Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Octreotide
Drug ID BADD_D02412
Description Acromegaly is a disorder caused by excess growth hormone (GH), increasing the growth of body tissues and causing metabolic dysfunction.[L14501] In most cases, it results from an anterior pituitary growth hormone-releasing tumor. Typically, the feet, hands, and face grow abnormally large; organomegaly and insulin resistance may also occur. Acromegaly is a life-threatening disease requiring life-long management.[L14501] Octreotide is a long-acting drug with pharmacologic activities that mimic those of the natural hormone, somatostatin, which inhibits the secretion of growth hormone.[L14513] Additionally, it is used for the treatment of acromegaly and symptoms arising from various tumors, including carcinoid tumors and vasoactive intestinal tumors (VIPomas).[L14513] In the past, octreotide has been administered solely by injection. On June 26, 2020, the first approved delayed-release oral somatostatin analog, Mycapssa, received FDA approval for the long term maintenance treatment of acromegaly. This drug was developed by Chiasma Inc.[L14495,L14507,L14528]
Indications and Usage For treatment of acromegaly and reduction of side effects from cancer chemotherapy
Marketing Status Not Available
ATC Code H01CB02
DrugBank ID DB00104
KEGG ID D00442
MeSH ID D015282
PubChem ID 448601
TTD Drug ID D02XIY
NDC Product Code 62147-0206; 35207-0002; 52416-118; 41524-0007; 52416-109; 69880-120
Synonyms Octreotide | SMS 201-995 | SMS 201 995 | SMS 201995 | SM 201-995 | SM 201 995 | SM 201995 | Sandoz 201-995 | Sandoz 201 995 | Sandoz 201995 | Compound 201-995 | Compound 201 995 | Compound 201995 | SAN 201-995 | SAN 201 995 | SAN 201995 | Octreotide Acetate | Octreotide Acetate Salt | Sandostatine | Sandostatin
Chemical Information
Molecular Formula C49H66N10O10S2
CAS Registry Number 79517-01-4
SMILES CC(C1C(=O)NC(CSSCC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)N1)CCCCN)CC2=CNC3=CC=CC=C32)CC4= CC=CC=C4)NC(=O)C(CC5=CC=CC=C5)N)C(=O)NC(CO)C(C)O)O
Chemical Structure
ADR Related Proteins Induced by Drug
ADR Term Protein Name UniProt AC TTD Target ID PMID
Not AvailableNot AvailableNot AvailableNot AvailableNot Available
ADRs Induced by Drug
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Blood glucose abnormal13.02.02.0080.003921%Not Available
Blood glucose decreased13.02.02.0010.007841%Not Available
Blood glucose increased13.02.02.0020.021563%Not Available
Blood growth hormone increased13.10.03.0100.007841%Not Available
Blood iron decreased13.11.01.0060.007841%Not Available
Blood potassium decreased13.11.01.0100.003921%Not Available
Blood potassium increased13.11.01.0110.003921%Not Available
Blood pressure decreased13.14.03.0020.039205%Not Available
Blood pressure diastolic decreased13.14.03.0030.041166%Not Available
Blood pressure diastolic increased13.14.03.0040.017642%Not Available
Blood pressure fluctuation24.06.01.0020.005881%Not Available
Blood pressure increased13.14.03.0050.164662%Not Available
Blood pressure systolic increased13.14.03.0060.115656%Not Available
Body temperature decreased13.15.01.0100.074490%Not Available
Body temperature increased13.15.01.0010.005881%Not Available
Bone disorder15.02.04.0040.003921%Not Available
Bone neoplasm16.29.01.001; 15.09.02.0010.003921%Not Available
Bone pain15.02.01.0010.011762%
Bradycardia02.03.02.0020.013722%Not Available
Breast cancer21.05.01.003; 16.10.01.0010.003921%Not Available
Breast mass21.05.04.0020.003921%Not Available
Bronchitis22.07.01.001; 11.01.09.0010.009801%
Bursitis15.04.01.0010.003921%Not Available
Carcinoid tumour16.24.04.002; 05.08.01.0020.003068%Not Available
Cardiac arrest02.03.04.0010.002045%
Cardiac failure02.05.01.001--
Cardiac failure congestive02.05.01.002--Not Available
Cardio-respiratory arrest02.03.04.002; 22.02.06.0070.001023%Not Available
Cerebrovascular accident24.03.05.001; 17.08.01.007--
Chest discomfort22.02.08.001; 08.01.08.019; 02.02.02.0090.011762%Not Available
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