Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Nimodipine
Drug ID BADD_D01569
Description Nimodipine is a 1,4-dihydropyridine calcium channel blocker. It acts primarily on vascular smooth muscle cells by stabilizing voltage-gated L-type calcium channels in their inactive conformation. By inhibiting the influx of calcium in smooth muscle cells, nimodipine prevents calcium-dependent smooth muscle contraction and subsequent vasoconstriction. Compared to other calcium channel blocking agents, nimodipine exhibits greater effects on cerebral circulation than on peripheral circulation. Nimodipine is used to as an adjunct to improve the neurologic outcome following subarachnoid hemorrhage from ruptured intracranial aneurysm.
Indications and Usage For use as an adjunct to improve neurologic outcome following subarachnoid hemorrhage (SAH) from ruptured intracranial berry aneurysms by reducing the incidence and severity of ischemic deficits.
Marketing Status approved; investigational
ATC Code C08CA06
DrugBank ID DB00393
KEGG ID D00438
MeSH ID D009553
PubChem ID 4497
TTD Drug ID D0XN1F
NDC Product Code 70966-0012; 49452-4854; 63739-797; 43898-0117; 62973-300; 68084-912; 10888-8124; 65655-0012; 58624-0495; 23155-512; 67877-297; 69452-209; 10888-8113; 58159-047; 76055-0047; 24338-230; 24338-260
UNII 57WA9QZ5WH
Synonyms Nimodipine | Bay e 9736 | e 9736, Bay | Brainal | Calnit | Kenesil | Nymalize | Nimodipin Hexal | Hexal, Nimodipin | Nimodipin-ISIS | Nimodipin ISIS | Nimodipino Bayvit | Bayvit, Nimodipino | Nimotop | Remontal | Admon | Modus
Chemical Information
Molecular Formula C21H26N2O7
CAS Registry Number 66085-59-4
SMILES CC1=C(C(C(=C(N1)C)C(=O)OC(C)C)C2=CC(=CC=C2)[N+](=O)[O-])C(=O)OCCOC
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)
Hyponatraemia14.05.04.002--
Hypotension24.06.03.0020.000067%
Ileus07.13.01.001--
Immune system disorder10.02.01.001--Not Available
Intracranial pressure increased17.07.02.0020.000084%Not Available
Jaundice23.03.03.030; 09.01.01.004; 01.06.04.004--Not Available
Liver function test abnormal13.03.04.030--Not Available
Muscle spasms15.05.03.004--
Myalgia15.05.02.001--
Nausea07.01.07.001--
Nervous system disorder17.02.10.001--Not Available
Oedema14.05.06.010; 08.01.07.006--Not Available
Palpitations02.11.04.012--
Phlebitis24.12.03.004; 12.02.01.002--
Platelet count decreased13.01.04.001--
Pruritus23.03.12.001--
Rash23.03.13.001--Not Available
Seizure17.12.03.0010.000151%
Subarachnoid haemorrhage24.07.04.004; 17.08.01.010; 12.01.10.011--Not Available
Tachycardia02.03.02.007--Not Available
Thrombocytopenia01.08.01.002--Not Available
Toxic epidermal necrolysis12.03.01.015; 11.07.01.006; 10.01.01.006; 23.03.01.0080.000034%
Vasospasm24.04.02.002--Not Available
Vomiting07.01.07.003--
Wheezing22.03.01.009--
Deep vein thrombosis24.01.02.003--Not Available
Lymphatic disorder01.09.01.003--Not Available
Musculoskeletal discomfort15.03.04.001--Not Available
Infusion site reaction12.07.05.006; 08.02.05.005--Not Available
Angiopathy24.03.02.007--Not Available
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