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)
Dizziness24.06.02.007; 17.02.05.003; 02.01.02.0040.056848%
Dizziness postural24.06.02.008; 17.02.05.004; 02.01.02.0050.005881%Not Available
Drug dependence19.07.02.0090.003921%Not Available
Dry skin23.03.03.0010.003921%
Dyspepsia07.01.02.0010.015682%
Dysphagia07.01.06.003--
Dyspnoea22.02.01.004; 02.01.03.0020.084292%
Dyspnoea exertional22.02.01.005; 02.01.03.0030.007841%Not Available
Dysuria20.02.02.0020.007841%
Eating disorder19.09.01.008; 14.03.01.0080.021563%Not Available
Erythema23.03.06.0010.025483%Not Available
Eye disorder06.08.03.0010.003921%Not Available
Eye irritation06.04.05.0030.003921%Not Available
Eye pain06.08.03.0020.003921%
Eye swelling06.08.03.0030.003921%Not Available
Eyelid ptosis17.17.02.004; 06.05.01.0020.003921%Not Available
Faeces discoloured07.01.03.0020.015682%Not Available
Fatigue08.01.01.0020.109775%
Fear19.06.03.0010.003921%Not Available
Feeling abnormal08.01.09.0140.047046%Not Available
Feeling hot08.01.09.0090.013722%Not Available
Flank pain20.02.03.006; 15.03.04.003; 08.01.08.0070.003921%
Flatulence07.01.04.0020.023523%
Fluid retention20.01.02.003; 14.05.06.0020.005881%Not Available
Flushing23.06.05.003; 08.01.03.025; 24.03.01.0020.049007%
Frequent bowel movements07.02.04.0020.011762%Not Available
Gait disturbance17.02.05.016; 08.01.02.0020.023523%
Gallbladder disorder09.03.02.0010.007841%Not Available
Gastrooesophageal reflux disease07.02.02.0030.005881%
Gastrointestinal disorder07.11.01.0010.009801%Not Available
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