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)
Cerebrovascular accident24.03.05.001; 17.08.01.0070.013155%
Congenital absence of bile ducts09.02.03.002; 03.19.01.001--Not Available
Cough22.02.03.001--
Death08.04.01.001--
Dermatitis23.03.04.002--Not Available
Diabetes mellitus14.06.01.001; 05.06.01.001--Not Available
Diarrhoea07.02.01.001--
Discomfort08.01.08.003--Not Available
Disorientation17.02.05.015; 19.13.01.0020.005262%Not Available
Disseminated intravascular coagulation24.01.01.010; 01.01.02.002--
Dizziness24.06.02.007; 17.02.05.003; 02.01.02.004--
Drug effect decreased08.06.01.008--Not Available
Drug ineffective08.06.01.006--Not Available
Dry mouth07.06.01.002--
Dyspepsia07.01.02.001--
Dysuria20.02.02.0020.007893%
Ecchymosis24.07.06.002; 23.06.01.001; 01.01.03.001--Not Available
Ejaculation disorder21.03.01.002--
Electrocardiogram abnormal13.14.05.001--Not Available
Erection increased21.03.01.004; 19.08.04.0020.010524%Not Available
Erythema23.03.06.0010.005262%Not Available
Exostosis15.02.04.0050.005262%
Feeling abnormal08.01.09.014--Not Available
Feeling hot08.01.09.009--Not Available
Feeling jittery08.01.09.016--Not Available
Fibrosis08.03.01.001--Not Available
Flushing24.03.01.002; 08.01.03.025; 23.06.05.003--
Fracture15.08.02.001; 12.04.02.001--
Fungal infection11.03.05.001--Not Available
Gastrooesophageal reflux disease07.02.02.003--
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