Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Levodopa
Drug ID BADD_D02439
Description Levodopa is a prodrug of dopamine that is administered to patients with Parkinson's due to its ability to cross the blood-brain barrier[Label]. Levodopa can be metabolised to dopamine on either side of the blood-brain barrier and so it is generally administered with a dopa decarboxylase inhibitor like carbidopa to prevent metabolism until after it has crossed the blood-brain barrier[Label,A177781]. Once past the blood-brain barrier, levodopa is metabolized to dopamine and supplements the low endogenous levels of dopamine to treat symptoms of Parkinson's[Label]. The first developed drug product that was approved by the FDA was a levodopa and carbidopa combined product called Sinemet that was approved on May 2, 1975[A177781,L6133].
Indications and Usage For the treatment of idiopathic Parkinson's disease (Paralysis Agitans), postencephalitic parkinsonism, symptomatic parkinsonism which may follow injury to the nervous system by carbon monoxide intoxication, and manganese intoxication.
Marketing Status Not Available
ATC Code N04BA01
DrugBank ID DB01235
KEGG ID D00059
MeSH ID D007980
PubChem ID 6047
TTD Drug ID D08HVR
NDC Product Code 51846-1052; 51552-1348; 10144-342; 51846-1053; 65977-0126; 62331-013; 49452-2680; 11014-0443; 70600-019; 51927-0049; 64220-199; 58624-0238; 17333-059; 58624-0234
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 C9H11NO4
CAS Registry Number 59-92-7
SMILES C1=CC(=C(C=C1CC(C(=O)O)N)O)O
Chemical Structure
ADR Related Proteins Induced by Drug
ADR Term Protein Name UniProt AC TTD Target ID PMID
Adverse drug reactionProtein c-FosP01100T28025Not Available
Dyskinesias and movement disorders NECE3 ubiquitin-protein ligase parkinO60260Not AvailableNot Available
Parkinson's diseaseOpioid growth factor receptorQ9NZT2T13741Not Available
Toxicity to various agentsCatechol O-methyltransferaseP21964T76904Not Available
ADRs Induced by Drug
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Abnormal dreams19.02.03.001; 17.15.02.0010.001657%Not Available
Anhedonia19.15.02.0070.001657%Not Available
Anxiety19.06.02.0020.004143%
Apathy19.04.04.0020.001657%Not Available
Aphasia19.21.01.001; 17.02.03.0010.001657%
Arthralgia15.01.02.0010.002486%
Asthenia08.01.01.0010.005800%Not Available
Cerebral haemorrhage24.07.04.001; 17.08.01.0030.001657%Not Available
Chest pain22.02.08.003; 08.01.08.002; 02.02.02.0110.001657%Not Available
Choking22.02.05.0010.002486%Not Available
Confusional state19.13.01.001; 17.02.03.0050.001657%
Cough22.02.03.0010.020715%
Death08.04.01.001--
Delirium19.13.02.0010.001297%
Dementia19.20.02.001; 17.03.01.0010.001657%Not Available
Depression19.15.01.0010.004143%
Disorientation19.13.01.002; 17.02.05.0150.001657%Not Available
Disturbance in attention19.21.02.002; 17.03.03.0010.000648%
Dizziness02.01.02.004; 24.06.02.007; 17.02.05.0030.002486%
Drug dependence19.07.02.0090.001657%Not Available
Drug withdrawal syndrome19.07.02.011; 08.06.02.0040.001657%Not Available
Dysgeusia17.02.07.003; 07.14.03.0010.001657%
Dyskinesia17.01.02.0060.010772%
Dysphoria19.04.02.0040.001657%Not Available
Dyspnoea22.02.01.004; 02.01.03.002--
Dystonia17.01.03.0010.001657%Not Available
Eczema23.03.04.0060.001657%
Fatigue08.01.01.0020.004143%
Fibroma16.02.02.010; 15.09.01.0040.002486%Not Available
Gait disturbance08.01.02.002; 17.02.05.0160.001657%
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