Austrália - angličtina - Department of Health (Therapeutic Goods Administration)

panpharma australia pty ltd - erythromycin lactobionate, quantity: 1.49 g (equivalent: erythromycin, qty 1 g) - injection, powder for - excipient ingredients: - oral erythromycin is not considered to be the antibiotic of choice in severely ill patients.,erythromycin panpharma (sterile erythromycin lactobionate) is indicated in the treatment of infections caused by susceptible strains of the designated organisms in the diseases listed below when oral administration is not possible or when the severity of the infection requires immediate high serum levels of erythromycin. intravenous therapy should be replaced by oral administration at the appropriate time.,? upper respiratory tract infections caused by streptococcus pyogenes (group a beta-haemolytic streptococci); streptococcus pneumoniae (diplococcus pneumoniae); haemophilus influenzae (many strains of h. influenzae are not susceptible to the erythromycin concentrations ordinarily achieved).,? lower respiratory tract infections caused by streptococcus pyogenes (group a beta-haemolytic streptococci); streptococcus pneumoniae (diplococcus pneumoniae).,? respiratory tract infections due to mycoplasma pneumoniae.,? skin and skin structure infections caused by streptococcus pyogenes and staphylococcus aureus (resistant staphylococci may emerge during treatment).,? diphtheria - as an adjunct to diphtheria antitoxin in infections due to corynebacterium diphtheriae to prevent establishment of carriers and to eradicate the organism in carriers.,? acute pelvic inflammatory disease caused by neisseria gonorrhoeae: erythromycin panpharma (sterile erythromycin lactobionate) followed by erythromycin stearate, base or ethyl succinate orally, as an alternative drug in treatment of acute pelvic inflammatory disease caused by n. gonorrhoeae in female patients with a history of sensitivity to penicillin.,? before treatment of gonorrhoea, patients who are suspected of also having syphilis should have microscopic examination for t. pallidum (by immuno-fluorescence or dark field) before receiving erythromycin and monthly serologic tests for a minimum of 4 months thereafter.,? legionnaires' disease caused by legionella pneumophila. although no controlled clinical efficacy studies have been conducted, in vitro and limited preliminary clinical data suggest that erythromycin may be effective in treating legionnaires' disease.

Malta - angličtina - Medicines Authority

hospira uk limited horizon, honey lane, hurley, maidenhead sl6 6rj, united kingdom - remifentanil - powder for solution for infusion or injection - remifentanil 1 mg - anesthetics

Malta - angličtina - Medicines Authority

hospira uk limited horizon, honey lane, hurley, maidenhead sl6 6rj, united kingdom - remifentanil - powder for solution for infusion or injection - remifentanil 2 mg - anesthetics

Malta - angličtina - Medicines Authority

hospira uk limited horizon, honey lane, hurley, maidenhead sl6 6rj, united kingdom - remifentanil - powder for solution for infusion or injection - remifentanil 5 mg - anesthetics

Malta - angličtina - Medicines Authority

fresenius kabi limited cestrian court, eastgate way, manor park, runcorn, cheshire wa7 1nt, united kingdom - remifentanil - powder for concentrate for solution for infusion or injection - remifentanil 1 mg - anesthetics

Malta - angličtina - Medicines Authority

fresenius kabi limited cestrian court, eastgate way, manor park, runcorn, cheshire wa7 1nt, united kingdom - remifentanil - powder for concentrate for solution for infusion or injection - remifentanil 2 mg - anesthetics

Malta - angličtina - Medicines Authority

fresenius kabi limited cestrian court, eastgate way, manor park, runcorn, cheshire wa7 1nt, united kingdom - remifentanil - powder for concentrate for solution for infusion or injection - remifentanil 5 mg - anesthetics

Írsko - angličtina - HPRA (Health Products Regulatory Authority)

actavis group ptc ehf - remifentanil - powder for concentrate for solution for injection/infusion - 2 milligram(s) - opioid anesthetics; remifentanil

Írsko - angličtina - HPRA (Health Products Regulatory Authority)

actavis group ptc ehf - remifentanil - powder for concentrate for solution for injection/infusion - 5 milligram(s) - opioid anesthetics; remifentanil

Írsko - angličtina - HPRA (Health Products Regulatory Authority)

actavis group ptc ehf - remifentanil - powder for concentrate for solution for injection/infusion - 1 milligram(s) - opioid anesthetics; remifentanil