Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Enoxaparin sodium
Drug ID BADD_D00772
Description Not Available
Indications and Usage Not Available
Marketing Status Not Available
ATC Code Not Available
DrugBank ID Not Available
KEGG ID D03674
MeSH ID C000711671
PubChem ID 60196282
TTD Drug ID D01ZJK
NDC Product Code 81952-132; 0955-1004; 11797-763; 0075-0623; 0075-2915; 60505-0793; 63323-564; 63323-586; 63323-589; 71288-433; 0781-3256; 0781-3262; 81952-123; 0075-0622; 0075-8013; 16714-056; 60505-0791; 68001-460; 0548-5601; 71288-438; 0703-8530; 11797-761; 11797-762; 0075-0624; 0075-8018; 60505-0794; 63323-607; 63323-609; 68001-464; 70710-1761; 0548-5602; 71288-426; 71839-109; 55154-4028; 60505-0795; 63323-531; 63323-559; 63323-605; 68001-459; 70710-1760; 0548-5603; 71839-115; 81952-128; 0955-1012; 0955-1016; 0075-8022; 55154-3540; 55154-3543; 60505-0798; 63323-584; 68001-457; 68001-458; 68001-462; 70710-1757; 71288-411; 71288-435; 71288-436; 71288-437; 71839-112; 0955-1008; 11797-757; 0075-0620; 0075-8014; 16714-066; 63323-533; 63323-537; 63323-566; 71288-432; 0703-8510; 0781-3238; 19657-0001; 43796-200; 11797-760; 0075-0621; 0075-2912; 55154-6689; 63323-539; 68001-463; 0548-5607; 71839-116; 0781-3246; 0781-3268; 0781-3298; 81952-124; 19657-0003; 28955-002; 0955-1015; 0075-8025; 55154-3541; 60505-0796; 63323-535; 0548-5604; 0548-5608; 0781-3299; 81952-135; 0955-1003; 0955-1006; 62255-1325; 67957-0003; 0075-8020; 16714-016; 16714-026; 16714-046; 55154-3542; 55154-6690; 55154-6692; 60505-0792; 70710-1758; 70710-1759; 0548-5606; 71288-434; 71839-110; 71839-111; 71839-113; 0703-8540; 81952-126; 0075-0626; 0075-8016; 0075-8030; 16714-006; 63323-655; 68001-461; 70710-1762; 70710-1763; 0548-5605; 71288-410; 76420-086; 81952-130; 0955-1010; 11797-758; 11797-759; 16714-036; 55154-3544
UNII 8NZ41MIK1O
Synonyms enoxaparin sodium | RP 54563
Chemical Information
Molecular Formula C42H59N3Na4O35S2
CAS Registry Number 679809-58-6
SMILES CC1C(C(OC(C1OC2CC(C(C(C2O)O)OC3C(C(C(C(O3)COS(=O)(=O)O)OC4C(C(C=C(O4)C(=O)[O-])O )O)O)NC(=O)C)C(=O)[O-])CO)OC5C(C(C(OC5C(=O)[O-])OC6C7COC(O7)C(C6O)NS(=O)(=O)[O-] )O)O)NC(=O)C.[Na+].[Na+].[Na+].[Na+]
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)
Alanine aminotransferase increased13.03.04.005--
Anaemia01.03.02.001--
Anaphylactoid reaction24.06.03.007; 10.01.07.003--Not Available
Aspartate aminotransferase increased13.03.04.011--
Atrial fibrillation02.03.03.002--
Cardiac failure02.05.01.001--
Confusional state19.13.01.001; 17.02.03.005--
Cutaneous vasculitis24.12.04.008; 23.06.02.001; 10.02.02.003--Not Available
Dermatitis bullous23.03.01.002--
Diarrhoea07.02.01.001--
Dyspnoea22.02.01.004; 02.11.05.003--
Ecchymosis24.07.06.002; 23.06.01.001; 01.01.03.001--Not Available
Epidural anaesthesia25.01.03.004--Not Available
Erythema23.03.06.001--Not Available
Extradural haematoma17.08.05.001; 12.01.10.002; 24.07.04.002--Not Available
Haematoma24.07.01.001--
Haematuria21.10.01.018; 24.07.01.047; 20.02.01.006--
Hyperkalaemia14.05.03.001--
Hypersensitivity10.01.03.003--
Injection site haemorrhage24.07.01.010; 12.07.03.005; 08.02.03.005--Not Available
Injection site pain12.07.03.011; 08.02.03.010--Not Available
Nausea07.01.07.001--
Nervous system disorder17.02.10.001--Not Available
Oedema14.05.06.010; 08.01.07.006--Not Available
Oedema peripheral14.05.06.011; 08.01.07.007; 02.05.04.007--
Pain08.01.08.004--
Pneumonia22.07.01.003; 11.01.09.003--Not Available
Pruritus23.03.12.001--
Pulmonary oedema22.01.03.003; 02.05.02.003--
Purpura24.07.06.005; 23.06.01.004; 01.01.04.003--
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