Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Leuprolide acetate
Drug ID BADD_D01260
Description Leuprolide is a synthetic 9-residue peptide analogue of gonadotropin-releasing hormone (GnRH). Unlike the endogenous decapeptide GnRH, leuprolide contains a single D-amino acid (D-leucyl) residue, which helps to increase its circulating half-life from three to four minutes to approximately three hours.[A203222] As a GnRH mimic, leuprolide is capable of binding to the GnRH receptor (GnRHR) and inducing downstream modulation of both gonadotropin hormone and sex steroid levels. Prolonged activation of GnRHR results in significant downregulation of sex steroid levels, which is primarily responsible for the clinical efficacy of leuprolide in diverse conditions, including advanced prostate cancer, endometriosis, and central precocious puberty.[A203126, A203132] Leuprolide was first approved in 1985 as a daily subcutaneous injection under the tradename Lupron™ by Abbvie Endocrine Inc.[L13850] Since this initial approval, various long-acting intramuscular and subcutaneous products have been developed such that patients can be dosed once every six months.[L13781, L13790] Leuprolide remains frontline therapy in all conditions for which it is indicated for use.
Indications and Usage Leuprolide is indicated for the palliative treatment of advanced prostate cancer[L13781, L13790] as well as for the treatment of pediatric patients with central precocious puberty (CPP).[L13784, L13787] Leuprolide mesylate, as an injectable emulsion, is indicated for the treatment of adult patients with advanced prostate cancer.[L34415] In combination with oral [norethisterone] (also known as norethindrone), leuprolide is also indicated for the initial treatment of the symptoms of endometriosis.[L10310] Finally, in combination with iron supplementation, leuprolide is indicated for the preoperative hematological improvement of anemic patients with uterine leiomyomata (uterine fibroids).[L13814]
Marketing Status approved; investigational
ATC Code L02AE02
DrugBank ID DB00007
KEGG ID D00989
MeSH ID D016729
PubChem ID 657180
TTD Drug ID D04ASH
NDC Product Code 0781-4003; 11532-1450; 11532-1456; 41701-013; 51927-0126; 0074-2108; 0074-2440; 0074-3473; 0074-3683; 47335-936; 62935-453; 11532-3338; 59651-089; 62935-163; 72664-611; 11532-1451; 11532-3680; 55150-478; 69097-909; 11532-1454; 11532-3662; 54127-9002; 71052-620; 0074-2282; 62935-753; 11532-1455; 59149-002; 0074-3642; 0074-3663; 0074-3779; 51927-0303; 0074-3575; 0074-3641; 62935-461; 11532-1457; 0074-3346; 11532-1452; 38779-2629; 62935-223; 62935-303; 70121-2537; 11532-1453; 60870-0425; 16714-572; 62935-153; 63629-8821; 0074-9694
UNII 37JNS02E7V
Synonyms Leuprolide | Leuprorelin | Enantone | Leuprolide Acetate | Acetate, Leuprolide | Leuprolide Monoacetate | Monoacetate, Leuprolide | Leuprolide, (L-Leu)-Isomer | Lupron | TAP-144 | TAP 144 | TAP144 | A-43818 | A 43818 | A43818 | Leuprolide, (DL-Leu)-Isomer
Chemical Information
Molecular Formula C61H88N16O14
CAS Registry Number 74381-53-6
SMILES CCNC(=O)C1CCCN1C(=O)C(CCCN=C(N)N)NC(=O)C(CC(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC2=CC=C( C=C2)O)NC(=O)C(CO)NC(=O)C(CC3=CNC4=CC=CC=C43)NC(=O)C(CC5=CN=CN5)NC(=O)C6CCC(=O)N 6.CC(=O)O
Chemical Structure
ADRs Induced by Drug
*The priority for ADR severity classification is based on FAERS assessment, followed by the most severe level in CTCAE rating. If neither is available, it will be displayed as 'Not available'.
**The 'Not Available' level is hidden by default and can be restored by clicking on the legend twice..
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Intervertebral disc protrusion15.10.01.0040.002151%Not Available
Contusion15.03.05.007; 24.07.06.001; 23.03.11.002; 12.01.06.001--
Musculoskeletal chest pain22.09.01.001; 15.03.04.0120.002151%
Fluid imbalance14.05.01.003--Not Available
Central nervous system lesion17.02.10.011--Not Available
Exercise tolerance decreased08.01.03.0360.002151%Not Available
Prostatomegaly21.04.01.0020.001434%Not Available
Large intestine polyp16.05.02.006; 07.20.01.010--Not Available
Acute coronary syndrome24.04.04.011; 02.02.02.0150.001434%Not Available
Sticky skin23.03.03.019--Not Available
Respiratory tract congestion22.02.07.003--Not Available
Musculoskeletal stiffness15.03.05.027--Not Available
Musculoskeletal discomfort15.03.04.0010.005593%Not Available
Injection site swelling12.07.03.018; 08.02.03.0170.034560%Not Available
Growth retardation05.03.02.007; 15.03.05.016; 14.03.02.031--
Nodule08.03.05.002--Not Available
Affect lability19.04.01.0010.009465%Not Available
Injection site discomfort08.02.03.018; 12.07.03.0190.028250%Not Available
Haemorrhage24.07.01.002--Not Available
Haemorrhage urinary tract24.07.01.007; 20.02.03.0050.002151%Not Available
Adenomyosis21.07.01.0110.002151%Not Available
Pulmonary mass22.02.07.0040.005736%Not Available
Weight abnormal13.15.01.016--Not Available
Hypoaesthesia oral17.02.06.021; 07.05.05.0030.004876%Not Available
Cognitive disorder17.03.03.003; 19.21.02.0010.023518%
Male sexual dysfunction21.03.02.012; 19.08.05.0030.003155%Not Available
Major depression19.15.01.0030.002151%Not Available
Injection site nodule23.07.04.009; 12.07.03.034; 08.02.03.0340.050621%Not Available
Cancer pain16.32.03.0040.004302%Not Available
Precocious puberty21.03.02.009; 05.05.03.001--
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