MetaADEDB 2.0 @ LMMD
Nitroxyl
(ODUCDPQEXGNKDN-UHFFFAOYSA-N)
Structure
SMILES
N=O
Molecular Formula:
HNO
Molecular Weight:
31.014
Log P:
0.4313
Hydrogen Bond Acceptor:
2
Hydrogen Bond Donor:
1
TPSA:
40.92
CAS Number(s):
11129-69-4; 14332-28-6
Synonym(s)
1.
Nitroxyl
External Link(s)
PubChem Compound945
ChEBI84879
KEGGcpd:C20937
Adverse Drug Event(s)
NameNumber of ReportsReference(s)Data Source
1Device FailureFAERS: 30
Canada Vigilance: 2
Canada Vigilance
US FAERS
2Cardiac ArrestFAERS: 17
Canada Vigilance: 2
Canada Vigilance
US FAERS
3Device malfunctionFAERS: 16US FAERS
4General physical health deteriorationFAERS: 13US FAERS
5Occupational exposure to productFAERS: 12US FAERS
6Product use issueFAERS: 11
Canada Vigilance: 3
Canada Vigilance
US FAERS
7Drug ineffective for unapproved indicationFAERS: 9
Canada Vigilance: 2
Canada Vigilance
US FAERS
8Medication ErrorFAERS: 8
Canada Vigilance: 2
Canada Vigilance
US FAERS
9No adverse eventFAERS: 8US FAERS
10Drug ineffectiveFAERS: 7
Canada Vigilance: 2
Canada Vigilance
US FAERS
11Medical device complicationFAERS: 7US FAERS
12PneumothoraxFAERS: 7US FAERS
13HypotensionFAERS: 6US FAERS
14BradycardiaFAERS: 5US FAERS
15HeadacheFAERS: 5US FAERS
16NauseaFAERS: 5US FAERS
17Respiratory FailureFAERS: 5US FAERS
18SepsisFAERS: 5US FAERS
19HypoxiaFAERS: 4US FAERS
20Pulmonary EmbolismFAERS: 4US FAERS
21Chest discomfortFAERS: 3US FAERS
22DizzinessFAERS: 3US FAERS
23PneumoniaFAERS: 3US FAERS
24Pulmonary HypertensionFAERS: 3US FAERS
25Pulmonary arterial pressure increasedFAERS: 3US FAERS
26Right ventricular failureFAERS: 3US FAERS
27ShockFAERS: 3US FAERS
28Ventricular FibrillationFAERS: 3US FAERS
29Wrong drug administeredFAERS: 3US FAERS
30Device alarm issueFAERS: 2US FAERS
31Device leakageFAERS: 2US FAERS
32Disease ProgressionFAERS: 2US FAERS
33Disseminated Intravascular CoagulationFAERS: 2US FAERS
34Drug administered to patient of inappropriate ageFAERS: 2US FAERS
35Drug administration errorFAERS: 2US FAERS
36Drug delivery system malfunctionFAERS: 2US FAERS
37EndocarditisFAERS: 2US FAERS
38Intestinal PerforationFAERS: 2US FAERS
39Neonatal disorderFAERS: 2US FAERS
40Neonatal respiratory arrestFAERS: 2US FAERS
41Neonatal respiratory failureFAERS: 2US FAERS
42PainFAERS: 2US FAERS
43Product use in unapproved indicationFAERS: 2US FAERS
44Rebound effectFAERS: 2
Canada Vigilance: 1
Canada Vigilance
US FAERS
45Therapeutic response unexpectedFAERS: 2US FAERS
46Therapy cessationFAERS: 2US FAERS
47Therapy non-responderFAERS: 2
Canada Vigilance: 2
Canada Vigilance
US FAERS
48ThrombocytopeniaFAERS: 2US FAERS
49Unresponsive to stimuliFAERS: 2US FAERS
50Withdrawal of life supportFAERS: 2
Canada Vigilance: 3
Canada Vigilance
US FAERS
51Wrong technique in device usage processFAERS: 2US FAERS
52Accidental exposure to productFAERS: 1US FAERS
53Accidental exposureFAERS: 1US FAERS
54Accidental overdoseFAERS: 1US FAERS
55Acute kidney injuryFAERS: 1
Canada Vigilance: 1
Canada Vigilance
US FAERS
56Alveolar capillary dysplasiaFAERS: 1US FAERS
57Anaphylactic shockFAERS: 1US FAERS
58AnoxiaFAERS: 1US FAERS
59AstheniaFAERS: 1US FAERS
60Atrial FibrillationFAERS: 1US FAERS
61Bacterial sepsisFAERS: 1US FAERS
62Blood pH decreasedFAERS: 1US FAERS
63Brain DeathFAERS: 1US FAERS
64BronchitisFAERS: 1US FAERS
65Bronchopulmonary DysplasiaFAERS: 1US FAERS
66Complication of device insertionFAERS: 1US FAERS
67DermatomyositisFAERS: 1US FAERS
68Device connection issueFAERS: 1US FAERS
69Device deployment issueFAERS: 1US FAERS
70Device information output issueFAERS: 1US FAERS
71Device use errorFAERS: 1US FAERS
72Drug exposure during pregnancyFAERS: 1US FAERS
73DysarthriaFAERS: 1US FAERS
74EpistaxisFAERS: 1US FAERS
75ErythemaFAERS: 1US FAERS
76Hepatic congestionFAERS: 1US FAERS
77Idiopathic Pulmonary FibrosisFAERS: 1US FAERS
78Incorrect dose administered by deviceFAERS: 1US FAERS
79InfluenzaFAERS: 1US FAERS
80MalaiseFAERS: 1US FAERS
81Metabolic acidosisFAERS: 1US FAERS
82OliguriaFAERS: 1
Canada Vigilance: 1
Canada Vigilance
US FAERS
83Post procedural complicationFAERS: 1US FAERS
84Procedural complicationFAERS: 1US FAERS
85Product quality issueFAERS: 1US FAERS
86Product used for unknown indicationFAERS: 1US FAERS
87Pulmonary hypertensive crisisFAERS: 1US FAERS
88Respiratory tract infection viralFAERS: 1US FAERS
89Right Ventricular DysfunctionFAERS: 1US FAERS
90Right Ventricular HypertrophyFAERS: 1US FAERS
91Septic ShockFAERS: 1US FAERS
92Stenotrophomonas infectionFAERS: 1US FAERS
93Subcutaneous EmphysemaFAERS: 1US FAERS
94TachycardiaFAERS: 1US FAERS
95Therapeutic product effect incompleteFAERS: 1US FAERS
96Therapeutic product ineffective for unapproved indicationFAERS: 1US FAERS
97Throat irritationFAERS: 1US FAERS
98Toxic Shock SyndromeFAERS: 1US FAERS
99Wrong technique in product usage processFAERS: 1
Canada Vigilance: 1
Canada Vigilance
US FAERS
100Product complaintCanada Vigilance: 1Canada Vigilance
101Product packaging issueCanada Vigilance: 1Canada Vigilance
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