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SANDOSTATIN 0.1 MG / 1ML INJECTION

 

 
 

 

GENERIC NAMES

MANUFACTURERS 

MEDICAL GROUP

MEDICAL ARTICLES

 

DRUGS IN :

 

 

FDA DRUGS

UNITED STATES

CANADA

UNITED KINGDOM

AUSTRALIA

GERMANY

FRANCE

MIDDLE EAST

KUWAIT

LEBANON

EGYPT

SYRIA

BAHRAIN

IRAN

JORDAN

SAUDI ARABIA

UNITED ARAB EMIRATES

 

 

 
 

SIZE:

0.1 MG / 1ML

 

GENERIC NAME:

OCTREOTIDE ACETATE

 

MANUFACTURER:

NOVARTIS PHARMA

 

UNIT:

 

ADMINISTRATION ROUTE:

 

FDA PREGNANCY GROUP:

B

 

INDICATIONS:

Vasoactive intestinal peptide tumor, adjunct

Acromegaly

Carcinoid tumor, adjunct

Diarrhea, carcinoid tumor

Diarrhea, vasoactive intestinal peptide tumor

 

SIDE EFFECTS:

Arrhythmias

bradycardia

Hyperglycemia

hypoglycemia

pancreatitis, acute

Gastrointestinal symptoms

pain, stinging, tingling, or burning sensation at injection site, with redness and swelling

Alopecia

dizziness or lightheadedness

edema

fatigue

fever

headache

redness or flushing of face

unusual weakness

 

ABSOLUTE CONTRAINDICATIONS :

 

RELATIVE CONTRAINDICATIONS :

>> Diabetes mellitus

>> Gallbladder disease or gallstones

Renal function impairment, severe

 

ADULT DOSE:

Gastrointestinal tumors- Subcutaneous, 50 mcg initially, administered two or three times a day, the dose being increased gradually according to patient tolerance and response. The following dosages are recommended for specific tumors: Carcinoid tumors- Initial: Subcutaneous, 100 to 600 mcg per day, administered in two to four divided doses, for the first two weeks of therapy. Maintenance: Subcutaneous, 50 to 1500 mcg per day. In clinical trials, the median maintenance dosage was 450 mcg per day. Vasoactive intestinal polypeptide-secreting tumors (VIPomas): Subcutaneous, 200 to 300 mcg per day, administered in two to four divided doses, for the first two weeks of therapy. Dosage may then be increased based on patient response. Acromegaly- Subcutaneous or intravenous, initially 50 mcg three times a day. Dosage is titrated every two weeks as needed, according to IGF-I concentrations, to a dose of 100 to 200 mcg three times a day; or, for rapid titration, dosage increase may be based on multiple serum growth hormone concentrations taken at one- to four-hour intervals over eight to twelve hours. Doses of up to 500 mcg three times a day have been used rarely. Note: Octreotide injection may be administered subcutaneously (the preferred route) or intravenously. To help prevent pain at the injection site, octreotide should be given in the smallest volume needed to achieve the proper dose. In emergencies, intravenous injections may be used cautiously. If an increase in dose fails to provide additional benefit, the dose should be reduced. [Complications of pancreatic surgery (prophylaxis of)]- Subcutaneous, 100 mcg three times a day for seven days beginning on the day of surgery at least one hour before laparatomy. [Bleeding gastroesophageal varices]- Intravenous infusion, 25 mcg per hour for forty-eight hours. Infusion should continue for up to five days in patients at high risk for rebleeding. [Pancreatic tumors] - Subcutaneous, 50 to 150 mcg initially, administered two times a day thirty minutes before meals, the dose being increased gradually according to patient tolerance and response. [Acquired immunodeficiency syndrome (AIDS)-associated diarrhea] - Subcutaneous, 100 to 1800 mcg per day.

 

MAXIMUM ADULT DOSE:

Acromegaly-1500 mcg daily.

 

PEDIATRIC DOSE:

Gastrointestinal tumors- Subcutaneous, 1 to 10 mcg per kg of body weight per day. 

 

MAXIMUM PEDIATRIC DOSE:

 

ELDERLY DOSE:

Gastrointestinal tumors- Subcutaneous, 50 mcg initially, administered two or three times a day, the dose being increased gradually according to patient tolerance and response. The following dosages are recommended for specific tumors: Carcinoid tumors- Initial: Subcutaneous, 100 to 600 mcg per day, administered in two to four divided doses, for the first two weeks of therapy. Maintenance: Subcutaneous, 50 to 1500 mcg per day. In clinical trials, the median maintenance dosage was 450 mcg per day. Vasoactive intestinal polypeptide-secreting tumors (VIPomas): Subcutaneous, 200 to 300 mcg per day, administered in two to four divided doses, for the first two weeks of therapy. Dosage may then be increased based on patient response. Acromegaly- Subcutaneous or intravenous, initially 50 mcg three times a day. Dosage is titrated every two weeks as needed, according to IGF-I concentrations, to a dose of 100 to 200 mcg three times a day; or, for rapid titration, dosage increase may be based on multiple serum growth hormone concentrations taken at one- to four-hour intervals over eight to twelve hours. Doses of up to 500 mcg three times a day have been used rarely. Note: Octreotide injection may be administered subcutaneously (the preferred route) or intravenously. To help prevent pain at the injection site, octreotide should be given in the smallest volume needed to achieve the proper dose. In emergencies, intravenous injections may be used cautiously. If an increase in dose fails to provide additional benefit, the dose should be reduced. [Complications of pancreatic surgery (prophylaxis of)]- Subcutaneous, 100 mcg three times a day for seven days beginning on the day of surgery at least one hour before laparatomy. [Bleeding gastroesophageal varices]- Intravenous infusion, 25 mcg per hour for forty-eight hours. Infusion should continue for up to five days in patients at high risk for rebleeding. [Pancreatic tumors] - Subcutaneous, 50 to 150 mcg initially, administered two times a day thirty minutes before meals, the dose being increased gradually according to patient tolerance and response. [Acquired immunodeficiency syndrome (AIDS)-associated diarrhea] - Subcutaneous, 100 to 1800 mcg per day.

 

 

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