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Indications

REMS


Contraind./Precautions

Contraindicated in:

Use Cautiously in:

Adv. Reactions/Side Effects

CV: edema, hypertension

Derm: hot flashes, acne

EENT: nasal irritation (nasal spray)

Endo: glucose intolerance, gynecomastia, testosterone flare

GI: constipation, nausea

GU: libido, menorrhagia, vaginal dryness, impotence, suppression of ovulation

Hemat: anemia

Local: injection site reactions

MS: bone pain, osteoporosis

Neuro: headache (nasal spray), insomnia, weakness, depression, dizziness

Misc: transient exacerbation of metastatic prostate cancer or endometriosis

Interactions

Drug-drug:

Availability

Route/Dosage

Prostate cancer

Endometriosis

Action

  • Acts as a synthetic analog of endogenous gonadotropin-releasing hormone (GnRH/LHRH). Chronic use results in inhibited secretion of gonadotropin release and gonadal steroid production. The overall effect is due to downregulation of pituitary LHRH receptors. In men, testosterone synthesis and release are . In women, secretion of estrogen is .
Therapeutic effects:
  • Decreased spread of advanced prostate cancer.
  • Decreased sequelae of endometriosis (pain, dysmenorrhea).

Classifications

Therapeutic Classification: antineoplastics, hormones

Pharmacologic Classification: luteinizing hormone-releasing hormone (LHRH) analogues

Pharmacokinetics

Absorption: SUBQ: 70%; intranasal: 1–3%; implant: drug is slowly absorbed over 2–3 mo.

Distribution: Accumulates in liver, kidneys and anterior pituitary lobe.

Metabolism/Excretion: Metabolized in liver and kidneys and by enzymes on membranes in the pituitary gland.

Half-Life: SUBQ: 80 min; intranasal: 1–2 hr; implant: 20–30 days.

Canadian Brand Names

Suprefact

Time/Action Profile

ROUTEONSETPEAKDURATION
prostate cancer 7 days4 mountil discontinuation
endometriosis (intranasal)unknownunknownduration of treatment

in testosterone concentrations.

Symptom improvement.

Patient/Family Teaching

Pronunciation

bue-se-REL-in