Sandostatin 50 mcg/ml Injection

Sandostatin 50 mcg/ml Injection Uses, Dosage, Side Effects, Food Interaction and all others data.

Trade Name Sandostatin 50 mcg/ml Injection
Generic Octreotide Acetate
Weight 50 mcg/ml
Type Injection
Therapeutic Class Growth hormone antagonist
Manufacturer Novartis (Bangladesh) Ltd.
Available Country Bangladesh
Last Updated: September 24, 2024 at 5:38 am
Sandostatin 50 mcg/ml Injection
Sandostatin 50 mcg/ml Injection

Uses

Acromegaly: Octreotide acetate injection is indicated to reduce blood levels of growth hormone and IGF-I (somatomedin C) in acromegaly patients who have had inadequate response to or cannot be treated with surgical resection, pituitary irradiation, and bromocriptine mesylate at maximally ... Read more

Dosage

Sandostatin 50 mcg/ml Injection dosage

Intramuscular-Acromegaly: Adult: Following initial control with SC therapy: As a depot preparation, initially 20 mg every 4 wk. Adjust if required after 3 mth to 10-30 mg every 4 wk. Max: 40 mg every 4 wk. Intravenous-Variceal haemorrhage in patients with cirrhosis: Adult: As continuous IV infusion: 25 mcg/hr for 48 hr (up to 5 days in patients at high risk of re-bleeding). Child: ≥1 mth: 1 mcg/kg/hr (up to 50 mcg/hr); given as continuous IV infusion. Higher doses may be needed initially, reduce dose gradually over 24 hr until bleeding has stopped. Subcutaneous-Prophylaxis of complications following pancreatic surgery: Adult: 100 mcg tid of a rapid-acting preparation given for 7 consecutive days, starting at least 1 hr before operation. Subcutaneous-Acromegaly: Adult: Initially 50 mcg tid, increased as necessary to usual dose 100-200 mcg tid. Max: 500 mcg tid. Subcutaneous-Secretory neoplasms: Adult: Initially, 50 mcg 1-2 times daily, increased gradually to up to 600 mcg daily in 2-4 divided doses according to response. Continued treatment is not recommended if there is no benefit within a wk of starting treatment for carcinoid tumour. Initial dose may be given via IV admin of a rapid response is required. Subcutaneous-HIV-associated diarrhoea: Adult: Initial dose 100 mcg tid. If symptoms are not controlled after 1 wk, increase dose to 250 mcg tid, if still not effective after 1 wk stop therapy.

Side Effects

Local pain, stinging, tingling at site of inj; anorexia, nausea, vomiting, abdominal pain, bloating, flatulence, loose stools, steatorrhoea; biliary tract abnormalities. Hypoglycaemia and hyperglycaemia, hypothyroidism, cardiac conduction abnormalitles, pancreatitis.

Precaution

Renal disease; risk of gall bladder disease; DM; hypothyroidism. Pregnancy, lactation, children, elderly. Monitor levels of vitamin B12 during long term therapy.

Interaction

Dosage adjustment of concurrent therapy may be necessary with calcium channel blockers, oral hypoglycaemics, β-blockers, diuretics. May increase concentration of bromocriptine.

Pregnancy & Breastfeeding use

Category B: Either animal-reproduction studies have not demonstrated a foetal risk but there are no controlled studies in pregnant women or animal-reproduction studies have shown an adverse effect (other than a decrease in fertility) that was not confirmed in controlled studies in women in the 1st trimester (and there is no evidence of a risk in later trimesters).

Contraindication

Hypersensitivity

Special Warning

Renal Impairment: Dosage may need to be reduced in severe renal impairment requiring dialysis.

Storage Condition

Store at 2-8° C. Stable at room temperature for up to 14 days.

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