Telithromycin


Concise Prescribing Info
Indications/Uses
Community-acquired pneumonia.
Dosage/Direction for Use
Adult : PO 800 mg once daily for 7-10 days.
Dosage Details
Oral
Community-acquired pneumonia
Adult: 800 mg once daily for 7-10 days.
Renal Impairment
CrCl Dosage
<30 Alternating daily doses of 800 mg and 400 mg, starting w/ 800 mg.
Administration
May be taken with or without food.
Contraindications
Known hypersensitivity to telithromycin and other macrolides, history of hepatitis and/or jaundice associated w/ macrolide therapy, myasthenia gravis. Patient w/ congenital or known history of QT interval prolongation. Patient w/ renal or hepatic impairment receiving colchicine. Concomitant admin w/ drugs that prolong QT interval and are CYP3A4 substrates, HMG-CoA reductase inhibitors metabolised by CYP3A4 or ergot alkaloid derivatives.
Special Precautions
Patient w/ CHD, cardiac arrhythmias, hypokalaemia or hypomagnesaemia. Hepatic or renal impairment. Pregnancy and lactation.
Adverse Reactions
Diarrhoea, nausea, vomiting, abdominal pain, flatulence, dizziness, headache, vertigo, insomnia, drowsiness, taste and smell disturbances, paraesthesia, eosinophilia, rash, arrhythmias, hypotension, bradycardia, visual disturbances, syncope, angioedema, anaphylaxis, erythema multiforme, muscle cramps.
Potentially Fatal: Hepatotoxicity including fulminant hepatitis, hepatic necrosis and hepatic failure, acute resp failure in patient w/ myasthenia gravis, Clostridium difficile-associated disease (CDAD).
Patient Counseling Information
This drug may cause visual disturbances, confusion or hallucination, if affected, do not drive, operate heavy machinery or engage in other hazardous activities.
MonitoringParameters
Perform LFTs. Closely monitor for signs and symptoms of liver failure (e.g. jaundice, fatigue, nausea, acholic stools) and visual acuity.
Drug Interactions
Additive effect on QT interval prolongation w/ class 1A (e.g. quinidine, procainamide) or class III (e.g. dofetilide) antiarrhythmic agents. Decreased telithromycin concentrations and/or increased anticonvulsant concentrations w/ phenytoin, carbamazepine, phenobarbital. Increased peak plasma concentration and area under the concentration-time curve (AUC) w/ itraconazole and ketoconazole. Decreased peak plasma concentration and AUC w/ rifampicin. Increased AUC of midazolam or levonorgestrel. Increased plasma concentrations of colchicine, digoxin, repaglinide, ciclosporin, sirolimus or tacrolimus. May potentiate effects of oral anticoagulants (e.g. warfarin).
Potentially Fatal: Increased risk of QT interval prolongation and cardiac arrhythmias w/ cisapride, pimozide, astemizole, terfenadine, dronedarone, saquinavir. Increased concentrations of ergot alkaloids (e.g. ergotamine, dihydroergotamine) leading to possible peripheral vasospasm, dysesthesia and acute ergot toxicity. Increased plasma concentrations of CYP3A4 metabolised HMG-CoA reductase inhibitors (e.g. lovastatin, simvastatin, atorvastatin), hence the risk of myopathy and rhabdomyolysis.
Food Interaction
St John's wort may reduce therapeutic effect of telithromycin.
Action
Description: Telithromycin is a semisynthetic ketolide antibiotic that blocks protein synthesis by binding to domains II and V of 23S ribosomal RNA of the 50S ribosome subunit. It may also inhibit the assembly of nascent ribosomal units.
Pharmacokinetics:
Absorption: Rapidly absorbed from the GI tract. Bioavailability: 57%. Time to peak plasma concentration: Approx 1-3 hr.
Distribution: Widely distributed in body fluids and tissues, including the resp tract. Volume of distribution: 2.9 L/kg. Plasma protein binding: 60-70%.
Metabolism: Undergoes hepatic metabolism by CYP3A4 and non-CYP3A4 isoenzymes to 4 major metabolites.
Excretion: Via urine (13% as unchanged drug; remainder as metabolites) and faeces (7%). Elimination half-life: 2-3 hr. Terminal half-life: Approx 10 hr.
Chemical Structure

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Storage
Store at 25°C.
MIMS Class
Disclaimer: This information is independently developed by MIMS based on Telithromycin from various references and is provided for your reference only. Therapeutic uses, prescribing information and product availability may vary between countries. Please refer to MIMS Product Monographs for specific and locally approved prescribing information. Although great effort has been made to ensure content accuracy, MIMS shall not be held responsible or liable for any claims or damages arising from the use or misuse of the information contained herein, its contents or omissions, or otherwise. Copyright © 2020 MIMS. All rights reserved. Powered by MIMS.com
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