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Androgel 1.62% Generic Name & Formulations
Legal Class
CIII
General Description
Testosterone 1.62% (20.25mg of testosterone per one pump actuation); gel.
Pharmacological Class
Androgen.
See Also
How Supplied
Gel 1% (2.5g, 5g)—contact supplier; Gel 1.62% (60 metered 1.25g doses)—1
Manufacturer
Generic Availability
Gel 1.62% (YES)
Androgel 1.62% Indications
Indications
Testosterone replacement therapy in adult males with congenital or acquired primary hypogonadism or hypogonadotropic hypogonadism.
Limitations of Use
Not established in men with age-related hypogonadism.
Androgel 1.62% Dosage and Administration
Adult
Advise patients to strictly adhere to recommended instructions. Apply to clean, intact, dry skin of the shoulders and upper arms; do not apply to abdomen, genitals, chest, axillae, or knees. ≥18yrs: 2.5g (40.5mg of testosterone [2 pump actuations]) once daily in the AM. May adjust dose between minimum of 20.25mg (1 pump actuation) and a maximum of 81mg (4 pump actuations) based on the pre-dose morning serum testosterone concentration at approx. 14 days and 28 days after starting treatment or following dose adjustment. See full labeling. Check additional serum testosterone levels periodically thereafter. Wash hands after application. Allow gel to dry before it touches clothing.
Children
<18yrs: not established.
Androgel 1.62% Contraindications
Contraindications
Male breast or prostate cancer. Pregnant women (must avoid skin contact with application sites in men). Nursing mothers.
Androgel 1.62% Boxed Warnings
Boxed Warning
Secondary exposure to testosterone.
Androgel 1.62% Warnings/Precautions
Warnings/Precautions
Not for use in women. Not interchangeable with other topical testosterone products. Other persons (esp. children) must avoid contact with application site. Secondary exposure to testosterone; promptly discontinue if signs of virilization in children and women occurs, until cause is identified. Increased risk for worsening BPH; monitor for signs/symptoms. Evaluate for prostate cancer before starting therapy. Preexisting cardiac, renal, or hepatic disease (discontinue if edema occurs). May worsen sleep apnea. Monitor hematocrit prior to initiation, at 3–6 months after starting therapy, then annually; if elevation occurs, withhold until acceptable level. Testosterone and/or other anabolic androgenic steroid abuse. Monitor serum testosterone, PSA, liver function, cholesterol, lipid profile, serum calcium (in cancer patients at risk for hypercalcemia). Monitor for venous thromboembolism; discontinue if suspected. Inform patients of possible increased risk of MI, stroke. Flammable. Elderly.
REMS
Androgel 1.62% Pharmacokinetics
See Literature
Androgel 1.62% Interactions
Interactions
May alter insulin sensitivity and glycemic control; reduce dose of antidiabetic agents if needed. Increased fluid retention with concomitant ACTH, corticosteroids; monitor. Monitor INR and PT with concomitant oral anticoagulants. May affect thyroid levels.
Androgel 1.62% Adverse Reactions
Adverse Reactions
Acne, local reactions, lab abnormalities, prostate disorders, increased PSA, emotional lability, hypertension, breast pain, gynecomastia, nervousness, testis disorders; edema, virilization in children.
Androgel 1.62% Clinical Trials
See Literature
Androgel 1.62% Note
Not Applicable
Androgel 1.62% Patient Counseling
See Literature
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