Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Alprostadil
Drug ID BADD_D00086
Description Alprostadil is produced endogenously and causes vasodilation by means of a direct effect on vascular and ductus arteriosus (DA) smooth muscle, preventing or reversing the functional closure of the DA that occurs shortly after birth. This results in increased pulmonary or systemic blood flow in infants. In infants, it is used for palliative, not definitive, therapy to temporarily maintain the patency of the ductus arteriosus until corrective or palliative surgery can be performed in neonates who have congenital heart defects and who depend upon the patent ductus for survival. In adults, it is used for the treatment of erectile dysfunction due to neurogenic, vasculogenic, psychogenic, or mixed etiology.
Indications and Usage For palliative, not definitive, therapy to temporarily maintain the patency of the ductus arteriosus until corrective or palliative surgery can be performed in neonates who have congenital heart defects and who depend upon the patent ductus for survival. Also for the treatment of erectile dysfunction due to neurogenic, vasculogenic, psychogenic, or mixed etiology.
Marketing Status Prescription; Discontinued
ATC Code C01EA01; G04BE01
DrugBank ID DB00770
KEGG ID D00180
MeSH ID D000527
PubChem ID 5280723
TTD Drug ID D0I4DQ
NDC Product Code 0037-8130; 63190-0600; 40016-010; 0009-7686; 38779-0944; 0009-3701; 52244-020; 0703-1501; 0037-8110; 82231-101; 0009-5181; 71052-146; 52244-010; 49452-0073; 63539-121; 0009-0042; 0037-8120; 52244-040; 0009-3169; 0037-8140; 68245-0007; 63902-100; 0009-5182; 45542-1152; 65035-101; 51552-0498; 63539-221; 61556-010; 51927-2196
Synonyms Alprostadil | PGE1alpha | Prostaglandin E1alpha | PGE1 | Lipo-PGE1 | Lipo PGE1 | Prostaglandin E1 | Caverject | Edex | Prostavasin | Muse | Viridal | Vasaprostan | Minprog | Sugiran | Prostin VR | Prostine VR
Chemical Information
Molecular Formula C20H34O5
CAS Registry Number 745-65-3
SMILES CCCCCC(C=CC1C(CC(=O)C1CCCCCCC(=O)O)O)O
Chemical Structure
ADR Related Proteins Induced by Drug
ADR Term Protein Name UniProt AC TTD Target ID PMID
MiosisVasopressin V1a receptorP37288T792323460310; 6385626; 3485638; 716972
ADRs Induced by Drug
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Haematoma24.07.01.001--
Haematuria24.07.01.047; 20.02.01.006--
Haemoglobin13.01.05.018--Not Available
Haemorrhage intracranial24.07.04.003; 17.08.01.008--
Hair growth abnormal23.02.06.0060.007893%Not Available
Headache17.14.01.001--
Hyperaemia24.03.02.002--Not Available
Hyperbilirubinaemia14.11.01.010; 09.01.01.003; 01.06.04.003--Not Available
Hypercapnia22.02.02.002; 14.01.04.001--Not Available
Hypercholesterolaemia14.08.01.001--Not Available
Hyperglycaemia14.06.02.002; 05.06.02.002--
Hyperhidrosis23.02.03.004; 08.01.03.0280.005262%
Hyperkalaemia14.05.03.001--
Hypertension24.08.02.001--
Hypertriglyceridaemia14.08.02.001--
Hypertrophic osteoarthropathy22.02.08.014; 16.32.01.004; 15.02.04.022--Not Available
Hypertrophy08.03.04.005--Not Available
Hypoaesthesia17.02.06.023--Not Available
Hypochromic anaemia01.03.02.004--Not Available
Hypoglycaemia14.06.03.001; 05.06.03.001--
Hypokalaemia14.05.03.0020.036834%
Hypotension24.06.03.0020.031572%
Hypothermia12.05.03.001; 08.05.01.003--
Infection11.01.08.002--Not Available
Influenza22.07.02.001; 11.05.03.001--Not Available
Influenza like illness08.01.03.010--
Inguinal hernia07.16.02.001--Not Available
Injection site bruising24.07.06.017; 23.03.11.015; 12.07.03.042; 08.02.03.042--Not Available
Injection site haematoma24.07.01.009; 12.07.03.004; 08.02.03.004--Not Available
Injection site haemorrhage24.07.01.010; 12.07.03.005; 08.02.03.005--Not Available
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