Peringatan Keamanan

Oral acute (LD50): 4000 mg/kg (mouse), 2210 mg/kg (rat) MSDS.

Overdose

Symptoms of overdose include confusion, drowsiness, blurred vision, tachycardia, nausea, diaphoresis, flushing, headache, and dry mouth.

Carcinogenesis and mutagenesis

In 24-month studies in rats, a dose-related significant increase in gastric carcinoid tumors and ECL cell hyperplasia was seen in male and female animals. Carcinoid tumors have also been found in rats treated with a fundectomy or long-term treatment with other proton pump inhibitors, or high doses of H2-receptor antagonists FDA label.

Omeprazole showed positive clastogenic effects in an in vitro human lymphocyte chromosomal aberration study, in one of two in vivo mouse micronucleus tests, and in an in vivo bone marrow cell chromosomal aberration test. Omeprazole tested negative in the in vitro Ames test, an in vitro mouse lymphoma cell forward mutation assay, and an in vivo rat liver DNA damage assay FDA label.

The use in breastfeeding

Limited data indicate that omeprazole may be present in human milk. There is currently no information on the effects of omeprazole on the breastfed infant or production of milk. The benefits of breastfeeding should be considered along with the level of need for omeprazole and any potential adverse effects on the breastfed infant from omeprazole FDA label.

Effects on fertility

Effects of omeprazole at oral doses up to 138 mg/kg/day in rats (about 34 times an oral human dose) was found to have no impact on fertility and reproductive performance FDA label.

Omeprazole

DB00338

small molecule approved investigational vet_approved

Deskripsi

Originally approved by the FDA in 1989, omeprazole is a proton-pump inhibitor, used to treat gastric acid-related disorders. These disorders may include gastroesophageal reflux disease (GERD), peptic ulcer disease, and other diseases characterized by the oversecretion of gastric acid. This drug was the first clinical useful drug in its class, and its approval was followed by the formulation of many other proton pump inhibitor drugs A174232. Omeprazole is generally effective and well-tolerated, promoting its popular use in children and adults FDA label.

Struktur Molekul 2D

Berat 345.416
Wujud solid

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

Profil Farmakokinetik

Waktu Paruh (Half-Life) 0.5-1 hour (healthy subjects, delayed-release capsule) [FDA label] Approximately 3 hours (hepatic impairment) [FDA label]
Volume Distribusi Approximately 0.3 L/kg, corresponding to the volume of extracellular water [A175156].
Klirens (Clearance) Healthy subject (delayed release capsule), total body clearance 500 - 600 mL/min [FDA label] Geriatric plasma clearance: 250 mL/min [FDA label] Hepatic impairment plasma clearance: 70 mL/min [FDA label]

Absorpsi

Omeprazole delayed-release capsules contain an enteric-coated granule formulation of omeprazole (because omeprazole is acid-labile), so that absorption of omeprazole begins only after the granules exit the stomach FDA label. Absorption of omeprazole occurs rapidly, with peak plasma concentrations of omeprazole achieved within 0.5-3.5 hours FDA label. Absolute bioavailability (compared with intravenous administration) is approximately 30-40% at doses of 20-40 mg, largely due to pre-systemic metabolism. The bioavailability of omeprazole increases slightly upon repeated administration of omeprazole delayed-release capsules FDA label.

Metabolisme

Omeprazole is heavily metabolized in the liver by the cytochrome P450 (CYP) enzyme system. The main part of its metabolism depends on the polymorphically expressed CYP2C19, which is responsible for the formation of hydroxyomeprazole, the major metabolite found in plasma. The remaining part depends on CYP3A4, responsible for the formation of omeprazole sulphone FDA label.

Rute Eliminasi

After a single dose oral dose of a buffered solution of omeprazole, negligible (if any) amounts of unchanged drug were excreted in urine. Most of the dose (about 77%) was eliminated in urine as at least six different metabolites. Two metabolites were identified as hydroxyomeprazole and the corresponding carboxylic acid. The remainder of the dose was found in the feces. This suggests significant biliary excretion of omeprazole metabolites. Three metabolites have been identified in the plasma, the sulfide and sulfone derivatives of omeprazole, and hydroxyomeprazole. These metabolites possess minimal or no antisecretory activity FDA label.

Farmakogenomik

2 Varian
CYP2C19 (rs4244285)

Patients with this genotype have reduced metabolism of omeprazole.

CYP2C19 (rs4986893)

Patients with this genotype have reduced metabolism of omeprazole.

Interaksi Makanan

1 Data
  • 1. Take before a meal. Allow 30-60 minutes before a meal.

Interaksi Obat

290 Data
Cyclosporine The serum concentration of Cyclosporine can be increased when it is combined with Omeprazole.
Cilostazol The serum concentration of Cilostazol can be increased when it is combined with Omeprazole.
Dabrafenib The serum concentration of Omeprazole can be decreased when it is combined with Dabrafenib.
Amphetamine Omeprazole can cause an increase in the absorption of Amphetamine resulting in an increased serum concentration and potentially a worsening of adverse effects.
Atazanavir Omeprazole can cause a decrease in the absorption of Atazanavir resulting in a reduced serum concentration and potentially a decrease in efficacy.
Bosutinib Omeprazole can cause a decrease in the absorption of Bosutinib resulting in a reduced serum concentration and potentially a decrease in efficacy.
Cefditoren The serum concentration of Cefditoren can be decreased when it is combined with Omeprazole.
Dabigatran etexilate Omeprazole can cause a decrease in the absorption of Dabigatran etexilate resulting in a reduced serum concentration and potentially a decrease in efficacy.
Dasatinib Omeprazole can cause a decrease in the absorption of Dasatinib resulting in a reduced serum concentration and potentially a decrease in efficacy.
Delavirdine Omeprazole can cause a decrease in the absorption of Delavirdine resulting in a reduced serum concentration and potentially a decrease in efficacy.
Dextroamphetamine Omeprazole can cause an increase in the absorption of Dextroamphetamine resulting in an increased serum concentration and potentially a worsening of adverse effects.
Erlotinib Omeprazole can cause a decrease in the absorption of Erlotinib resulting in a reduced serum concentration and potentially a decrease in efficacy.
Fluconazole The metabolism of Omeprazole can be decreased when combined with Fluconazole.
Gefitinib Omeprazole can cause a decrease in the absorption of Gefitinib resulting in a reduced serum concentration and potentially a decrease in efficacy.
Indinavir Omeprazole can cause a decrease in the absorption of Indinavir resulting in a reduced serum concentration and potentially a decrease in efficacy.
Itraconazole Omeprazole can cause a decrease in the absorption of Itraconazole resulting in a reduced serum concentration and potentially a decrease in efficacy.
Ledipasvir Omeprazole can cause a decrease in the absorption of Ledipasvir resulting in a reduced serum concentration and potentially a decrease in efficacy.
Methylphenidate Omeprazole can cause an increase in the absorption of Methylphenidate resulting in an increased serum concentration and potentially a worsening of adverse effects.
Dexmethylphenidate Omeprazole can cause an increase in the absorption of Dexmethylphenidate resulting in an increased serum concentration and potentially a worsening of adverse effects.
Nelfinavir The serum concentration of Nelfinavir can be decreased when it is combined with Omeprazole.
Nilotinib The serum concentration of Nilotinib can be decreased when it is combined with Omeprazole.
Pazopanib Omeprazole can cause a decrease in the absorption of Pazopanib resulting in a reduced serum concentration and potentially a decrease in efficacy.
Posaconazole Omeprazole can cause a decrease in the absorption of Posaconazole resulting in a reduced serum concentration and potentially a decrease in efficacy.
Raltegravir Omeprazole can cause an increase in the absorption of Raltegravir resulting in an increased serum concentration and potentially a worsening of adverse effects.
Rilpivirine Omeprazole can cause a decrease in the absorption of Rilpivirine resulting in a reduced serum concentration and potentially a decrease in efficacy.
Riociguat Omeprazole can cause a decrease in the absorption of Riociguat resulting in a reduced serum concentration and potentially a decrease in efficacy.
Risedronic acid Omeprazole can cause an increase in the absorption of Risedronic acid resulting in an increased serum concentration and potentially a worsening of adverse effects.
Saquinavir The serum concentration of Saquinavir can be increased when it is combined with Omeprazole.
Tipranavir The metabolism of Omeprazole can be increased when combined with Tipranavir.
Voriconazole The serum concentration of Omeprazole can be increased when it is combined with Voriconazole.
Luliconazole The serum concentration of Omeprazole can be increased when it is combined with Luliconazole.
Phenytoin The serum concentration of Phenytoin can be increased when it is combined with Omeprazole.
Fosphenytoin The serum concentration of Fosphenytoin can be increased when it is combined with Omeprazole.
Levothyroxine Omeprazole can cause a decrease in the absorption of Levothyroxine resulting in a reduced serum concentration and potentially a decrease in efficacy.
Acenocoumarol The metabolism of Acenocoumarol can be decreased when combined with Omeprazole.
(R)-warfarin The metabolism of (R)-warfarin can be decreased when combined with Omeprazole.
(S)-Warfarin The metabolism of (S)-Warfarin can be decreased when combined with Omeprazole.
Bisacodyl The therapeutic efficacy of Bisacodyl can be decreased when used in combination with Omeprazole.
Captopril Omeprazole can cause a decrease in the absorption of Captopril resulting in a reduced serum concentration and potentially a decrease in efficacy.
Cefuroxime The serum concentration of Cefuroxime can be decreased when it is combined with Omeprazole.
Memantine Omeprazole may decrease the excretion rate of Memantine which could result in a higher serum level.
Sulpiride The therapeutic efficacy of Sulpiride can be increased when used in combination with Omeprazole.
Mesalazine Omeprazole can cause a decrease in the absorption of Mesalazine resulting in a reduced serum concentration and potentially a decrease in efficacy.
Mycophenolic acid Omeprazole can cause a decrease in the absorption of Mycophenolic acid resulting in a reduced serum concentration and potentially a decrease in efficacy.
Tolevamer The therapeutic efficacy of Tolevamer can be decreased when used in combination with Omeprazole.
Alendronic acid The therapeutic efficacy of Alendronic acid can be decreased when used in combination with Omeprazole.
Ibandronate The therapeutic efficacy of Ibandronate can be decreased when used in combination with Omeprazole.
Clodronic acid The therapeutic efficacy of Clodronic acid can be decreased when used in combination with Omeprazole.
Etidronic acid The therapeutic efficacy of Etidronic acid can be decreased when used in combination with Omeprazole.
Tiludronic acid The therapeutic efficacy of Tiludronic acid can be decreased when used in combination with Omeprazole.
Incadronic acid The therapeutic efficacy of Incadronic acid can be decreased when used in combination with Omeprazole.
Cysteamine The bioavailability of Cysteamine can be decreased when combined with Omeprazole.
Ketoconazole Omeprazole can cause a decrease in the absorption of Ketoconazole resulting in a reduced serum concentration and potentially a decrease in efficacy.
Lumacaftor The serum concentration of Omeprazole can be decreased when it is combined with Lumacaftor.
Tacrolimus The metabolism of Tacrolimus can be decreased when combined with Omeprazole.
Methenamine The therapeutic efficacy of Methenamine can be decreased when used in combination with Omeprazole.
Fluvoxamine The metabolism of Omeprazole can be decreased when combined with Fluvoxamine.
Ticlopidine The metabolism of Omeprazole can be decreased when combined with Ticlopidine.
Chloramphenicol The metabolism of Omeprazole can be decreased when combined with Chloramphenicol.
Lansoprazole The metabolism of Omeprazole can be decreased when combined with Lansoprazole.
Fluoxetine The metabolism of Omeprazole can be decreased when combined with Fluoxetine.
Isoniazid The metabolism of Omeprazole can be decreased when combined with Isoniazid.
Zafirlukast The metabolism of Omeprazole can be decreased when combined with Zafirlukast.
Eslicarbazepine acetate The metabolism of Omeprazole can be decreased when combined with Eslicarbazepine acetate.
Felbamate The metabolism of Omeprazole can be decreased when combined with Felbamate.
Medical Cannabis The metabolism of Medical Cannabis can be decreased when combined with Omeprazole.
Imatinib The metabolism of Imatinib can be decreased when combined with Omeprazole.
Valproic acid The metabolism of Omeprazole can be decreased when combined with Valproic acid.
Nicardipine The metabolism of Omeprazole can be decreased when combined with Nicardipine.
Miconazole The metabolism of Omeprazole can be decreased when combined with Miconazole.
Gemfibrozil The metabolism of Omeprazole can be decreased when combined with Gemfibrozil.
Topiroxostat The metabolism of Omeprazole can be decreased when combined with Topiroxostat.
Quinine The metabolism of Quinine can be decreased when combined with Omeprazole.
Apalutamide The serum concentration of Omeprazole can be increased when it is combined with Apalutamide.
Testosterone The metabolism of Testosterone can be decreased when combined with Omeprazole.
Mycophenolate mofetil Omeprazole can cause a decrease in the absorption of Mycophenolate mofetil resulting in a reduced serum concentration and potentially a decrease in efficacy.
Glyburide The metabolism of Glyburide can be decreased when combined with Omeprazole.
Apixaban The metabolism of Apixaban can be decreased when combined with Omeprazole.
Rucaparib The metabolism of Omeprazole can be decreased when combined with Rucaparib.
Selumetinib The metabolism of Selumetinib can be decreased when combined with Omeprazole.
Gestodene The metabolism of Omeprazole can be decreased when combined with Gestodene.
Lynestrenol The metabolism of Lynestrenol can be decreased when combined with Omeprazole.
Albendazole The metabolism of Albendazole can be decreased when combined with Omeprazole.
Doxazosin The metabolism of Doxazosin can be decreased when combined with Omeprazole.
Fenofibrate The metabolism of Omeprazole can be decreased when combined with Fenofibrate.
Isavuconazole The metabolism of Omeprazole can be decreased when combined with Isavuconazole.
Bortezomib The metabolism of Omeprazole can be decreased when combined with Bortezomib.
Tamoxifen The metabolism of Tamoxifen can be decreased when combined with Omeprazole.
Cyclophosphamide The metabolism of Cyclophosphamide can be decreased when combined with Omeprazole.
Trabectedin The metabolism of Trabectedin can be decreased when combined with Omeprazole.
Carbamazepine The metabolism of Omeprazole can be decreased when combined with Carbamazepine.
Teniposide The metabolism of Teniposide can be decreased when combined with Omeprazole.
Enasidenib The metabolism of Enasidenib can be decreased when combined with Omeprazole.
Axitinib The metabolism of Axitinib can be decreased when combined with Omeprazole.
Clomipramine The metabolism of Omeprazole can be decreased when combined with Clomipramine.
Nilutamide The metabolism of Nilutamide can be decreased when combined with Omeprazole.
Nilvadipine The metabolism of Omeprazole can be decreased when combined with Nilvadipine.
Ethinylestradiol The metabolism of Omeprazole can be decreased when combined with Ethinylestradiol.
Quercetin The metabolism of Omeprazole can be decreased when combined with Quercetin.
Methylene blue The metabolism of Methylene blue can be decreased when combined with Omeprazole.

Target Protein

Potassium-transporting ATPase alpha chain 1 ATP4A
Potassium-transporting ATPase subunit beta ATP4B
Aryl hydrocarbon receptor AHR

Referensi & Sumber

Synthesis reference: Arne E. Brandstrom, Bo R. Lamm, "Processes for the preparation of omeprazole and intermediates therefore." U.S. Patent US4620008, issued October, 1982.
Artikel (PubMed)
  • PMID: 17190895
    Yang YX, Lewis JD, Epstein S, Metz DC: Long-term proton pump inhibitor therapy and risk of hip fracture. JAMA. 2006 Dec 27;296(24):2947-53.
  • PMID: 16259581
    Castell D: Review of immediate-release omeprazole for the treatment of gastric acid-related disorders. Expert Opin Pharmacother. 2005 Nov;6(14):2501-10. doi: 10.1517/14656566.6.14.2501 .
  • PMID: 29547594
    Higuera-de-la-Tijera F: Efficacy of omeprazole/sodium bicarbonate treatment in gastroesophageal reflux disease: a systematic review. Medwave. 2018 Mar 14;18(2):e7179. doi: 10.5867/medwave.2018.02.7179.
  • PMID: 10665250
    Welage LS, Berardi RR: Evaluation of omeprazole, lansoprazole, pantoprazole, and rabeprazole in the treatment of acid-related diseases. J Am Pharm Assoc (Wash). 2000 Jan-Feb;40(1):52-62; quiz 121-3.
  • PMID: 2690330
    Cederberg C, Andersson T, Skanberg I: Omeprazole: pharmacokinetics and metabolism in man. Scand J Gastroenterol Suppl. 1989;166:33-40; discussion 41-2.
  • PMID: 27840364
    Strand DS, Kim D, Peura DA: 25 Years of Proton Pump Inhibitors: A Comprehensive Review. Gut Liver. 2017 Jan 15;11(1):27-37. doi: 10.5009/gnl15502.
  • PMID: 1718683
    McTavish D, Buckley MM, Heel RC: Omeprazole. An updated review of its pharmacology and therapeutic use in acid-related disorders. Drugs. 1991 Jul;42(1):138-70. doi: 10.2165/00003495-199142010-00008.
  • PMID: 9777317
    Langtry HD, Wilde MI: Omeprazole. A review of its use in Helicobacter pylori infection, gastro-oesophageal reflux disease and peptic ulcers induced by nonsteroidal anti-inflammatory drugs. Drugs. 1998 Sep;56(3):447-86. doi: 10.2165/00003495-199856030-00012.
Menampilkan 8 dari 15 artikel.

Contoh Produk & Brand

Produk: 810 • International brands: 37
Produk
  • 24 Hr Omeprazole
    Tablet, delayed release • 20 mg/1 • Oral • US • OTC • Approved
  • Ach-omeprazole
    Tablet, delayed release • 20 mg • Oral • Canada • Generic • Approved
  • Acid Reducer
    Capsule, delayed release • 20 mg/1 • Oral • US • Generic • OTC • Approved
  • Acid Reducer
    Tablet, delayed release • 20 mg/1 • Oral • US • Generic • OTC • Approved
  • Acid Reducer
    Tablet, delayed release • 20 mg/1 • Oral • US • Generic • OTC • Approved
  • Acid Reducer
    Tablet, delayed release • 20 mg/1 • Oral • US • Generic • OTC • Approved
  • Acid Reducer
    Tablet, delayed release • 20 mg/1 • Oral • US • Generic • OTC • Approved
  • Acid Reducer
    Tablet, delayed release • 20 mg/1 • Oral • US • Generic • OTC • Approved
Menampilkan 8 dari 810 produk.
International Brands
  • Antra
  • Audazol
  • Belmazol
  • Ceprandal
  • Danlox
  • Desec
  • Elgam
  • Emeproton
  • Gasec
  • Gastrimut

Sekuens Gen/Protein (FASTA)

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