Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Lanreotide
Drug ID BADD_D02461
Description Lanreotide is a drug employed in the management of acromegaly (a hormonal condition caused by excess growth hormone) in addition to symptoms caused by neuroendocrine tumors, especially carcinoid syndrome. This drug is a long-acting analog of the drug somatostatin, a growth hormone inhibitor. Lanreotide is manufactured by the company, _Ipsen Pharmaceuticals_ as lanreotide acetate, and marketed as _Somatuline_. It is approved in several countries worldwide, including the United Kingdom, Australia, and Canada. Lanreotide was first approved for use in the United States by the FDA on August 30, 2007.
Indications and Usage Lanreotide is a somatostatin analog approved for treatment of neuroendocrine tumours and acromegaly. (2)
Marketing Status Not Available
ATC Code H01CB03
DrugBank ID DB06791
KEGG ID D04666
MeSH ID C060347
PubChem ID 6918011
TTD Drug ID D0M2YE
NDC Product Code 52416-117
Synonyms lanreotide | 3-(2-naphthyl)alanyl-cystinyl-tyrosyl-tryptophyl-lysyl-valyl-cystinyl-threonine amide | D-Nal-Cys-Tyr-Trp-Lys-Val-Cys-Thr-NH2 | angiopeptin | naphthalenyl-cyclo(cysteinyl-tyrosyl-tryptophyl-lysyl-valyl-cysteinyl)threoninamide | L-Threoninamide, 3-(2-naphthalenyl)-D-alanyl-L-cysteinyl-L-tyrosyl-D-tryptophyl-L-lysyl-L-valyl-L-cysteinyl-, cyclic (2-7)-disulfide | Nal-cyclo(Cys-Tyr-Trp-Lys-Val-Cys)-Thr-NH2 | Nal-cyclo(Cys-Tyr-Trp-Lys-Val-Cys)Thr-NH2 | 2-naphthylalanyl-cyclo(cysteinyl-tyrosyl-tryptophyl-lysyl-valyl-cysteinyl)-threoninamide | 3-(2-naphthyl)-D-Ala-Cys-Tyr-D-Trp-Lys-Val-Cys-Thr-NH2 | naphthyl-cyclo(Cys-Tyr-Trp-Lys-Val-Cys)Thr-NH2 | BIM 23014 | BIM-23014 | DC 13-116 | DC13-116 | DC-13-116 | lanreotide acetate | Somatulina | Somatuline | lanreotide-SR | BIM 23014 C | BIM 23014C | BIM-23014 C | 188Re-lanreotide | Somatulin
Chemical Information
Molecular Formula C54H69N11O10S2
CAS Registry Number 108736-35-2
SMILES CC(C)C1C(=O)NC(CSSCC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)N1)CCCCN)CC2=CNC3=CC=CC=C32)CC 4=CC=C(C=C4)O)NC(=O)C(CC5=CC6=CC=CC=C6C=C5)N)C(=O)NC(C(C)O)C(=O)N
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)
Abdominal discomfort07.01.06.0010.021563%Not Available
Abdominal distension07.01.04.0010.021563%
Abdominal pain07.01.05.0020.031364%
Abdominal pain upper07.01.05.0030.039205%
Acute respiratory failure22.02.06.001; 14.01.04.0040.001023%Not Available
Alopecia23.02.02.0010.027444%
Anxiety19.06.02.0020.015682%
Arthralgia15.01.02.0010.021563%
Arthritis15.01.01.0010.003921%
Asthenia08.01.01.0010.025483%Not Available
Back pain15.03.04.0050.013722%
Blood glucose decreased13.02.02.0010.005881%Not Available
Blood glucose increased13.02.02.0020.017642%Not Available
Blood growth hormone increased13.10.03.0100.005881%Not Available
Blood pressure increased13.14.03.0050.007841%Not Available
Bone pain15.02.01.0010.003921%
Breast cancer21.05.01.003; 16.10.01.0010.003921%Not Available
Cardiac failure02.05.01.0010.001023%
Chest discomfort08.01.08.019; 02.02.02.009; 22.02.08.0010.005881%Not Available
Chest pain22.02.08.003; 08.01.08.002; 02.02.02.0110.007841%Not Available
Cholelithiasis09.03.01.0020.009801%Not Available
Cold sweat23.02.03.002; 08.01.03.0240.003921%Not Available
Confusional state19.13.01.001; 17.02.03.005--
Constipation07.02.02.001--
Crying12.02.11.001; 08.01.03.005; 19.04.02.002; 17.02.05.0130.003921%Not Available
Death08.04.01.0010.016875%
Defaecation urgency07.02.04.0010.003921%Not Available
Dehydration14.05.05.001--
Depression19.15.01.0010.009801%
Diarrhoea07.02.01.0010.156821%
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