Successful preparation and administration of Octreotide Acetate for Injectable Suspension relies on proper suspension technique.
It should only be administered by a trained healthcare provider.
Follow each of the steps outlined in the instruction booklet to ensure complete saturation of the powder and its uniform
suspension prior to deep intragluteal injection. It is critical that Octreotide Acetate for Injectable Suspension and the diluent be allowed to reach room temperature and then be mixed immediately prior to injection.
Ensure that the powder is completely suspended at the time of injection. If you have questions about preparation and/or administration of Octreotide Acetate for Injectable Suspension, please call 1-888-838-2872.
Preparing and Administering Octreotide Acetate for Injectable Suspensions, for gluteal intramuscular use
Octreotide Acetate for Injectable Suspension, for gluteal intramuscular use is available in single-dose kits containing an 8-mL single-dose vial of 10 mg, 20 mg or 30 mg strength, a prefilled syringe containing 2 mL of diluent, one vial adapter, and one sterile 1.5” 19-gauge safety injection needle.
An instruction booklet for the preparation of drug suspension for injection is also included with each kit.
ATTENTION: It is essential to start the reconstitution process only after the injection kit has reached room temperature. Let the kit stand at room temperature for a minimum of 30 minutes before reconstitution, but do not exceed 24 hours.
Note: The injection kit can be re-refrigerated if needed.
ATTENTION: It is essential to let the vial stand for a minimum of 2 minutes and up to 5 minutes to ensure that the diluent has fully saturated the powder.
Note: It is normal if the plunger rod moves up as there might be a slight overpressure in the vial.
ATTENTION: Keep the plunger pressed and shake the vial moderately in a horizontal direction for a minimum of 30 seconds so that the powder is completely suspended (uniform milky suspension). Repeat moderate shaking for another 30 seconds if the powder is not completely suspended.
Special precautions for disposal: any unused product or waste material should be disposed of in accordance with local requirements.
Treatment with octreotide acetate for injectable suspension may affect gallbladder function, with reports of gallstones resulting in complications (inflammation of the gallbladder, bile duct, and pancreas, and requiring surgical removal of the gallbladder); sugar metabolism; thyroid and heart function; stool discoloration and loose stool, which may require monitoring by your doctor. Tell your doctor if you experience signs or symptoms of gallstones or any of their complications.
Patients with carcinoid tumors and VIP-secreting tumors should adhere closely to their scheduled return visits for reinjection in order to minimize exacerbation of symptoms.
Patients with acromegaly should adhere to their return visit schedule to help assure steady control of GH and IGF-1 levels.
Tell your doctor if you have a history of heart disease or are taking other medications, including cyclosporine, insulin, oral hypoglycemic agents, beta-blockers, and bromocriptine.
In acromegalic patients, the most common side effects of octreotide acetate for injectable suspension include gallstones, diarrhea, abdominal pain, gas, flu-like symptoms, constipation, headache, low red blood cells, injection-site pain, gallstones, high blood pressure, dizziness and fatigue.
In carcinoid tumor and VIP-secreting tumor patients, the most common side effects of octreotide acetate for injectable suspension include back pain, fatigue, headache, abdominal pain, nausea, and dizziness.
These are not all of the possible side effects of octreotide acetate for injectable suspension. Call your doctor for medical advice about side effects. You are encouraged to report side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch or call 1-800-FDA-1088.
Octreotide acetate for injectable suspension is a prescription medication used in patients in whom initial treatment with octreotide acetate injection has been shown to be effective and tolerated for:
In patients with carcinoid tumors and VIP-secreting tumors, the effect of octreotide acetate injection and octreotide acetate for injectable suspension on tumor size, rate of growth and development of metastases, has not been determined.
Please see the full Prescribing Information.