Drug Interactions between Sandostatin LAR Depot and Signifor
This report displays the potential drug interactions for the following 2 drugs:
- Sandostatin LAR Depot (octreotide)
- Signifor (pasireotide)
Interactions between your drugs
No interactions were found between Sandostatin LAR Depot and Signifor. However, this does not necessarily mean no interactions exist. Always consult your healthcare provider.
Sandostatin LAR Depot
A total of 166 drugs are known to interact with Sandostatin LAR Depot.
- Sandostatin lar depot is in the drug class somatostatin and somatostatin analogs.
- Sandostatin lar depot is used to treat the following conditions:
Signifor
A total of 406 drugs are known to interact with Signifor.
- Signifor is in the drug class somatostatin and somatostatin analogs.
- Signifor is used to treat Cushing's Syndrome.
Drug and food/lifestyle interactions
octreotide food/lifestyle
Applies to: Sandostatin LAR Depot (octreotide)
MONITOR: Due to their gastrointestinal pharmacologic effects, somatostatin analogs (e.g., octreotide, lanreotide) may variously affect the absorption of dietary nutrients and concomitantly administered oral medications. Somatostatin analogs have been shown to prolong gastrointestinal transit time and inhibit intestinal absorption of some nutrients such as fat. Clinical data are limited, however. In case reports, octreotide has been reported to reduce the relative bioavailability of cyclosporine. Transplant rejection and significant reductions in cyclosporine levels, sometimes to undetectable levels, have been reported in association with the interaction. Vitamin K absorption was not affected when concomitantly administered with lanreotide according to the manufacturer.
MANAGEMENT: Clinicians should be aware of the potential for altered absorption of concomitantly administered oral medications during treatment with somatostatin analogs. Blood levels and clinical response should be monitored, particularly for drugs that have a narrow therapeutic index, and the dosages adjusted as necessary.
References (5)
- Landgraf R, Landgraf-Leurs MM, Nusser J, et al. (1987) "Effect of somatostatin analogue (SMS201-995) on cyclosporine levels." Transplantation, 44, p. 724-5
- Ho PJ, Boyajy LD, Greenstein E, Barkan AL (1993) "Effect of chronic octreotide treatment on intestinal absorption in patients with acromegaly." Dig Dis Sci, 38, p. 309-15
- Katz MD, Erstad BL (1989) "Octreotide, a new somatostatin analogue." Clin Pharm, 8, p. 255-73
- (2001) "Product Information. Sandostatin (octreotide)." Sandoz Pharmaceuticals Corporation
- (2007) "Product Information. Somatuline Depot (lanreotide)." Ipsen Inc
Therapeutic duplication warnings
Therapeutic duplication is the use of more than one medicine from the same drug category or therapeutic class to treat the same condition. This can be intentional in cases where drugs with similar actions are used together for demonstrated therapeutic benefit. It can also be unintentional in cases where a patient has been treated by more than one doctor, or had prescriptions filled at more than one pharmacy, and can have potentially adverse consequences.
Growth hormone release inhibitors
Therapeutic duplication
The recommended maximum number of medicines in the 'growth hormone release inhibitors' category to be taken concurrently is usually one. Your list includes two medicines belonging to the 'growth hormone release inhibitors' category:
- Sandostatin LAR Depot (octreotide)
- Signifor (pasireotide)
Note: In certain circumstances, the benefits of taking this combination of drugs may outweigh any risks. Always consult your healthcare provider before making changes to your medications or dosage.
See also
Drug Interaction Classification
Highly clinically significant. Avoid combinations; the risk of the interaction outweighs the benefit. | |
Moderately clinically significant. Usually avoid combinations; use it only under special circumstances. | |
Minimally clinically significant. Minimize risk; assess risk and consider an alternative drug, take steps to circumvent the interaction risk and/or institute a monitoring plan. | |
No interaction information available. |
Further information
Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.
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