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Linevex

Linevex

linezolid

Manufacturer:

Anfarm Hellas

Distributor:

Sannovex
Concise Prescribing Info
Contents
Linezolid
Indications/Uses
Community acquired pneumonia & nosocomial pneumonia when known or suspected to be caused by susceptible gm +ve bacteria; complicated skin & soft tissue infections only when microbiological testing has established that the infection is known to be caused by susceptible gm +ve bacteria.
Dosage/Direction for Use
IV infusion Administer over a period of 30-120 min. Adult 600 mg bid. Duration of treatment: 10-14 consecutive days. Max: 28 days.
Contraindications
Hypersensitivity. Patients w/ uncontrolled HTN, phaeochromocytoma, carcinoid, thyrotoxicosis, bipolar depression, schizoaffective disorder, acute confusional states. Not be used in patients taking any medicinal product which inhibits MAOIs A or B (eg, phenelzine, isocarboxazid, selegiline, moclobemide) or w/in 2 wk of taking any such medicinal product. Patients taking SSRIs, TCAs, serotonin 5-HT1 receptor agonists (triptans), directly & indirectly acting sympathomimetic agents (including adrenergic bronchodilators, pseudoephedrine & phenylpropanolamine), vasopressive agents (eg, epinephrine, norepinephrine), dopaminergic agents (eg, dopamine, dobutamine), pethidine or buspirone.
Special Precautions
Reports of myelosuppression (including anaemia, leucopenia, pancytopenia & thrombocytopenia); antibiotic-associated diarrhoea & colitis, including pseudomembranous colitis & Clostridium difficile-associated diarrhoea; lactic acidosis; peripheral & optic neuropathy; convulsions. Monitor CBC wkly (including Hb levels, platelets, & total & differentiated leucocyte counts). Advise patients to report symptoms of visual impairment. Inhibits mitochondrial protein synthesis which may result in adverse events eg, lactic acidosis, anaemia & neuropathy. Not recommended for use in patients w/ underlying conditions &/or on concomitant medications which might put them at risk from MAO inhibition. Increased risk of neuropathies when used in patients currently taking or who have recently taken antimycobacterial medications for TB. May occasionally result in an overgrowth of non-susceptible organisms. Patients should be advised against consuming large amounts of tyramine rich foods. Consider glucose & Na content in patients w/ DM or other conditions associated w/ glucose intolerance, & patients on controlled Na diet, respectively. Potential for dizziness or symptoms of visual impairment while receiving treatment; advise patients not to drive or operate machinery if any of these symptoms occur. Patients w/ severe renal insufficiency, those undergoing dialysis; patients w/ severe hepatic insufficiency. No experience of administration to patients undergoing continuous ambulatory peritoneal dialysis or alternative treatments for renal failure (other than haemodialysis). Possible effects on male reproductive system are not known. Not to be used during pregnancy unless clearly necessary. Breast-feeding should be discontinued prior to & throughout administration. Not recommended in childn & adolescents (<18 yr). Elderly patients may be at greater risk of experiencing blood dyscrasias than younger patients.
Adverse Reactions
Lactic acidosis, anaemia, & optic & peripheral neuropathy.
Drug Interactions
Risk of serotonin syndrome w/ other MAOIs. Increased BP w/ pseudoephedrine or phenylpropanolamine; drugs w/ vasopressive action, including dopaminergic agents. Possible pressor w/ excessive amounts of food & beverages w/ high tyramine content (eg, mature cheese, yeast extr, undistilled alcoholic beverages & fermented soya bean products eg, soy sauce). Decreased Cmax & AUC w/ rifampicin. Reduced mean max INR w/ warfarin.
MIMS Class
Other Antibiotics
ATC Classification
J01XX08 - linezolid ; Belongs to the class of other antibacterials. Used in the systemic treatment of infections.
Presentation/Packing
Form
Linevex soln for IV infusion 2 mg/mL
Packing/Price
300 mL x 1's
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