Indication

Primary hypogonadism due to orchitis

Primary hypogonadism due to orchitis is an acquired form of male hypergonadotropic hypogonadism characterized by intrinsic testicular failure following severe inflammation or infection of the testes, most commonly viral mumps or severe bacterial epididymo-orchitis. Read more about Primary hypogonadism due to orchitis

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Drugs that treat it

Common Primary hypogonadism due to orchitis therapies.

Showing 55–63 of 106 drugs

TESTOSTERONE

ANDROGENS/ANABOLIC STEROIDS·GONADOTROPIN RELEASING FACTOR DEFICIENCY·+9
CIPLA USA, INC.

TESTOSTERONE CYPIONATE

ANDROGENS/ANABOLIC STEROIDS·GONADOTROPIN RELEASING FACTOR DEFICIENCY·+9
CIPLA USA, INC.

TESTOSTERONE ENANTHATE

ANDROGENS/ANABOLIC STEROIDS·GONADOTROPIN RELEASING FACTOR DEFICIENCY·+11
EMPOWER PHARMAC

TESTOSTERONE ENANTHATE

ANDROGENS/ANABOLIC STEROIDS·GONADOTROPIN RELEASING FACTOR DEFICIENCY·+11
Hikma Pharmaceuticals USA
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About Primary hypogonadism due to orchitis.

Primary hypogonadism due to orchitis is an acquired form of male hypergonadotropic hypogonadism characterized by intrinsic testicular failure following severe inflammation or infection of the testes, most commonly viral mumps or severe bacterial epididymo-orchitis.

The inflammatory injury damages the testicular parenchyma, resulting in destruction or dysfunction of androgen-producing Leydig cells and seminiferous tubules.

Clinically and pathophysiologically, this condition manifests in adult or adolescent males with subnormal circulating testosterone concentrations accompanied by a compensatory elevation in serum gonadotropins, specifically luteinizing hormone and follicle-stimulating hormone.

Affected patients typically present with testicular atrophy, reduced libido, erectile dysfunction, fatigue, and impaired spermatogenesis.

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