Prophylaxis of migraine, Vertigo and vestibular disorders
Adult: 10 mg daily in the evening.
Elderly: ≥65 years 5 mg daily in the evening.
Elderly: ≥65 years 5 mg daily in the evening.
Indications and Dosage
Oral
Prophylaxis of migraine, Vertigo and vestibular disorders Adult: 10 mg daily in the evening.
Elderly: ≥65 years 5 mg daily in the evening. |
Administration
May be taken with or without food.
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Contraindications
History of depression, pre-existing symptoms of Parkinson’s disease, other extrapyramidal disorders.
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Special Precautions
Hepatic impairment. Elderly. Pregnancy and lactation.
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Adverse Reactions
Significant: Depression, increased serum prolactin, menstrual irregularities, extrapyramidal symptoms. Rarely,: progressive fatigue, galactorrhoea.
Gastrointestinal disorders: Nausea, vomiting, constipation, stomach pain. Investigations: Weight gain. Metabolism and nutrition disorders: Increased appetite. Musculoskeletal and connective tissue disorders: Myalgia. Nervous system disorders: Drowsiness, somnolence. Psychiatric disorders: Insomnia. Respiratory, thoracic and mediastinal disorders: Rhinitis. |
Patient Counseling Information
This drug may cause somnolence, if affected, do not drive or operate machinery.
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MonitoringParameters
Monitor for extrapyramidal, depressive, and fatigue symptoms.
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Overdosage
Symptoms: Sedation, asthenia, agitation, tachycardia. Management. May give activated charcoal if considered appropriate.
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Drug Interactions
Increases sedative effect with hypnotics and tranquillisers. Decreased plasma concentration with phenytoin, carbamazepine.
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Food Interaction
Increases sedative effect with alcohol.
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Action
Description: Flunarizine is a difluorinated derivative of cinnarizine. It has selective calcium-channel blocking activity, sedative and antihistamine properties, and has no effect on heart contractility or conduction.
Pharmacokinetics: Absorption: Well absorbed from the gastrointestinal tract. Time to peak plasma concentration: 2-4 hours. Distribution: Volume of distribution: 43.2 L/kg. Plasma protein binding: >90%. Metabolism: Extensively metabolised in the liver via N-oxidation and aromatic hydroxylation. Excretion: Mainly via faeces (<6%); urine (minimal). Elimination half-life: Approx 18 hours. |
Chemical Structure
![]() Source: National Center for Biotechnology Information. PubChem Compound Summary for CID 941361, Flunarizine. https://pubchem.ncbi.nlm.nih.gov/compound/Flunarizine. Accessed Sept. 24, 2020. |
Storage
Store between 15-30°C. Protect from light and moisture.
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ATC Classification
N07CA03 - flunarizine ; Belongs to the class of antivertigo preparations.
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References
Anon. Flunarizine. Lexicomp Online. Hudson, Ohio. Wolters Kluwer Clinical Drug Information, Inc. https://online.lexi.com. Accessed 05/08/2020. Buckingham R (ed). Flunarizine Hydrochloride. Martindale: The Complete Drug Reference [online]. London. Pharmaceutical Press. https://www.medicinescomplete.com. Accessed 05/08/2020. Flumig (Unison). MIMS Philippines. http://www.mims.com/philippines. Accessed 05/08/2020. Sibelium (Johnson & Johnson Sdn Bhd). National Pharmaceutical Regulatory Agency - Ministry of Health Malaysia. https://www.npra.gov.my/. Accessed 05/08/2020.
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