Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Levodopa-4'-monophosphate
Drug ID BADD_D01274
Description Foslevodopa is under investigation in clinical trial NCT04750226 (Study to Assess Adverse Events and Change in Disease Activity of 24-hour Continuous Subcutaneous Infusion of ABBV-951 in Adult Participants With Advanced Parkinson's Disease).
Indications and Usage Not Available
Marketing Status investigational
ATC Code N04BA01
DrugBank ID DB16683
KEGG ID D00059
MeSH ID D007980
PubChem ID 127766
TTD Drug ID DP7GK8
NDC Product Code 62526-1912
UNII 37NQZ0J76I
Synonyms Levodopa | L-Dopa | L Dopa | 3-Hydroxy-L-tyrosine | 3 Hydroxy L tyrosine | L-3,4-Dihydroxyphenylalanine | L 3,4 Dihydroxyphenylalanine | Levopa | Larodopa | Dopaflex | Dopar
Chemical Information
Molecular Formula C9H12NO7P
CAS Registry Number 97321-87-4
SMILES C1=CC(=C(C=C1CC(C(=O)O)N)O)OP(=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)
Abdominal pain07.01.05.002--
Arthralgia15.01.02.001--
Asthenia08.01.01.001---
Back pain15.03.04.005--
Blood uric acid increased13.02.04.001---
Constipation07.02.02.001--
Diarrhoea07.02.01.001--
Dizziness02.11.04.006; 17.02.05.003; 24.06.02.007--
Dysgeusia07.14.03.001; 17.02.07.003--
Dyspepsia07.01.02.001--
Fatigue08.01.01.002--
Gastrointestinal disorder07.11.01.001---
Gastrointestinal pain07.01.05.005--
Gout14.09.01.001; 15.01.06.001---
Headache17.14.01.001--
Hypercalcaemia05.04.01.002; 14.04.01.003--
Hypercalciuria05.04.01.003; 14.04.01.006; 20.02.01.007---
Hyperuricaemia14.09.01.003--
Infection11.01.08.002---
Influenza11.05.03.001; 22.07.02.001---
Injection site erythema08.02.03.001; 12.07.03.001; 23.03.06.015---
Injection site irritation08.02.03.027; 12.07.03.027---
Muscle spasms15.05.03.004--
Nausea07.01.07.001--
Nephrolithiasis20.04.01.002--
Nervous system disorder17.02.10.001---
Pain in extremity15.03.04.010--
Palpitations02.11.04.012--
Parosmia17.04.04.002; 22.04.03.007---
Urethral disorder20.07.01.002---
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