oxandrolone has not been tested in laboratory animals for carcinogenic or mutagenic effects. In 2-year chronic oral rat studies, a dose-related reduction of spermatogenesis and decreased organ weights (testes, prostate, seminal vesicles, ovaries, uterus, adrenals, and pituitary) were shown.

Human Data:
Liver cell tumors have been reported in patients receiving long-term therapy with androgenic anabolic steroids in high doses (see WARNINGS). Withdrawal of the drugs did not lead to regression of the tumors in all cases.

Geriatric patients treated with androgenic anabolic steroids may be at an increased risk for the development of prostatic hypertrophy and prostatic carcinoma.

Pregnancy
Teratogenic effects-Pregnancy Category X (see CONTRAINDICATIONS).

Nursing Mothers
It is not known whether anabolic steroids are excreted in human milk. Because of the potential of serious adverse reactions in nursing infants from Oxandrolone, a decision should be made whether to discontinue nursing or to discontinue the drug, taking into account the importance of the drug to the mother.

Pediatric Use
Anabolic agents may accelerate epiphyseal maturation more rapidly than linear growth in children and the effect may continue for 6 months after the drug has been stopped. Therefore, therapy should be monitored by x-ray studies at 6-month intervals in order to avoid the risk of compromising adult height. Androgenic anabolic steroid therapy should be used very cautiously in children and only by specialists who are aware of the effects on bone maturation (see WARNINGS).

Adverse Reactions
Patients with moderate to severe COPD or COPD patients who are unresponsive to bronchodilators should be monitored closely for COPD exacerbation and fluid retention.

The following adverse reactions have been associated with use of anabolic steroids:

Hepatic
Cholestatic jaundice with, rarely, hepatic necrosis and death. Hepatocellular neoplasms and peliosis hepatis with long-term therapy (see WARNINGS). Reversible changes in liver function tests also occur including increased bromsulfophthalein (BSP) retention, changes in alkaline phosphatase and increases in serum bilirubin, aspartate aminotransferase (AST, SGOT) and alanine aminotransferase (ALT, SGPT).

In Males
Prepubertal:
Phallic enlargement and increased frequency or persistence of erections.

Postpubertal:
Inhibition of testicular function, testicular atrophy and oligospermia, impotence, chronic priapism, epididymitis, and bladder irritability.

In Females
Clitoral enlargement, menstrual irregularities.

CNS
Habituation, excitation, insomnia, depression, and changes in libido.

Hematologic
Bleeding in patients on concomitant anticoagulant therapy.

Breast
Gynecomastia.

Larynx
Deepening of the voice in females.

Hair
Hirsutism and male pattern baldness in females.

Skin
Acne (especially in females and prepubertal males).

Skeletal
Premature closure of epiphyses in children (see PRECAUTIONS, Pediatric Use).

Fluid and Electrolytes
Edema, retention of serum electrolytes (sodium chloride, potassium, phosphate, calcium).

Metabolic/Endocrine
Decreased glucose tolerance (see PRECAUTIONS, Laboratory Tests), increased creatinine excretion, increased serum levels of creatinine phosphokinase (CPK). Masculinization of the fetus. Inhibition of gonadotropin secretion.

Overdosage
No symptoms or signs associated with overdosage have been reported. It is possible that sodium and water retention may occur.

The oral LD50 of Oxandrolone in mice and dogs is greater than 5,000 mg/kg. No specific antidote is known, but gastric lavage may be used.

Oxandrolone Dosage and Administration
Therapy with anabolic steroids is adjunctive to and not a replacement for conventional therapy. The duration of therapy with Oxandrolone will depend on the response of the patient and the possible appearance of adverse reactions. Therapy should be intermittent.

Adults
The response of individuals to anabolic steroids varies. The daily adult dosage is 2.5 mg to 20 mg given in 2 to 4 divided doses. The desired response may be achieved with as little as 2.5 mg or as much as 20 mg daily. A course of therapy of 2 to 4 weeks is usually adequate. This may be repeated intermittently as indicated.

Children
For children the total daily dosage of Oxandrolone is <0.1 mg per kilogram body weight or <0.045 mg per pound of body weight. This may be repeated intermittently as indicated.

How is Oxandrolone Supplied
Oxandrolone Tablets, USP are supplied as follows:

2.5 mg tablets: white, round, biconvex tablets, debossed with “K” and scored on one side and “200” on the other side.

Bottles of 100 (NDC 49884-301-01)

10 mg tablets: white, capsule shaped, biconvex tablets, debossed with “201” on one side and debossed with “K” on the other side.

Bottles of 60 (NDC 49884-302-02)

Store at 20°-25° C (68°-77°F) [see USP Controlled Room Temperature].

Manufactured by:

Par Pharmaceutical Companies, Inc.

Spring Valley, NY 10977

Revised: 11/09

OS301-01-1-03

DISPLAY PANEL, 2.5 MG 100 TABLETS

DISPLAY PANEL 10 MG 60 TABLETS


Oxandrolone
Oxandrolone tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG NDC Product Code (Source) 49884-301
Route of Administration ORAL DEA Schedule CIII

Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Oxandrolone (Oxandrolone) Oxandrolone 2.5 mg

Inactive Ingredients
Ingredient Name Strength
LACTOSE MONOHYDRATE
STARCH, CORN
HYPROMELLOSE
MAGNESIUM STEARATE

Product Characteristics
Color WHITE Score 2 pieces
Shape ROUND Size 7mm
Flavor Imprint Code K200
Contains

Packaging
# NDC Package Description Multilevel Packaging
1 49884-301-01 100 TABLET In 1 BOTTLE, PLASTIC None


Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA077827 08/20/2007

Oxandrolone
Oxandrolone tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG NDC Product Code (Source) 49884-302
Route of Administration ORAL DEA Schedule CIII

Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Oxandrolone (Oxandrolone) Oxandrolone 10 mg

Inactive Ingredients
Ingredient Name Strength
LACTOSE MONOHYDRATE
STARCH, CORN
HYPROMELLOSE
MAGNESIUM STEARATE

Product Characteristics
Color WHITE Score no score
Shape CAPSULE (BICONVEX) Size 16mm
Flavor Imprint Code K201
Contains

Packaging
# NDC Package Description Multilevel Packaging
1 49884-302-02 60 TABLET In 1 BOTTLE, PLASTIC None


Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA077827 08/20/2007

Labeler - Par Pharmaceutical Inc. (092733690)
Registrant - Par Pharmaceutical Inc. (092733690)
Revised: 07/2010Par Pharmaceutical Inc.
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Mensajes: 11
Registrado: Vie Ago 13, 2010 9:26 pm





Re: Todo Sobre Oxandrolona!!

Notapor jrd25 » Mié Abr 13, 2011 5:03 pm

dualoz escribió:hola a todos un abrazo fuerte les comento voy a empezar un ciclo de somatropina y Oxa.(segundo ciclo) por lo que me he dado a la tarea de buscar todos los efectos y lo que m preocupa es que muchas veces en unos foros dicen unas cosas y en algunos otros se contradicen pero en fin.. no me salgo del tema retomando, a mi opinion personal este es la mejor informacion que he podido recaudar (via online) para que todos puedan informarse. les dejo el Link http://www.drugs.com/pro/oxandrolone.html y a continuacion les pego la informacion un saludo y suerte en todos sus ciclos! ;)

Oxandrolone
Dosage Form: tablet
-------
BOXED WARNINGS
PELIOSIS HEPATIS, A CONDITION IN WHICH LIVER AND SOMETIMES SPLENIC TISSUE IS REPLACED WITH BLOOD-FILLED CYSTS, HAS BEEN REPORTED IN PATIENTS RECEIVING ANDROGENIC ANABOLIC STEROID THERAPY. THESE CYSTS ARE SOMETIMES PRESENT WITH MINIMAL HEPATIC DYSFUNCTION, BUT AT OTHER TIMES THEY HAVE BEEN ASSOCIATED WITH LIVER FAILURE. THEY ARE OFTEN NOT RECOGNIZED UNTIL LIFE-THREATENING LIVER FAILURE OR INTRA-ABDOMINAL HEMORRHAGE DEVELOPS. WITHDRAWAL OF DRUG USUALLY RESULTS IN COMPLETE DISAPPEARANCE OF LESIONS. LIVER CELL TUMORS ARE ALSO REPORTED. MOST OFTEN THESE TUMORS ARE BENIGN AND ANDROGEN-DEPENDENT, BUT FATAL MALIGNANT TUMORS HAVE BEEN REPORTED. WITHDRAWAL OF DRUG OFTEN RESULTS IN REGRESSION OR CESSATION OF PROGRESSION OF THE TUMOR. HOWEVER, HEPATIC TUMORS ASSOCIATED WITH ANDROGENS OR ANABOLIC STEROIDS ARE MUCH MORE VASCULAR THAN OTHER HEPATIC TUMORS AND MAY BE SILENT UNTIL LIFE-THREATENING INTRA-ABDOMINAL HEMORRHAGE DEVELOPS. BLOOD LIPID CHANGES THAT ARE KNOWN TO BE ASSOCIATED WITH INCREASED RISK OF ATHEROSCLEROSIS ARE SEEN IN PATIENTS TREATED WITH ANDROGENS OR ANABOLIC STEROIDS. THESE CHANGES INCLUDE DECREASED HIGH-DENSITY LIPOPROTEINS AND SOMETIMES INCREASED LOW-DENSITY LIPOPROTEINS. THE CHANGES MAY BE VERY MARKED AND COULD HAVE A SERIOUS IMPACT ON THE RISK OF ATHEROSCLEROSIS AND CORONARY ARTERY DISEASE.

-----

Oxandrolone Description
Oxandrolone oral tablets contain 2.5 mg or 10 mg of the anabolic steroid Oxandrolone. Oxandrolone is 17b-hydroxy-17a-methyl-2-oxa-5a-androstan-3-one with the following structural formula


Molecular Formula: C19H30O3

Molecular Weight: 306.44

Inactive ingredients include: corn starch, lactose monohydrate, magnesium stearate, and hypromellose. USP Dissolution Test Pending.

Oxandrolone - Clinical Pharmacology
Anabolic steroids are synthetic derivatives of testosterone. Certain clinical effects and adverse reactions demonstrate the androgenic properties of this class of drugs. Complete dissociation of anabolic and androgenic effects has not been achieved. The actions of anabolic steroids are therefore similar to those of male sex hormones with the possibility of causing serious disturbances of growth and sexual development if given to young children. Anabolic steroids suppress the gonadotropic functions of the pituitary and may exert a direct effect upon the testes.

During exogenous administration of anabolic androgens, endogenous testosterone release is inhibited through inhibition of pituitary luteinizing hormone (LH). At large doses, spermatogenesis may be suppressed through feedback inhibition of pituitary follicle-stimulating hormone (FSH).

Anabolic steroids have been reported to increase low-density lipoproteins and decrease high-density lipoproteins. These levels revert to normal on discontinuation of treatment.

Indications and Usage for Oxandrolone
Oxandrolone is indicated as adjunctive therapy to offset the protein catabolism associated with prolonged administration of corticosteroids, and for the relief of the bone pain frequently accompanying osteoporosis (see DOSAGE AND ADMINISTRATION).

Drug Abuse and Dependence
Oxandrolone is classified as a controlled substance under the Anabolic Steroids Control Act of 1990 and has been assigned to Schedule III (non-narcotic).

Contraindications
1.Known or suspected carcinoma of the prostate or the male breast.
2.Carcinoma of the breast in females with hypercalcemia (androgenic anabolic steroids may stimulate osteolytic bone resorption).
3.Pregnancy, because of possible masculinization of the fetus. Oxandrolone has been shown to cause embryotoxicity, fetotoxicity, infertility, and masculinization of female animal offspring when given in doses 9 times the human dose.
4.Nephrosis, the nephrotic phase of nephritis.
5.Hypercalcemia.
Warnings
Cholestatic hepatitis and jaundice may occur with 17-alpha-alkylated androgens at a relatively low dose. If cholestatic hepatitis with jaundice appears or if liver function tests become abnormal, Oxandrolone should be discontinued and the etiology should be determined. Drug-induced jaundice is reversible when the medication is discontinued.

In patients with breast cancer, anabolic steroid therapy may cause hypercalcemia by stimulating osteolysis. Oxandrolone therapy should bediscontinued if hypercalcemia occurs.

Edema with or without congestive heart failure may be a serious complication in patients with pre-existing cardiac, renal, or hepatic disease. Concomitant administration of adrenal cortical steroid or ACTH may increase the edema.

In children, androgen therapy may accelerate bone maturation without producing compensatory gain in linear growth. This adverse effect results in compromised adult height. The younger the child, the greater the risk of compromising final mature height. The effect on bone maturation should be monitored by assessing bone age of the left wrist and hand every 6 months (see PRECAUTIONS, LaboratoryTests).

Geriatric patients treated with androgenic anabolic steroids may be at an increased risk for the development of prostatic hypertrophy and prostatic carcinoma. ANABOLIC STEROIDS HAVE NOT BEEN SHOWN TO ENHANCE ATHLETIC ABILITY.

Precautions
Concurrent dosing of Oxandrolone and warfarin may result in unexpectedly large increases in the International Normalized Ratio (INR) or prothrombin time (PT). When Oxandrolone is prescribed to patients being treated with warfarin, doses of warfarin may need to be decreased significantly to maintain the desirable INR level and diminish the risk of potentially serious bleeding (see PRECAUTIONS, Drug Interactions).

General
Women should be observed for signs of virilization (deepening of the voice, hirsutism, acne, clitoromegaly). Discontinuation of drug therapy at the time of evidence of mild virilism is necessary to prevent irreversible virilization. Some virilizing changes in women are irreversible even after prompt discontinuance of therapy and are not prevented by concomitant use of estrogens. Menstrual irregularities may also occur.

Anabolic steroids may cause suppression of clotting factors II, V, VII, and X, and an increase in prothrombin time.

Information for Patients
The physician should instruct patients to report immediately any use of warfarin and any bleeding.

The physician should instruct patients to report any of the following side effects of androgens:

Males:
Too frequent or persistent erections of the penis, appearance or aggravation of acne.

Females:
Hoarseness, acne, changes in menstrual periods, or more facial hair.

All patients:
Nausea, vomiting, changes in skin color, or ankle swelling.

Geriatric Use:
Certain geriatric use information is protected by marketing exclusivity.

Laboratory Tests
Women with disseminated breast carcinoma should have frequent determination of urine and serum calcium levels during the course of therapy (see WARNINGS).

Because of the hepatotoxicity associated with the use of 17-alpha-alkylated androgens, liver function tests should be obtained periodically.

Periodic (every 6 months) x-ray examinations of bone age should be made during treatment of children to determine the rate of bone maturation and the effects of androgen therapy on the epiphyseal centers.

Androgenic anabolic steroids have been reported to increase low-density lipoproteins and decrease high-density lipoproteins. Therefore, caution is required when administering these agents to patients with a history of cardiovascular disease or who are at risk for cardiovascular disease. Serum determination of lipid levels should be performed periodically and therapy adjusted accordingly.

Hemoglobin and hematocrit should be checked periodically for polycythemia in patients who are receiving high doses of anabolic steroids.

Drug Interactions
Anticoagulants:
Anabolic steroids may increase sensitivity to oral anticoagulants. Dosage of the anticoagulant may have to be decreased in order to maintain desired prothrombin time. Patients receiving oral anticoagulant therapy require close monitoring, especially when anabolic steroids are started or stopped.

Warfarin:
A multidose study of Oxandrolone, given as 5 or 10 mg BID in 15 healthy subjects concurrently treated with warfarin, resulted in a mean increase in S-warfarin half-life from 26 to 48 hours and AUC from 4.55 to 12.08 ng•hr/mL; similar increases in R-warfarin half-life and AUC were also detected. Microscopic hematuria (9/15) and gingival bleeding (1/15) were also observed. A 5.5-fold decrease in the mean warfarin dose from 6.13 mg/day to 1.13 mg/day (approximately 80-85% reduction of warfarin dose), was necessary to maintain a target INR of 1.5. When Oxandrolone therapy is initiated in a patient already receiving treatment with warfarin, the INR or prothrombin time (PT) should be monitored closely and the dose of warfarin adjusted as necessary until a stable target INR or PT has been achieved.

Furthermore, in patients receiving both drugs, careful monitoring of the INR or PT, and adjustment of the warfarin dosage if indicated are recommended when the Oxandrolone dose is changed or discontinued. Patients should be closely monitored for signs and symptoms of occult bleeding.

Oral Hypoglycemic Agents:
Oxandrolone may inhibit the metabolism of oral hypoglycemic agents.

Adrenal Steroids or ACTH:
In patients with edema, concomitant administration with adrenal cortical steroids or ACTH may increase the edema.

Drug/Laboratory Test Interactions
Anabolic steroids may decrease levels of thyroxine-binding globulin, resulting in decreased total T4 serum levels and increased resin uptake of T3 and T4. Free thyroid hormone levels remain unchanged. In addition, a decrease in PBI and radioactive iodine uptake may occur.

Carcinogenesis, Mutagenesis, Impairment of Fertility
Animal Data:
Oxandrolone has not been tested in laboratory animals for carcinogenic or mutagenic effects. In 2-year chronic oral rat studies, a dose-related reduction of spermatogenesis and decreased organ weights (testes, prostate, seminal vesicles, ovaries, uterus, adrenals, and pituitary) were shown.

Human Data:
Liver cell tumors have been reported in patients receiving long-term therapy with androgenic anabolic steroids in high doses (see WARNINGS). Withdrawal of the drugs did not lead to regression of the tumors in all cases.

Geriatric patients treated with androgenic anabolic steroids may be at an increased risk for the development of prostatic hypertrophy and prostatic carcinoma.

Pregnancy
Teratogenic effects-Pregnancy Category X (see CONTRAINDICATIONS).

Nursing Mothers
It is not known whether anabolic steroids are excreted in human milk. Because of the potential of serious adverse reactions in nursing infants from Oxandrolone, a decision should be made whether to discontinue nursing or to discontinue the drug, taking into account the importance of the drug to the mother.

Pediatric Use
Anabolic agents may accelerate epiphyseal maturation more rapidly than linear growth in children and the effect may continue for 6 months after the drug has been stopped. Therefore, therapy should be monitored by x-ray studies at 6-month intervals in order to avoid the risk of compromising adult height. Androgenic anabolic steroid therapy should be used very cautiously in children and only by specialists who are aware of the effects on bone maturation (see WARNINGS).

Adverse Reactions
Patients with moderate to severe COPD or COPD patients who are unresponsive to bronchodilators should be monitored closely for COPD exacerbation and fluid retention.

The following adverse reactions have been associated with use of anabolic steroids:

Hepatic
Cholestatic jaundice with, rarely, hepatic necrosis and death. Hepatocellular neoplasms and peliosis hepatis with long-term therapy (see WARNINGS). Reversible changes in liver function tests also occur including increased bromsulfophthalein (BSP) retention, changes in alkaline phosphatase and increases in serum bilirubin, aspartate aminotransferase (AST, SGOT) and alanine aminotransferase (ALT, SGPT).

In Males
Prepubertal:
Phallic enlargement and increased frequency or persistence of erections.

Postpubertal:
Inhibition of testicular function, testicular atrophy and oligospermia, impotence, chronic priapism, epididymitis, and bladder irritability.

In Females
Clitoral enlargement, menstrual irregularities.

CNS
Habituation, excitation, insomnia, depression, and changes in libido.

Hematologic
Bleeding in patients on concomitant anticoagulant therapy.

Breast
Gynecomastia.

Larynx
Deepening of the voice in females.

Hair
Hirsutism and male pattern baldness in females.

Skin
Acne (especially in females and prepubertal males).

Skeletal
Premature closure of epiphyses in children (see PRECAUTIONS, Pediatric Use).

Fluid and Electrolytes
Edema, retention of serum electrolytes (sodium chloride, potassium, phosphate, calcium).

Metabolic/Endocrine
Decreased glucose tolerance (see PRECAUTIONS, Laboratory Tests), increased creatinine excretion, increased serum levels of creatinine phosphokinase (CPK). Masculinization of the fetus. Inhibition of gonadotropin secretion.

Overdosage
No symptoms or signs associated with overdosage have been reported. It is possible that sodium and water retention may occur.

The oral LD50 of Oxandrolone in mice and dogs is greater than 5,000 mg/kg. No specific antidote is known, but gastric lavage may be used.

Oxandrolone Dosage and Administration
Therapy with anabolic steroids is adjunctive to and not a replacement for conventional therapy. The duration of therapy with Oxandrolone will depend on the response of the patient and the possible appearance of adverse reactions. Therapy should be intermittent.

Adults
The response of individuals to anabolic steroids varies. The daily adult dosage is 2.5 mg to 20 mg given in 2 to 4 divided doses. The desired response may be achieved with as little as 2.5 mg or as much as 20 mg daily. A course of therapy of 2 to 4 weeks is usually adequate. This may be repeated intermittently as indicated.

Children
For children the total daily dosage of Oxandrolone is <0.1 mg per kilogram body weight or <0.045 mg per pound of body weight. This may be repeated intermittently as indicated.

How is Oxandrolone Supplied
Oxandrolone Tablets, USP are supplied as follows:

2.5 mg tablets: white, round, biconvex tablets, debossed with “K” and scored on one side and “200” on the other side.

Bottles of 100 (NDC 49884-301-01)

10 mg tablets: white, capsule shaped, biconvex tablets, debossed with “201” on one side and debossed with “K” on the other side.

Bottles of 60 (NDC 49884-302-02)

Store at 20°-25° C (68°-77°F) [see USP Controlled Room Temperature].

Manufactured by:

Par Pharmaceutical Companies, Inc.

Spring Valley, NY 10977

Revised: 11/09

OS301-01-1-03

DISPLAY PANEL, 2.5 MG 100 TABLETS

DISPLAY PANEL 10 MG 60 TABLETS


Oxandrolone
Oxandrolone tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG NDC Product Code (Source) 49884-301
Route of Administration ORAL DEA Schedule CIII

Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Oxandrolone (Oxandrolone) Oxandrolone 2.5 mg

Inactive Ingredients
Ingredient Name Strength
LACTOSE MONOHYDRATE
STARCH, CORN
HYPROMELLOSE
MAGNESIUM STEARATE

Product Characteristics
Color WHITE Score 2 pieces
Shape ROUND Size 7mm
Flavor Imprint Code K200
Contains

Packaging
# NDC Package Description Multilevel Packaging
1 49884-301-01 100 TABLET In 1 BOTTLE, PLASTIC None


Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA077827 08/20/2007

Oxandrolone
Oxandrolone tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG NDC Product Code (Source) 49884-302
Route of Administration ORAL DEA Schedule CIII

Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Oxandrolone (Oxandrolone) Oxandrolone 10 mg

Inactive Ingredients
Ingredient Name Strength
LACTOSE MONOHYDRATE
STARCH, CORN
HYPROMELLOSE
MAGNESIUM STEARATE

Product Characteristics
Color WHITE Score no score
Shape CAPSULE (BICONVEX) Size 16mm
Flavor Imprint Code K201
Contains

Packaging
# NDC Package Description Multilevel Packaging
1 49884-302-02 60 TABLET In 1 BOTTLE, PLASTIC None


Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA077827 08/20/2007

Labeler - Par Pharmaceutical Inc. (092733690)
Registrant - Par Pharmaceutical Inc. (092733690)
Revised: 07/2010Par Pharmaceutical Inc.


Gracias por el aporte, tiene muy buena pinta, lastima que mis conocicmientos con el ingles sean bajos....
Yo tambien usasre oxa de salida en mi proximo ciclo...espero obtener buenos resultados!!!

Suerte!!
-Grandes descubrimientos y mejoras implican invariablemente la cooperación de muchas mentes.
-La costancia es la clave del exito
-"No pain, no gain"

f-a-q-para-los-nuevos-importante-t2992.html

ciclos-basicos-t31742.html
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jrd25
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Mensajes: 256
Registrado: Dom Sep 19, 2010 10:52 am

Re: Todo Sobre Oxandrolona!!

Notapor Aytosh » Sab Abr 16, 2011 4:58 pm

no me gusto oxandrolona. es muy caro y un poco efectivo
hola amigos. soy de Turquia y estoy aprendiendo espanol.
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Aytosh
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Mensajes: 756
Registrado: Mié Feb 24, 2010 3:03 pm

Re: Todo Sobre Oxandrolona!!

Notapor jrd25 » Dom Abr 17, 2011 1:16 pm

Aytosh escribió:no me gusto oxandrolona. es muy caro y un poco efectivo


Oxa hay mucha que es fake debido a su escasez y al ser un buen quimico...que oxa tomaste???puede que fuese fake o no tomaras la cantidad adecuada....

Saludos!!!
-Grandes descubrimientos y mejoras implican invariablemente la cooperación de muchas mentes.
-La costancia es la clave del exito
-"No pain, no gain"

f-a-q-para-los-nuevos-importante-t2992.html

ciclos-basicos-t31742.html
Avatar de Usuario
jrd25
Forista Senior
Forista Senior
 
Mensajes: 256
Registrado: Dom Sep 19, 2010 10:52 am

Re: Todo Sobre Oxandrolona!!

Notapor Aytosh » Dom Abr 17, 2011 3:42 pm

jrd25 escribió:
Aytosh escribió:no me gusto oxandrolona. es muy caro y un poco efectivo


Oxa hay mucha que es fake debido a su escasez y al ser un buen quimico...que oxa tomaste???puede que fuese fake o no tomaras la cantidad adecuada....

Saludos!!!

genesis. tomo 40 mg sin efecto de kick start. tengo otros amigos que tomo oxa de otro labs con muy poco o no efectos
hola amigos. soy de Turquia y estoy aprendiendo espanol.
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Aytosh
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Mensajes: 756
Registrado: Mié Feb 24, 2010 3:03 pm

Re: Todo Sobre Oxandrolona!!

Notapor Ecko72 » Dom Abr 17, 2011 9:48 pm

Oxandrolona es un esteroide para mujeres,se necesita de dosis altas (+40mg) para tener efectos notables,por lo gral. se usa de salida o al final pero siempre dentro de un ciclo no como monociclo.

Los perfiles que mencionas son buenos pero en si el farmaco esta diseñado para mujeres :( no hay ganancias remarcables.
Ecko72
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Mensajes: 12732
Registrado: Dom Feb 25, 2007 10:21 pm
Ubicación: Mexico

Re: Todo Sobre Oxandrolona!!

Notapor solbergpp » Mar Jun 19, 2012 10:18 am

buenisimo el post, lo único que le falto en los warnings la precaución en Alérgicos a penisilina y colorantes, ya que la oxandrolona puede tener una reacción cruzada en este tipo de personas.
solbergpp
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