Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Treprostinil
Drug ID BADD_D02268
Description Treprostinil is a synthetic analogue of prostacyclin, used to treat pulmonary hypertension.
Indications and Usage For use as a continuous subcutaneous infusion or intravenous infusion (for those not able to tolerate a subcutaneous infusion) for the treatment of pulmonary arterial hypertension in patients with NYHA Class II-IV symptoms to diminish symptoms associated with exercise.
Marketing Status approved; investigational
ATC Code B01AC21
DrugBank ID DB00374
KEGG ID D06213
MeSH ID C427248
PubChem ID 6918140
TTD Drug ID D01WUA
NDC Product Code 0703-0696; 0781-3430; 11014-0094; 66302-350; 66302-648; 66302-748; 66302-361; 66302-363; 66302-620; 66302-720; 0703-0676; 43598-646; 43598-647; 66302-302; 66302-325; 66302-616; 66302-362; 0703-0666; 14501-0015; 42023-209; 62332-515; 66302-110; 66302-300; 66302-610; 54893-0024; 43598-649; 62332-514; 62332-517; 66302-102; 66302-206; 66302-732; 58159-041; 68245-0008; 43598-648; 66302-120; 66302-600; 66302-650; 66302-764; 0703-0686; 0781-3420; 0781-3425; 81861-0029; 66302-101; 66302-310; 66302-630; 66302-664; 0781-3427; 42023-206; 66302-105; 66302-640; 42023-207; 62332-516; 66302-632; 66302-716; 42023-208
UNII RUM6K67ESG
Synonyms treprostinil | ((1R,2R,3AS,9AS)-2-hydroxy-1-((3S)-3-hydroxyoctyl)-2,3,3A,4,9,9A-hexahydro-1H-cylopent(b)naphthalen-5-yl)oxy)acetate | treprostinil sodium | trepostinil sodium | Orenitram | UT-15 | UT-15C | Remodulin | treprostinil diolamine | treprostinil diolamin | treprostinil diethanolamine
Chemical Information
Molecular Formula C23H34O5
CAS Registry Number 81846-19-7
SMILES CCCCCC(CCC1C(CC2C1CC3=C(C2)C(=CC=C3)OCC(=O)O)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)
Injection site reaction08.02.03.014; 12.07.03.0150.000403%
Injection site vesicles12.07.03.051; 08.02.03.051; 23.03.01.0240.000280%Not Available
Insomnia19.02.01.002; 17.15.03.002--
Interstitial lung disease22.01.02.003; 10.02.01.0330.000781%Not Available
Intestinal obstruction07.13.01.0020.000411%Not Available
Intussusception07.13.01.0080.000082%Not Available
Joint effusion15.01.02.0050.000082%
Joint swelling15.01.02.0040.001768%Not Available
Laryngeal pain22.12.03.010--
Left ventricular failure02.05.02.0010.000123%Not Available
Lethargy08.01.01.008; 19.04.04.004; 17.02.04.0030.002311%
Listless19.04.04.003; 08.01.01.0120.000123%Not Available
Liver disorder09.01.08.001--Not Available
Loss of consciousness17.02.04.0040.002558%Not Available
Lung disorder22.02.07.0010.000592%Not Available
Lymphoedema24.09.01.001; 01.09.01.0060.000082%
Malabsorption14.02.01.004; 07.17.01.0010.000082%
Malaise08.01.01.0030.014006%
Mass08.03.05.003--Not Available
Melaena24.07.02.013; 07.12.02.004--Not Available
Menstruation delayed21.01.02.003; 05.05.01.0100.000280%Not Available
Micturition urgency20.02.02.0060.000181%
Migraine24.03.05.003; 17.14.02.0010.004005%Not Available
Muscle spasms15.05.03.004--
Musculoskeletal pain15.03.04.0070.001563%
Myalgia15.05.02.0010.004507%
Nasal congestion22.04.04.0010.003084%
Nausea07.01.07.0010.039486%
Neck pain15.03.04.0090.001406%
Nervousness19.06.02.0030.001365%Not Available
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ADReCS-Target
Drug Name ADR Term Target
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