lanreotide
(lan-ree-o-tide)
Somatuline Depot

Classification
Therapeutic: hormones
Pharmacologic: somatostatin analogues

Pregnancy Category C


Copyright © 2007 by F.A. Davis Company

Indications
Long-term management of acromegaly which cannot be treated by or has not responded to surgery and/or radiation therapy.

Action
Acts as an analog of somatostatin, inhibiting growth hormone (GH) and insulin-like growth factor-1 (IGF-1) in patients with acromegaly. Therapeutic Effects: Decreased levels of growth hormone (GH) and insulin-like growth factor-1 (IGF-1) in acromegalic patients resulting in decreased manifestations of acromegaly.

Pharmacokinetics
Absorption: Following subcut administration, lanreotide precipitates in body tissues acting as a depot formulation from which drug is slowly released (75% bioavailability).
Distribution: Unknown.
Metabolism and Excretion: Minimal renal/fecal excretion, some biliary excretion.
Half-life: 23–30 days.

TIME/ACTION PROFILE

ROUTEONSETPEAKDURATION
Subcutunknownfirst 24 hr1 mo


Contraindications/Precautions
Contraindicated in: OB: Lactation.
Use Cautiously in: Diabetic patients; Underlying heart disease, especially bradycardia; OB: Use only if maternal benefit outweighs risk to fetus; Pedi: Safe use in children has not been established.

Adverse Reactions/Side Effects*
*CAPITALS indicate life threatening; underlines indicate most frequent.

CV: bradycardia, hypertension. GI: abdominal pain, diarrhea, gallstones. Endo: hyperglycemia, hypoglycemia. Hemat: anemia. Local: injection site reactions.

Interactions
Drug–Drug: ↑ risk of bradycardia with other drugs that may cause ↓ heart rate including beta-blockers. May ↓ absorption of cyclosporine (dose adjustment may be necessary). May alter the effects of antidiabetic agents (monitor blood sugar). May ↓ activity or CYP450 enzyme system, use cautiously with drugs metabolized by that system, including quinidine.

Route/Dosage
Subcut (Adults): 90 mg every 4 week for 3 mos, further adjustments are made on the basis of GH and IGF1 levels as follows: GH > 1 to £2.5 ng/mL, IGF-1 normal with good symptom control— maintain dose at 90 mg every 4 wk;GH >2.5 ng/mL, IGF-1 elevated and/or uncontrolled symptoms— increase to 120 mg every 4 wk; GH £1 mg/mL, IGF-1 symptoms currently controlled—decrease dose to 60 mg every 4 wk.
Renal/Hepatic Impairment
Subcut (Adults): Moderate to severe hepatic or renal impairment— 60 mg every 4 wk; further adjustments are made on the basis of Growth Hormone (GH) and insulin growth factor-1(IGF1) levels.


Availability
Semi-solid in pre-filled syringes: 60 mg, 90 mg, 120 mg.

NURSING IMPLICATIONS

Assessment Potential Nursing Diagnoses
Risk for disproportionate growth (Indications).
Deficient knowledge, related to medication regimen (Patient/Family Teaching).

Implementation Patient/Family Teaching Evaluation/Desired Outcomes


Copyright © 2007 by F.A. Davis Company