Octreotide
SANDOSTATIN LAR DEPOT is a somatostatin analogue indicated for: Treatment in patients who have responded to and tolerated Sandostatin Injection subcutaneous injection for:
•Acromegaly.
•Severe diarrhea/flushing episodes associated with metastatic carcinoid tumors.
•Profuse watery diarrhea associated with Vasoactive Intestinal Peptide (VIP) secreting tumors.
Patients not currently receiving Sandostatin Injection subcutaneously:
•Acromegaly: 50 mcg three times daily Sandostatin Injection subcutaneously for 2 weeks followed by SANDOSTATIN LAR DEPOT 20 mg intragluteally every 4 weeks for 3 months.
•Carcinoid Tumors and VIPomas: Sandostatin Injection subcutaneously 100-600 mcg/day in 2-4 divided doses for 2 weeks followed by SANDOSTATIN LAR DEPOT 20 mg every 4 weeks for 2 months. See package insert for complete information.
The most common adverse reactions, occurring in ≥ 20% of patients are:
•Acromegaly: diarrhea, cholelithiasis, abdominal pain, flatulence.
•Carcinoid Syndrome: back pain, fatigue, headache, abdominal pain, nausea, dizziness.
• Cholelithiasis and Complications of Cholelithiasis. Monitor periodically. Discontinue if complications of cholelithiasis are suspected. •Glucose Metabolism: Hypoglycemia or hyperglycemia may occur. Glucose monitoring is recommended and antidiabetic treatment may need adjustment.
•Thyroid Function: Hypothyroidism may occur. Monitor thyroid levels periodically.
•Cardiac Function: Bradycardia, arrhythmia, or conduction abnormalities may occur. Use with caution in at-risk patients.