Species

KNApSAcK Entry

Organism name Physostigma venenosum
Genus Physostigma
Family Fabaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Physostigma venenosum
Linked NCBI taxonomy ID 271807
Linked level species

Family

Family in NCBI taxonomy Fabaceae
ID 3803

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class rosids
ID 71275

Natural Activity

List (18)

Species Activity
Physostigma venenosum Balf. Anticholinesterase
Physostigma venenosum Balf. Anticuraroid
Physostigma venenosum Balf. Antidote
Physostigma venenosum Balf. Antidote, curare
Physostigma venenosum Balf. Cardiodepressant
Physostigma venenosum Balf. Insecticide
Physostigma venenosum Balf. Mitotic
Physostigma venenosum Balf. Myotic
Physostigma venenosum Balf. Negative Chronotropic
Physostigma venenosum Balf. Paralytic
Physostigma venenosum Balf. Parasiticide
Physostigma venenosum Balf. Parasympathomimetic
Physostigma venenosum Balf. Pediculicide
Physostigma venenosum Balf. Peristaltic
Physostigma venenosum Balf. Poison
Physostigma venenosum Balf. Rodenticide
Physostigma venenosum Balf. Sedative
Physostigma venenosum Balf. Spasmogenic

Metabolite list (5)

KNApSAcK ID name ChEMBL link CTD link # of proteins in
ChEMBL interaction
/ related OMIM
/ related KEGG DISEASE
# of genes in
CTD interaction
/ related diseases
KCF-S
cluster
phytochemical
cluster
figure
C00003674 External link 512 Stigmasterol
/ beta-Stigmasterol
CHEMBL66943
CHEMBL186373
CHEMBL400247
CHEMBL1568947
D013265
5 / 0 / 0 1 / 0 No. 53 No. 11
C00001757 External link 512 Physostigmine
CHEMBL94
CHEMBL11773
CHEMBL306319
CHEMBL76640
CHEMBL382351
CHEMBL1243269
D010830
109 / 58 / 52 5 / 83 No. 2568 No. 4
C00001726 External link 512 Eseridine
CHEMBL123248
C060406
2 / 1 / 0 No. 2568 No. 4
C00001758 External link 512 Physovenine
CHEMBL362444
CHEMBL205940
CHEMBL205231
C092643
2 / 1 / 0 No. 2568 No. 4
C00001725 External link 512 Eseramine
CHEMBL77799
No. 2568 No. 4

Human Protein / Gene in interactions

114 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P06276 Cholinesterase Hydrolase C00001726 C00001757 C00001758 0 / 0
P22303 Acetylcholinesterase Hydrolase C00001726 C00001757 C00001758 1 / 0
P09884 DNA polymerase alpha catalytic subunit Transferase C00003674 0 / 0
P21728 D(1A) dopamine receptor Dopamine receptor C00001757 0 / 0
P35354 Prostaglandin G/H synthase 2 Oxidoreductase C00001757 0 / 3
Q12809 Potassium voltage-gated channel subfamily H member 2 KCNH, Kv10-12.x (Ether-a-go-go) C00001757 2 / 2
P08246 Neutrophil elastase S1A C00001757 2 / 1
P33765 Adenosine receptor A3 Adenosine receptor C00001757 0 / 0
Q16539 Mitogen-activated protein kinase 14 p38 C00001757 0 / 0
P06746 DNA polymerase beta Enzyme C00003674 0 / 0
P49146 Neuropeptide Y receptor type 2 Neuropeptide Y receptor C00001757 0 / 0
P29466 Caspase-1 C14 C00001757 0 / 0
P17252 Protein kinase C alpha type Alpha C00001757 0 / 0
P27361 Mitogen-activated protein kinase 3 Erk C00001757 0 / 0
P14780 Matrix metalloproteinase-9 M10A C00001757 2 / 2
P02545 Prelamin-A/C Unclassified protein C00001757 11 / 10
P00918 Carbonic anhydrase 2 Lyase C00001757 1 / 2
P07550 Beta-2 adrenergic receptor Adrenergic receptor C00001757 0 / 1
P21397 Amine oxidase [flavin-containing] A Oxidoreductase C00001757 1 / 1
P25021 Histamine H2 receptor Histamine receptor C00001757 0 / 0
P35367 Histamine H1 receptor Histamine receptor C00001757 0 / 0
Q01959 Sodium-dependent dopamine transporter Dopamine C00001757 1 / 0
P08912 Muscarinic acetylcholine receptor M5 Acetylcholine receptor C00001757 0 / 0
P18825 Alpha-2C adrenergic receptor Adrenergic receptor C00001757 0 / 0
P13945 Beta-3 adrenergic receptor Adrenergic receptor C00001757 0 / 0
P34969 5-hydroxytryptamine receptor 7 Serotonin receptor C00003674 0 / 0
P25024 C-X-C chemokine receptor type 1 CXC chemokine receptor C00001757 0 / 0
P06241 Tyrosine-protein kinase Fyn Src C00001757 0 / 0
Q08209 Serine/threonine-protein phosphatase 2B catalytic subunit alpha isoform Ser_Thr C00001757 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00001757 0 / 1
P54132 Bloom syndrome protein Enzyme C00001757 1 / 2
P00533 Epidermal growth factor receptor TK tyrosine-protein kinase EGFR subfamily C00001757 1 / 8
P14416 D(2) dopamine receptor Dopamine receptor C00001757 2 / 0
P23219 Prostaglandin G/H synthase 1 Oxidoreductase C00001757 0 / 0
P37288 Vasopressin V1a receptor Vasopressin and oxytocin receptor C00001757 0 / 0
P41145 Kappa-type opioid receptor Opioid receptor C00001757 0 / 0
Q9Y271 Cysteinyl leukotriene receptor 1 Leukotriene receptor C00001757 0 / 0
P29274 Adenosine receptor A2a Adenosine receptor C00001757 0 / 0
P25929 Neuropeptide Y receptor type 1 Neuropeptide Y receptor C00001757 0 / 0
P50052 Type-2 angiotensin II receptor Angiotensin receptor C00001757 1 / 1
P17948 Vascular endothelial growth factor receptor 1 Vegfr C00001757 0 / 0
P41968 Melanocortin receptor 3 Melanocortin receptor C00001757 1 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00001757 0 / 0
P38571 Lysosomal acid lipase/cholesteryl ester hydrolase Enzyme C00001757 1 / 1
P11509 Cytochrome P450 2A6 Cytochrome P450 2A6 C00001757 0 / 0
Q16665 Hypoxia-inducible factor 1-alpha Transcription Factor C00001757 0 / 0
Q92830 Histone acetyltransferase KAT2A Enzyme C00001757 0 / 0
O75496 Geminin Unclassified protein C00001757 0 / 0
P04035 3-hydroxy-3-methylglutaryl-coenzyme A reductase Oxidoreductase C00001757 0 / 0
P08913 Alpha-2A adrenergic receptor Adrenergic receptor C00001757 0 / 0
P21917 D(4) dopamine receptor Dopamine receptor C00001757 0 / 0
P30988 Calcitonin receptor Calcitonin receptor C00001757 0 / 0
P35462 D(3) dopamine receptor Dopamine receptor C00001757 1 / 0
P41143 Delta-type opioid receptor Opioid receptor C00001757 0 / 0
Q92731 Estrogen receptor beta NR3A2 C00001757 0 / 1
P41595 5-hydroxytryptamine receptor 2B Serotonin receptor C00001757 0 / 0
P25101 Endothelin-1 receptor Endothelin receptor C00001757 0 / 0
P30411 B2 bradykinin receptor Bradykinin receptor C00001757 0 / 0
P32245 Melanocortin receptor 4 Melanocortin receptor C00001757 1 / 0
P32238 Cholecystokinin receptor type A Cholecystokinin receptor C00001757 0 / 0
P08311 Cathepsin G S1A C00001757 0 / 0
Q99720 Sigma non-opioid intracellular receptor 1 Membrane receptor C00001757 1 / 0
O00519 Fatty-acid amide hydrolase 1 Enzyme C00001757 0 / 0
P03956 Interstitial collagenase M10A C00001757 0 / 1
P32241 Vasoactive intestinal polypeptide receptor 1 Vasoactive intestinal peptide receptor C00001757 0 / 0
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00001757 0 / 0
P04150 Glucocorticoid receptor NR3C1 C00001757 0 / 1
P08172 Muscarinic acetylcholine receptor M2 Acetylcholine receptor C00001757 2 / 0
P11229 Muscarinic acetylcholine receptor M1 Acetylcholine receptor C00001757 0 / 0
P21554 Cannabinoid receptor 1 Cannabinoid receptor C00001757 0 / 0
P31645 Sodium-dependent serotonin transporter Serotonin C00001757 2 / 0
P04626 Receptor tyrosine-protein kinase erbB-2 TK tyrosine-protein kinase EGFR subfamily C00001757 5 / 9
P20309 Muscarinic acetylcholine receptor M3 Acetylcholine receptor C00001757 1 / 0
P21452 Substance-K receptor Neurokinin receptor C00001757 0 / 0
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00001757 1 / 0
P51679 C-C chemokine receptor type 4 CC chemokine receptor C00001757 0 / 0
P51681 C-C chemokine receptor type 5 CC chemokine receptor C00001757 3 / 0
P50406 5-hydroxytryptamine receptor 6 Serotonin receptor C00001757 0 / 0
P41597 C-C chemokine receptor type 2 CC chemokine receptor C00001757 1 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00001757 0 / 0
P08575 Receptor-type tyrosine-protein phosphatase C Enzyme C00001757 2 / 1
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00001757 0 / 0
O76074 cGMP-specific 3',5'-cyclic phosphodiesterase PDE_5A C00001757 0 / 0
P03372 Estrogen receptor NR3A1 C00001757 1 / 1
P08588 Beta-1 adrenergic receptor Adrenergic receptor C00001757 1 / 0
P49798 Regulator of G-protein signaling 4 Unclassified protein C00001757 2 / 0
Q16637 Survival motor neuron protein Unclassified protein C00001757 4 / 1
P28223 5-hydroxytryptamine receptor 2A Serotonin receptor C00001757 0 / 0
P28335 5-hydroxytryptamine receptor 2C Serotonin receptor C00001757 0 / 0
P35372 Mu-type opioid receptor Opioid receptor C00001757 0 / 0
P08173 Muscarinic acetylcholine receptor M4 Acetylcholine receptor C00001757 0 / 0
P25103 Substance-P receptor Neurokinin receptor C00001757 0 / 0
P25105 Platelet-activating factor receptor PAF receptor C00001757 0 / 0
P33032 Melanocortin receptor 5 Melanocortin receptor C00001757 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00001757 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00001757 0 / 1
P05181 Cytochrome P450 2E1 Cytochrome P450 2E1 C00001757 0 / 0
Q99549 M-phase phosphoprotein 8 Unclassified protein C00001757 0 / 0
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00001757 0 / 0
P23975 Sodium-dependent noradrenaline transporter Norepinephrine C00001757 1 / 1
P25100 Alpha-1D adrenergic receptor Adrenergic receptor C00001757 0 / 0
P30542 Adenosine receptor A1 Adenosine receptor C00001757 0 / 0
P18089 Alpha-2B adrenergic receptor Adrenergic receptor C00001757 0 / 0
P24557 Thromboxane-A synthase Cytochrome P450 5A1 C00001757 1 / 1
P06239 Tyrosine-protein kinase Lck Src C00001757 0 / 1
P25025 C-X-C chemokine receptor type 2 CXC chemokine receptor C00001757 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00001757 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00001757 0 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00001757 1 / 0
O00255 Menin Unclassified protein C00001757 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00001757 1 / 2
P11388 DNA topoisomerase 2-alpha Isomerase C00003674 0 / 0
Q02880 DNA topoisomerase 2-beta Isomerase C00003674 0 / 0
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00001757 0 / 0

6 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
13 AADAC, CES5A1, DAC arylacetamide deacetylase (EC:3.1.1.3) C00001757
43 ACHE, ACEE, ARACHE, N-ACHE, YT acetylcholinesterase (EC:3.1.1.7) C00001757
8824 CES2, CE-2, CES2A1, PCE-2, iCE carboxylesterase 2 (EC:3.1.1.1 3.1.1.84 3.1.1.56) C00001757
1137 CHRNA4, BFNC, EBN, EBN1, NACHR, NACHRA4, NACRA4 cholinergic receptor, nicotinic, alpha 4 (neuronal) C00001757
1141 CHRNB2, EFNL3, nAChRB2 cholinergic receptor, nicotinic, beta 2 (neuronal) C00001757
10599 SLCO1B1, HBLRR, LST-1, LST1, OATP-C, OATP1B1, OATP2, OATPC, SLC21A6 solute carrier organic anion transporter family, member 1B1 C00003674

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (58)

OMIM preferred title UniProt
#100100 Abdominal muscles, absence of, with urinary tract abnormality and cryptorchidism P20309
#103780 Alcohol dependence P08172
P14416
P31645
#614373 Amyotrophic lateral sclerosis 16, juvenile; als16 Q99720
#210900 Bloom syndrome; blm P54132
#602025 Body mass index quantitative trait locus 9; bmiq9 P41968
#300615 Brunner syndrome P21397
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#162800 Cyclic neutropenia P08246
#612522 Diabetes mellitus, insulin-dependent, 22; iddm22 P51681
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#615363 Estrogen resistance; estrr P03372
#613659 Gastric cancer P04626
#137215 Gastric cancer, hereditary diffuse; hdgc P04626
#231095 Ghosal hematodiaphyseal dysplasia; ghdd P24557
#137800 Glioma susceptibility 1; glm1 O75874
P04626
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#610140 Heart-hand syndrome, slovenian type P02545
#609423 Human immunodeficiency virus type 1, susceptibility to P41597
P51681
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#145000 Hyperparathyroidism 1; hrpt1 O00255
#603932 Intervertebral disc disease; idd P14780
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#613688 Long qt syndrome 2; lqt2 Q12809
#211980 Lung cancer P00533
P04626
#278000 Lysosomal acid lipase deficiency P38571
#608516 Major depressive disorder; mdd P08172
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
%300852 Mental retardation, x-linked 88; mrx88 P50052
#613073 Metaphyseal anadysplasia 2; mandp2 P14780
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#126200 Multiple sclerosis, susceptibility to; ms P08575
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#159900 Myoclonic dystonia P14416
#202700 Neutropenia, severe congenital, 1, autosomal dominant; scn1 P08246
#601665 Obesity P32245
#164230 Obsessive-compulsive disorder; ocd P31645
#604715 Orthostatic intolerance P23975
#259730 Osteopetrosis, autosomal recessive 3; optb3 P00918
#167000 Ovarian cancer P04626
#613135 Parkinsonism-dystonia, infantile; pkdys Q01959
#607276 Resting heart rate, variation in P08588
#275210 Restrictive dermopathy, lethal P02545
#604906 Schizophrenia 9; sczd9 P49798
#181500 Schizophrenia; sczd P49798
#608971 Severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-positive, nk cell-positive P08575
#609620 Short qt syndrome 1; sqt1 Q12809
#253300 Spinal muscular atrophy, type i; sma1 Q16637
#253550 Spinal muscular atrophy, type ii; sma2 Q16637
#253400 Spinal muscular atrophy, type iii; sma3 Q16637
#271150 Spinal muscular atrophy, type iv; sma4 Q16637
#190300 Tremor, hereditary essential, 1; etm1 P35462
#610379 West nile virus, susceptibility to P51681
#112100 Yt blood group antigen P22303

KEGG DISEASE (52)

KEGG name UniProt
H00033 Adrenal carcinoma O00255 (related)
H00034 Carcinoid O00255 (related)
H00045 Malignant islet cell carcinoma O00255 (related)
H00246 Primary hyperparathyroidism O00255 (related)
H01102 Pituitary adenomas O00255 (related)
H00016 Oral cancer P00533 (related)
P00533 (marker)
H00017 Esophageal cancer P00533 (related)
P35354 (related)
H00018 Gastric cancer P00533 (related)
P04626 (related)
H00022 Bladder cancer P00533 (related)
P04626 (related)
H00028 Choriocarcinoma P00533 (related)
P03956 (related)
P04626 (related)
H00030 Cervical cancer P00533 (related)
P04626 (related)
H00042 Glioma P00533 (related)
P00533 (marker)
H00055 Laryngeal cancer P00533 (related)
P00533 (marker)
H00241 Combined proximal and distal renal tubular acidosis (RTA type 3) P00918 (related)
H00436 Osteopetrosis P00918 (related)
H00264 Charcot-Marie-Tooth disease (CMT) P02545 (related)
H00294 Dilated cardiomyopathy (DCM) P02545 (related)
H00420 Familial partial lipodystrophy (FPL) P02545 (related)
H00563 Emery-Dreifuss muscular dystrophy P02545 (related)
H00590 Congenital muscular dystrophies (CMD/MDC) P02545 (related)
H00593 Limb-girdle muscular dystrophy (LGMD) P02545 (related)
H00601 Hutchinson-Gilford progeria syndrome P02545 (related)
H00663 Restrictive dermopathy P02545 (related)
H00665 Mandibuloacral dysplasia P02545 (related)
H01216 Left ventricular noncompaction (LVNC) P02545 (related)
H00026 Endometrial Cancer P03372 (marker)
P04626 (related)
Q92731 (marker)
H00599 46,XX disorders of sex development (Disorders related to androgen excess) P04150 (related)
H00019 Pancreatic cancer P04626 (related)
H00027 Ovarian cancer P04626 (related)
H00031 Breast cancer P04626 (related)
P04626 (marker)
H00046 Cholangiocarcinoma P04626 (related)
P35354 (related)
H00093 Combined immunodeficiencies (CIDs) P06239 (related)
H00079 Asthma P07550 (related)
H00100 Neutropenic disorders P08246 (related)
H00091 T-B+Severe combined immunodeficiencies (SCIDs) P08575 (related)
H00036 Osteosarcoma P08684 (marker)
H01205 Coumarin resistance P11712 (related)
H00025 Penile cancer P14780 (related)
P35354 (related)
H00479 Metaphyseal dysplasias P14780 (related)
H00548 Brunner syndrome P21397 (related)
H01031 Orthostatic intolerance (OI) P23975 (related)
H00490 Diaphyseal dysplasia with anemia (Ghosal) P24557 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00148 Lysosomal acid lipase deficiency P38571 (related)
H00480 Non-syndromic X-linked mental retardation P50052 (related)
H00094 DNA repair defects P54132 (related)
H00296 Defects in RecQ helicases P54132 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q03164 (related)
Q03164 (marker)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (related)
H00720 Long QT syndrome Q12809 (related)
H00725 Short QT syndrome Q12809 (related)
H00455 Spinal muscular atrophy (SMA) Q16637 (related)

Diseases related to CTD interactions

83 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D000544 Alzheimer Disease C00001757
D000647 Amnesia C00001757
D001049 Apnea C00001757
D001145 Arrhythmias, Cardiac C00001757
D001264 Athetosis C00001757
D001281 Atrial Fibrillation C00001757
D054537 Atrioventricular Block C00001757
D001919 Bradycardia C00001757
D002545 Brain Ischemia C00001757
D002375 Catalepsy C00001757
D002385 Cataplexy C00001757
D002493 Central Nervous System Diseases C00001757
D023341 Chills C00001757
D002819 Chorea C00001757
D019970 Cocaine-Related Disorders C00001757
D003072 Cognition Disorders C00001757
D003128 COMA C00001757
D003221 Confusion C00001757
D003244 Consciousness Disorders C00001757
D055191 Delayed Emergence from Anesthesia C00001757
D003693 Delirium C00001757
D003866 Depressive Disorder C00001757
D006970 Disorders of Excessive Somnolence C00001757
D062787 Drug Overdose C00001757
D064420 Drug-Related Side Effects and Adverse Reactions C00001757
D004409 Dyskinesia, Drug-Induced C00001757
D004421 Dystonia C00001757
D020821 Dystonic Disorders C00001757
D004831 Epilepsies, Myoclonic C00001757
D005207 Fasciculation C00001757
D005334 Fever C00001757
D015812 Glaucoma, Angle-Closure C00001757
D006212 Hallucinations C00001757
D006323 Heart Arrest C00001757
D006816 Huntington Disease C00001757
D006948 Hyperkinesis C00001757
D006973 Hypertension C00001757
D007008 Hypokalemia C00001757
D007022 Hypotension C00001757
D007024 Hypotension, Orthostatic C00001757
D007035 Hypothermia C00001757
D007247 Infertility, Female C00001757
D007859 Learning Disorders C00001757
D053609 Lethargy C00001757
D008325 Mammary Neoplasms, Experimental C00001757
D008569 Memory Disorders C00001757
D001523 Mental Disorders C00001757
D015877 Miosis C00001757
D019964 Mood Disorders C00001757
D009069 Movement Disorders C00001757
D015878 Mydriasis C00001757
D009207 Myoclonus C00001757
D009325 Nausea C00001757
D009461 Neurologic Manifestations C00001757
D009759 Nystagmus, Pathologic C00001757
D009886 Ophthalmoplegia C00001757
D010146 Pain C00001757
D010554 Personality Disorders C00001757
D010939 Plant Poisoning C00001757
D011041 Poisoning C00001757
D011183 Postoperative Complications C00001757
D020250 Postoperative Nausea and Vomiting C00001757
D011595 Psychomotor Agitation C00001757
D011596 Psychomotor Disorders C00001757
D011605 Psychoses, Substance-Induced C00001757
D012131 Respiratory Insufficiency C00001757
D012640 Seizures C00001757
D012798 Sialorrhea C00001757
D020181 Sleep Apnea, Obstructive C00001757
D013064 Speech Disorders C00001757
D013132 Spinocerebellar Degenerations C00001757
D013226 Status Epilepticus C00001757
D053608 Stupor C00001757
D013375 Substance Withdrawal Syndrome C00001757
D013610 Tachycardia C00001757
D013616 Tachycardia, Sinus C00001757
D017180 Tachycardia, Ventricular C00001757
D016171 Torsades de Pointes C00001757
D014202 Tremor C00001757
D014474 Unconsciousness C00001757
D014693 Ventricular Fibrillation C00001757
D014839 Vomiting C00001757
D014987 Xerostomia C00001757