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FLUGRAN-5MG
(10)
FLUNARIZINE-5MG
ANTI-MIGRANE DRUGS
NEPAL PHARMACEUTICAL LAB-LAPEN DIVISON
Product Details
Flunarizine
Flunarizine is a selective calcium entry blocker with calmodulin binding properties and histamine H1 blocking activity. It is effective in the prophylaxis of migraine, occlusive peripheral vascular disease, vertigo of central and peripheral origin, and as an adjuvant in the therapy of epilepsy.
Indication
Used in the prophylaxis of migraine, occlusive peripheral vascular disease, vertigo of central and peripheral origin, and as an adjuvant in the therapy of epilepsy.
Associated Conditions
Pharmacodynamics
Flunarizine is a selective calcium entry blocker with calmodulin binding properties and histamine H1 blocking activity.
Mechanism of action
Flunarizine inhibits the influx of extracellular calcium through myocardial and vascular membrane pores by physically plugging the channel. The decrease in intracellular calcium inhibits the contractile processes of smooth muscle cells, causing dilation of the coronary and systemic arteries, increased oxygen delivery to the myocardial tissue, decreased total peripheral resistance, decreased systemic blood pressure, and decreased afterload.
Absorption
85% following oral administration.
Volume of distribution
Not Available
Protein binding
99% bound to plasma proteins
Metabolism
Hepatic, to two metabolites via N-dealylation and hydroxylation.
- Flunarizine
- Flunarizine
- Flunarizine
Route of elimination
Not Available
Half life
18 days
Clearance
Not Available
Toxicity
-Flunarizine should be used with care in patients with depression or those being prescribed other agents, such as phenothiazines, concurrently, which may cause extrapyramidal side-effects. -Acute overdosage has been reported and the observed symptoms were sedation, agitation and tachycardia. -Treatment of acute overdosage consists of charcoal administration, induction of emesis or gastric lavage, and supportive measures. No specific antidote is known.
Affected organisms
- Humans and other mammals
source: drugbank