Peringatan Keamanan

The reported LD50 of oral atorvastatin in mice is higher than 5000 mg/kg.MSDS In cases of overdose with atorvastatin, there is reported symptoms of complicated breathing, jaundice, liver damage, dark urine, muscle pain, and seizures.L6031 In case of overdose, symptomatic treatment is recommended and due to the high plasma protein binding, hemodialysis is not expected to generate significant improvement.FDA label

In carcinogenic studies with high doses of atorvastatin, evidence of rhabdomyosarcoma, fibrosarcoma, liver adenoma, and liver carcinoma were observed.FDA label

In fertility studies with high doses of atorvastatin, there were events of aplasia, aspermia, low testis and epididymal weight, decreased sperm motility, decreased spermatid head concentration and increased abnormal sperm.FDA label

Atorvastatin was shown to not be mutagenic in diverse mutagenic assays.FDA label

Atorvastatin

DB01076

small molecule approved

Deskripsi

Atorvastatin (Lipitor®), is a lipid-lowering drug included in the statin class of medications. By inhibiting the endogenous production of cholesterol in the liver, statins lower abnormal cholesterol and lipid levels, and ultimately reduce the risk of cardiovascular disease. More specifically, statin medications competitively inhibit the enzyme hydroxymethylglutaryl-coenzyme A (HMG-CoA) Reductase,A181421 which catalyzes the conversion of HMG-CoA to mevalonic acid. This conversion is a critical metabolic reaction involved in the production of several compounds involved in lipid metabolism and transport, including cholesterol, low-density lipoprotein (LDL) (sometimes referred to as "bad cholesterol"), and very-low-density lipoprotein (VLDL). Prescribing statins is considered standard practice for patients following any cardiovascular event, and for people who are at moderate to high risk of developing cardiovascular disease. The evidence supporting statin use, coupled with minimal side effects and long term benefits, has resulted in wide use of this medication in North America.A181087, A181406

Atorvastatin and other statins including lovastatin, pravastatin, rosuvastatin, fluvastatin, and simvastatin are considered first-line treatment options for dyslipidemia.A181087, A181406 The increasing use of this class of drugs is largely attributed to the rise in cardiovascular diseases (CVD) (such as heart attack, atherosclerosis, angina, peripheral artery disease, and stroke) in many countries.A181084 An elevated cholesterol level (elevated low-density lipoprotein (LDL) levels in particular) is a significant risk factor for the development of CVD.A181087,A181553 Several landmark studies demonstrate that the use of statins is associated with both a reduction in LDL levels and CVD risk.A181090,A181093,A181096,A181427,A181475,A181538 Statins were shown to reduce the incidences of all-cause mortality, including fatal and non-fatal CVD, as well as the need for surgical revascularization or angioplasty following a heart attack.A181087, A181406 Some evidence has shown that even for low-risk individuals (with <10% risk of a major vascular event occurring within five years) statin use leads to a 20%-22% relative reduction in the number of major cardiovascular events (heart attack, stroke, coronary revascularization, and coronary death) for every 1 mmol/L reduction in LDL without any significant side effects or risks.A181397, A181403

Atorvastatin was first synthesized in 1985 by Dr. Bruce Roth and approved by the FDA in 1996.T568 It is a pentasubstituted pyrrole A177415 formed by two contrasting moieties with an achiral heterocyclic core unit and a 3,5-dihydroxypentanoyl side chain identical to its parent compound.T571 Unlike other members of the statin group, atorvastatin is an active compound and therefore does not require activation.A177436

Struktur Molekul 2D

Berat 558.6398
Wujud solid

Peta Jejaring Molekuler
Legenda: ObatTargetGenEnzim(Panah → menunjukkan arah efek / relasi)TransporterCarrier

Profil Farmakokinetik

Waktu Paruh (Half-Life) The half-life of atorvastatin is 14 hours while the half-life of its metabolites can reach up to 30 hours.[F4670,F4673]
Volume Distribusi The reported volume of distribution of atorvastatin is of 380 L.[F4670,F4673]
Klirens (Clearance) The registered total plasma clearance of atorvastatin is of 625 ml/min.[A19474]

Absorpsi

Atorvastatin presents a dose-dependent and non-linear pharmacokinetic profile.A177436 It is very rapidly absorbed after oral administration. After the administration of a dose of 40 mg, its peak plasma concentration of 28 ng/ml is reached 1-2 hours after initial administration with an AUC of about 200 ng?h/ml.A177478 Atorvastatin undergoes extensive first-pass metabolism in the wall of the gut and the liver, resulting in an absolute oral bioavailability of 14%.A177397 Plasma atorvastatin concentrations are lower (approximately 30% for Cmax and AUC) following evening drug administration compared with morning. However, LDL-C reduction is the same regardless of the time of day of drug administration.F4670 Administration of atorvastatin with food results in prolonged Tmax and a reduction in Cmax and AUC.A177415 Breast Cancer Resistance Protein (BCRP) is a membrane-bound protein that plays an important role in the absorption of atorvastatin.A181460 Evidence from pharmacogenetic studies of c.421C>A single nucleotide polymorphisms (SNPs) in the gene for BCRP has demonstrated that individuals with the 421AA genotype have reduced functional activity and 1.72-fold higher AUC for atorvastatin compared to study individuals with the control 421CC genotype. This has important implications for the variation in response to the drug in terms of efficacy and toxicity, particularly as the BCRP c.421C>A polymorphism occurs more frequently in Asian populations than in Caucasians.A181478, A181487 Other statin drugs impacted by this polymorphism include fluvastatin, simvastatin, and rosuvastatin.A181478 Genetic differences in the OATP1B1 (organic-anion-transporting polypeptide 1B1) hepatic transporter encoded by the SCLCO1B1 gene (Solute Carrier Organic Anion Transporter family member 1B1) have been shown to impact atorvastatin pharmacokinetics. Evidence from pharmacogenetic studies of the c.521T>C single nucleotide polymorphism (SNP) in the gene encoding OATP1B1 (SLCO1B1) demonstrated that atorvastatin AUC was increased 2.45-fold for individuals homozygous for 521CC compared to homozygous 521TT individuals.A181493 Other statin drugs impacted by this polymorphism include simvastatin, pitavastatin, rosuvastatin, and pravastatin.A181460

Metabolisme

Atorvastatin is highly metabolized to ortho- and parahydroxylated derivatives and various beta-oxidation products, primarily by Cytochrome P450 3A4 in the intestine and liver.F4670,F4673 Atorvastatin's metabolites undergo further lactonization via the formation of acyl glucuronide intermediates by the enzymes UGT1A1 and UGT1A3. These lactones can be hydrolyzed back to their corresponding acid forms and exist in equilibirum.A19474,A181460 In vitro inhibition of HMG-CoA reductase by ortho- and parahydroxylated metabolites is equivalent to that of atorvastatin. Approximately 70% of circulating inhibitory activity for HMG-CoA reductase is attributed to active metabolites.F4670,F4673

Rute Eliminasi

Atorvastatin and its metabolites are mainly eliminated in the bile without enterohepatic recirculation. The renal elimination of atorvastatin is very minimal and represents less than 1% of the eliminated dose.F4670,F4673

Farmakogenomik

3 Varian
KIF6 (rs20455)

Patients with this genotype have a greater reduction in risk of a major cardiovascular event with high dose atorvastatin.

HMGCR (rs17244841)

Patients with this genotype have a lesser reduction in LDL cholesterol with atorvastatin.

CYP3A4 (rs2740574)

Patients with this genotype have an greater reduction in LDL cholesterol with atorvastatin.

Interaksi Makanan

2 Data
  • 1. Avoid grapefruit products. Grapefruit products may increase the risk for atorvastatin related adverse effects such as myopathy and rhabdomyolysis.
  • 2. Take with or without food. Food decreases absorption but not to a clinically significant extent.

Interaksi Obat

753 Data
Cyclosporine The excretion of Atorvastatin can be decreased when combined with Cyclosporine.
Reserpine Reserpine may decrease the excretion rate of Atorvastatin which could result in a higher serum level.
Ursodeoxycholic acid Ursodeoxycholic acid may decrease the excretion rate of Atorvastatin which could result in a higher serum level.
Cholic Acid Cholic Acid may decrease the excretion rate of Atorvastatin which could result in a higher serum level.
Valinomycin Valinomycin may decrease the excretion rate of Atorvastatin which could result in a higher serum level.
Troglitazone Troglitazone may decrease the excretion rate of Atorvastatin which could result in a higher serum level.
Progesterone Progesterone may decrease the excretion rate of Atorvastatin which could result in a higher serum level.
Celecoxib Celecoxib may decrease the excretion rate of Atorvastatin which could result in a higher serum level.
Chlorpromazine Chlorpromazine may decrease the excretion rate of Atorvastatin which could result in a higher serum level.
Olmesartan Olmesartan may decrease the excretion rate of Atorvastatin which could result in a higher serum level.
Nifedipine Atorvastatin may decrease the excretion rate of Nifedipine which could result in a higher serum level.
Lenvatinib Lenvatinib may decrease the excretion rate of Atorvastatin which could result in a higher serum level.
Acipimox Acipimox may increase the myopathic rhabdomyolysis activities of Atorvastatin.
Bezafibrate Bezafibrate may increase the myopathic rhabdomyolysis activities of Atorvastatin.
Ciprofibrate The risk or severity of myopathy, rhabdomyolysis, and myoglobinuria can be increased when Ciprofibrate is combined with Atorvastatin.
Daptomycin The risk or severity of myopathy can be increased when Atorvastatin is combined with Daptomycin.
Gemfibrozil The risk or severity of rhabdomyolysis, myoglobinuria, and elevated creatine kinase (CPK) can be increased when Gemfibrozil is combined with Atorvastatin.
Niacin The risk or severity of myopathy and rhabdomyolysis can be increased when Niacin is combined with Atorvastatin.
Raltegravir The risk or severity of myopathy and rhabdomyolysis can be increased when Raltegravir is combined with Atorvastatin.
Trabectedin The risk or severity of myopathy and rhabdomyolysis can be increased when Atorvastatin is combined with Trabectedin.
Fluconazole The metabolism of Atorvastatin can be decreased when combined with Fluconazole.
Erythromycin The serum concentration of Atorvastatin can be increased when it is combined with Erythromycin.
Azithromycin The risk or severity of myopathy and rhabdomyolysis can be increased when Azithromycin is combined with Atorvastatin.
Bosentan The serum concentration of Atorvastatin can be decreased when it is combined with Bosentan.
Danazol The serum concentration of Atorvastatin can be increased when it is combined with Danazol.
Quinine The risk or severity of myopathy and rhabdomyolysis can be increased when Quinine is combined with Atorvastatin.
Quinidine The risk or severity of myopathy and rhabdomyolysis can be increased when Quinidine is combined with Atorvastatin.
Ranolazine The serum concentration of Atorvastatin can be increased when it is combined with Ranolazine.
Bexarotene The serum concentration of Atorvastatin can be decreased when it is combined with Bexarotene.
Diltiazem The serum concentration of Diltiazem can be increased when it is combined with Atorvastatin.
Colestipol Colestipol can cause a decrease in the absorption of Atorvastatin resulting in a reduced serum concentration and potentially a decrease in efficacy.
Sevelamer Sevelamer can cause a decrease in the absorption of Atorvastatin resulting in a reduced serum concentration and potentially a decrease in efficacy.
Colesevelam Colesevelam can cause a decrease in the absorption of Atorvastatin resulting in a reduced serum concentration and potentially a decrease in efficacy.
Cholestyramine Cholestyramine can cause a decrease in the absorption of Atorvastatin resulting in a reduced serum concentration and potentially a decrease in efficacy.
Digoxin The serum concentration of Digoxin can be increased when it is combined with Atorvastatin.
Metildigoxin The serum concentration of Metildigoxin can be increased when it is combined with Atorvastatin.
Acetyldigoxin The serum concentration of Acetyldigoxin can be increased when it is combined with Atorvastatin.
Mifepristone The serum concentration of Atorvastatin can be increased when it is combined with Mifepristone.
Verapamil The serum concentration of Verapamil can be increased when it is combined with Atorvastatin.
Midazolam The serum concentration of Midazolam can be increased when it is combined with Atorvastatin.
Lamotrigine The metabolism of Atorvastatin can be increased when combined with Lamotrigine.
Desogestrel The metabolism of Atorvastatin can be increased when combined with Desogestrel.
Testosterone propionate The metabolism of Atorvastatin can be increased when combined with Testosterone propionate.
Tipranavir The serum concentration of Atorvastatin can be increased when it is combined with Tipranavir.
Telithromycin The serum concentration of Atorvastatin can be increased when it is combined with Telithromycin.
Ketoconazole The serum concentration of Atorvastatin can be increased when it is combined with Ketoconazole.
Isavuconazole The metabolism of Atorvastatin can be decreased when combined with Isavuconazole.
Abiraterone The metabolism of Atorvastatin can be decreased when combined with Abiraterone.
Dabrafenib The metabolism of Atorvastatin can be decreased when combined with Dabrafenib.
Etoposide The metabolism of Atorvastatin can be decreased when combined with Etoposide.
Azelastine The metabolism of Atorvastatin can be decreased when combined with Azelastine.
Aldesleukin The metabolism of Atorvastatin can be decreased when combined with Aldesleukin.
Octreotide The metabolism of Atorvastatin can be decreased when combined with Octreotide.
Fluvoxamine The metabolism of Atorvastatin can be decreased when combined with Fluvoxamine.
Citalopram The metabolism of Atorvastatin can be decreased when combined with Citalopram.
Nelfinavir The metabolism of Atorvastatin can be decreased when combined with Nelfinavir.
Indinavir The metabolism of Atorvastatin can be decreased when combined with Indinavir.
Lovastatin The risk or severity of myopathy, rhabdomyolysis, and myoglobinuria can be increased when Lovastatin is combined with Atorvastatin.
Ziprasidone The metabolism of Atorvastatin can be decreased when combined with Ziprasidone.
Cabergoline The metabolism of Atorvastatin can be decreased when combined with Cabergoline.
Diethylstilbestrol The metabolism of Atorvastatin can be decreased when combined with Diethylstilbestrol.
Isradipine The metabolism of Atorvastatin can be decreased when combined with Isradipine.
Valproic acid The metabolism of Atorvastatin can be decreased when combined with Valproic acid.
Acetaminophen The metabolism of Atorvastatin can be decreased when combined with Acetaminophen.
Dihydroergotamine The metabolism of Atorvastatin can be decreased when combined with Dihydroergotamine.
Methadone The metabolism of Atorvastatin can be decreased when combined with Methadone.
Terfenadine The metabolism of Atorvastatin can be decreased when combined with Terfenadine.
Methylergometrine The metabolism of Atorvastatin can be decreased when combined with Methylergometrine.
Mefloquine The metabolism of Atorvastatin can be decreased when combined with Mefloquine.
Clozapine The metabolism of Atorvastatin can be decreased when combined with Clozapine.
Mirtazapine The metabolism of Atorvastatin can be decreased when combined with Mirtazapine.
Sorafenib The metabolism of Atorvastatin can be decreased when combined with Sorafenib.
Nitric Oxide The metabolism of Atorvastatin can be decreased when combined with Nitric Oxide.
Cerivastatin The metabolism of Atorvastatin can be decreased when combined with Cerivastatin.
Teniposide The metabolism of Atorvastatin can be decreased when combined with Teniposide.
Chloramphenicol The metabolism of Atorvastatin can be decreased when combined with Chloramphenicol.
Lansoprazole The metabolism of Atorvastatin can be decreased when combined with Lansoprazole.
Raloxifene The metabolism of Atorvastatin can be decreased when combined with Raloxifene.
Cimetidine The metabolism of Atorvastatin can be decreased when combined with Cimetidine.
Haloperidol The metabolism of Atorvastatin can be decreased when combined with Haloperidol.
Ritonavir The metabolism of Atorvastatin can be decreased when combined with Ritonavir.
Ciprofloxacin The metabolism of Atorvastatin can be decreased when combined with Ciprofloxacin.
Zafirlukast The metabolism of Atorvastatin can be decreased when combined with Zafirlukast.
Vinblastine The metabolism of Atorvastatin can be decreased when combined with Vinblastine.
Fluticasone propionate The metabolism of Atorvastatin can be decreased when combined with Fluticasone propionate.
Thiopental The metabolism of Atorvastatin can be decreased when combined with Thiopental.
Imatinib The metabolism of Atorvastatin can be decreased when combined with Imatinib.
Nicardipine The metabolism of Atorvastatin can be decreased when combined with Nicardipine.
Astemizole The metabolism of Atorvastatin can be decreased when combined with Astemizole.
Dextropropoxyphene The metabolism of Atorvastatin can be decreased when combined with Dextropropoxyphene.
Epinephrine The metabolism of Atorvastatin can be decreased when combined with Epinephrine.
Aprepitant The metabolism of Atorvastatin can be decreased when combined with Aprepitant.
Tamoxifen The metabolism of Atorvastatin can be decreased when combined with Tamoxifen.
Daunorubicin The metabolism of Atorvastatin can be decreased when combined with Daunorubicin.
Ergotamine The metabolism of Atorvastatin can be decreased when combined with Ergotamine.
Amprenavir The metabolism of Atorvastatin can be decreased when combined with Amprenavir.
Delavirdine The metabolism of Atorvastatin can be decreased when combined with Delavirdine.
Paroxetine The metabolism of Atorvastatin can be decreased when combined with Paroxetine.
Tranylcypromine The metabolism of Atorvastatin can be decreased when combined with Tranylcypromine.
Tetracycline The metabolism of Atorvastatin can be decreased when combined with Tetracycline.

Target Protein

3-hydroxy-3-methylglutaryl-coenzyme A reductase HMGCR
Dipeptidyl peptidase 4 DPP4
Aryl hydrocarbon receptor AHR
Histone deacetylase 2 HDAC2
Nuclear receptor subfamily 1 group I member 3 NR1I3

Referensi & Sumber

Artikel (PubMed)
  • PMID: 28658127
    Qiu S, Zhuo W, Sun C, Su Z, Yan A, Shen L: Effects of atorvastatin on chronic subdural hematoma: A systematic review. Medicine (Baltimore). 2017 Jun;96(26):e7290. doi: 10.1097/MD.0000000000007290.
  • PMID: 28613530
    McIver LA, Siddique MS: Atorvastatin .
  • PMID: 25591572
    Ye YC, Zhao XL, Zhang SY: Use of atorvastatin in lipid disorders and cardiovascular disease in Chinese patients. Chin Med J (Engl). 2015 Jan 20;128(2):259-66. doi: 10.4103/0366-6999.149226.
  • PMID: 11298482
    Ray SK, Rege NN: Atorvastatin: in the management of hyperlipidaemia. J Postgrad Med. 2000 Jul-Sep;46(3):242-3.
  • PMID: 14531725
    Lennernas H: Clinical pharmacokinetics of atorvastatin. Clin Pharmacokinet. 2003;42(13):1141-60.
  • PMID: 12686673
    Lins RL, Matthys KE, Verpooten GA, Peeters PC, Dratwa M, Stolear JC, Lameire NH: Pharmacokinetics of atorvastatin and its metabolites after single and multiple dosing in hypercholesterolaemic haemodialysis patients. Nephrol Dial Transplant. 2003 May;18(5):967-76.
  • PMID: 26648697
    Zhao W, Zhao SP: Different effects of statins on induction of diabetes mellitus: an experimental study. Drug Des Devel Ther. 2015 Nov 24;9:6211-23. doi: 10.2147/DDDT.S87979. eCollection 2015.
  • PMID: 10503952
    Moghadasian MH: Clinical pharmacology of 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors. Life Sci. 1999;65(13):1329-37. doi: 10.1016/s0024-3205(99)00199-x.
Menampilkan 8 dari 33 artikel.
Textbook
  • ISBN: 978-0-470-26096-8
    Corey E., Czako B. and Kurti L. (2007). Molecules and medicine. John Wiley & Sons, Inc.
  • ISBN: 978-1-78262-050-1
    Kumar R. and Bandichhor R. (2018). Hazardous reagent substitution. A pharmaceutical perspective. The Royal Society of Chemistry.

Contoh Produk & Brand

Produk: 1226 • International brands: 18
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Menampilkan 8 dari 1226 produk.
International Brands
  • Atogal — Ingers (Czech Republic)
  • Cardyl — Pfizer (Spain)
  • Faboxim — Fabop (Argentina)
  • Hipolixan — Pasteur (Chile)
  • Lipotropic — Drugtech (Chile)
  • Liprimar — Pfizer (Hungary, Ukraine), Goedecke (Russia)
  • Lowden — Saval (Chile)
  • Normalip — Quesada (Argentina)
  • Sincol — Indeco (Argentina)
  • Sortis — Pfizer (Austria, Czech Republic, Germany, Hungary, Poland, Portugal, Switzerland), Godecke (Germany), Parke, Davis (Germany)

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