Mechanism of Action
LAMISIL Tablets is a prescription medicine used to treat fungal infections of the fingernails and toenails (onychomycosis)
MECHANISM OF ACTION An allylamine that inhibits squalene epoxidase, an enzyme involved in the biosynthesis of ergosterol, an essential component of fungal cell
Synthetic allylamine derivative that inhibits squalene epoxidase, a key enzyme in sterol biosynthesis in fungi
terbinafine (Lamisil) Pharmacy Author: Omudhome Ogbru, PharmD Medical and Pharmacy Editor: Jay W
Terbinafine (Lamisil®) has primary fungicidal action against many fungi as a result of its specific mechanism of squalene epoxidase inhibition
24 to 72 hours
Rats given oxycodone during lactation showed smaller offspring, though after lactation, they recovered to normal size
2 Schizophrenia is a mental illness characterized by positive (such as hallucinations LamISIL AT: 1% (12 g, 24 g [DSC], 30 g, 36 g [DSC], 42 g) [contains benzyl alcohol, cetyl alcohol] Mechanism of Action
5 Corticosteroids binding to the glucocorticoid receptor mediates changes in gene expression that lead to multiple downstream effects over hours to days
3
Lamisil Tablets are not recommended for patients with chronic or active liver disease
When ergosterol synthesis becomes inhibited, the
Rather, aspirin is the only NSAID that irreversibly inhibits COX-1
Mechanism of action
[1] In comparison, a mechanism of action (MOA) describes such changes at the molecular level
Tioconazole is an imidazole antifungal used to treat fungal and yeast infections
3 It can effectively manage acute pain as well as pain related to rheumatic diseases, and has a well studied
Revised: 12/2023
Terbinafine is an allylamine antifungal [see Clinical Lamisil 1% 10mg/ml Topical Spray manufactured by Novartis Consumer Health SA
Lamisil is classified as an allylamine antifungal, while Miconazole belongs to the imidazole antifungal group
Oral doses of terbinafine hydrochloride up to 300 mg/kg/day (in terms of mg/m 2 /day equivalent to 146 and 329 times the maximum potential exposure at the recommended topical human dose*) during organogenesis in rats and rabbits, respectively, were not teratogenic
Furosemide promotes diuresis by blocking tubular reabsorption of sodium and chloride in the proximal and distal tubules
5 This action leads to a reduction in uterine weight and elevated leuteinizing hormone