Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Pimavanserin
Drug ID BADD_D02451
Description Psychotic symptoms associated with Parkinson's disease (PD) are relatively common, reducing quality of life and prognosis for individuals with PD.[A232783] Pimavanserin (ACP-103), marketed under the trade name Nuplazid, is a drug developed by Acadia Pharmaceuticals for the treatment of psychosis related to Parkinson's disease. Due to its actions at serotonin receptors and lack of effects on dopamine receptors, pimavanserin treats hallucinations and delusions without causing extrapyramidal symptoms.[A232613] It was initially approved by the FDA in 2016 and is now under review as a potential treatment for dementia related psychosis. As of April 2021, FDA approval has not been granted for this indication, despite previous breakthrough designation.[L32913]
Indications and Usage Investigated for use/treatment in neurologic disorders, parkinson's disease, psychosis, schizophrenia and schizoaffective disorders, and sleep disorders.
Marketing Status Not Available
ATC Code N05AX17
DrugBank ID DB05316
KEGG ID D08969
MeSH ID C510793
PubChem ID 10071196
TTD Drug ID D0J8JP
NDC Product Code Not Available
Synonyms pimavanserin | N-(4-fluorophenylmethyl)-N-(1-methylpiperidin-4-yl)-N'-(4-(2-methylpropyloxy)phenylmethyl)carbamide | ACP 103 | ACP103 | ACP-103 | Nuplazid | pimavanserin tartrate | urea, n-((4-fluorophenyl)methyl)-n-(1-methyl-4-piperidinyl)-n'-((4-(2-methylpropoxy)phenyl)methyl)-, (2R,3R)-2,3-dihydroxybutanedioate (2:1) | bis(1-(4-fluorobenzyl)-1-(1-methylpiperidin-4-yl)-3-(4-(2-methylpropoxy)benzyl)urea) (2R,3R)-2,3-dihydroxybutanedioate
Chemical Information
Molecular Formula C25H34FN3O2
CAS Registry Number 706779-91-1
SMILES CC(C)COC1=CC=C(C=C1)CNC(=O)N(CC2=CC=C(C=C2)F)C3CCN(CC3)C
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)
Throat irritation22.02.05.013; 07.05.03.004--Not Available
Throat tightness22.02.05.015; 19.01.02.0050.003010%Not Available
Thrombosis24.01.01.006--Not Available
Tongue disorder07.14.01.0020.000602%Not Available
Transient ischaemic attack17.08.04.001; 24.04.06.005--
Tremor17.01.06.0020.018662%
Unresponsive to stimuli17.02.05.0310.006923%Not Available
Urinary incontinence17.05.01.008; 20.02.02.0100.001806%
Urinary retention20.02.02.011--
Urinary tract infection20.08.02.001; 11.01.14.0040.021371%
Urticaria23.04.02.001; 10.01.06.001--
Vertigo17.02.12.002; 04.04.01.003--
Vision blurred06.02.06.007; 17.17.01.010--
Visual impairment06.02.06.008--Not Available
Vomiting07.01.07.003--
Weight decreased13.15.01.005--
Weight increased13.15.01.006--
Wheezing22.03.01.009--
Withdrawal syndrome19.07.02.005; 08.06.02.012--Not Available
Wrist fracture15.08.03.007; 12.04.01.0080.000602%
Mental status changes19.07.01.001--Not Available
Mobility decreased17.02.05.018; 15.03.01.003; 08.01.03.0300.003612%Not Available
Hypervigilance19.01.02.0060.000903%Not Available
Musculoskeletal disorder15.03.01.0040.000602%Not Available
Seasonal allergy10.01.04.001; 06.04.01.013; 22.04.04.0080.000602%Not Available
Peripheral swelling08.01.03.053; 02.05.04.0150.037023%Not Available
Emotional distress19.04.02.008--Not Available
Abasia17.02.05.035; 08.01.02.0070.014448%Not Available
Balance disorder17.02.02.0070.014147%Not Available
Cervical vertebral fracture12.04.04.003; 15.08.05.0020.000236%Not Available
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