 
 
What is Sandostatin® LAR® (octreotide acetate) used for?
SANDOSTATIN LAR is indicated for the treatment of:
- Patients with symptoms associated with functional gastro-entero-pancreatic endocrine tumours (e.g. carcinoid tumours with features of the carcinoid syndrome) or patients with advanced neuroendocrine tumours of the midgut or of unknown primary origin where non-midgut sites of origin have been excluded1 
- Patients with acromegaly in whom surgery is inappropriate or ineffective, or in the interim period until radiotherapy becomes fully effective1 
- Patients with TSH-secreting pituitary adenomas:1 - when secretion has not normalised after surgery and/or radiotherapy 
- in patients in whom surgery is inappropriate 
- in irradiated patients, until radiotherapy is effective. 
 
Resources for you:
 
  
						Reconstitution and preparation of SANDOSTATIN LAR
			
                            Reconstitution and preparation of SANDOSTATIN LAR
Reconstitution and preparation of SANDOSTATIN LAR
A guide on how to prepare and administer SANDOSTATIN LAR.
Resources for your patients:
 
  
						SASLAR - Home - patient guide - resource card
			
                            SASLAR - Home - patient guide - resource card
Your guide to SANDOSTATIN LAR
A guide to help you understand the treatment options you may be offered with SANDOSTATIN LAR.
Sandostatin LAR SmPC
TSH, thyroid-stimulating hormone.
Reference
- SANDOSTATIN® LAR® Summary of Product Characteristics. 
UK | February 2025 | FA-11214504
Adverse events should be reported. Reporting forms and information can be found at www.mhra.gov.uk/yellowcard. Adverse events should also be reported to Novartis online through the pharmacovigilance intake (PVI) tool at www.novartis.com/report, or alternatively email [email protected] or call 01276 698370.
 
              
      