Amika500 mg/2 ml

Amika 500 mg/2 ml is indicated in the short-term treatment of serious infections due to susceptible strains of Gram-negative bacteria. Amika 500 mg/2 ml is effective in bacterial septicemia (including neonatal sepsis); in serious infections of the respiratory tract, bones and joints, central nervous system (including ... Read moreAmika 500 mg/2 ml is indicated in the short-term treatment of serious infections due to susceptible strains of Gram-negative bacteria. Amika 500 mg/2 ml is effective in bacterial septicemia (including neonatal sepsis); in serious infections of the respiratory tract, bones and joints, central nervous system (including meningitis) and skin and soft tissue; intra-abdominal infections (including peritonitis); and in burns and postoperative infections (including postvascular surgery). Clinical studies have shown Amika 500 mg/2 ml also to be effective in serious complicated and recurrent urinary tract infections due to those organisms.Amika 500 mg/2 ml was effective in infections caused by gentamicin and/or tobramycin-resistant strains of Gram-negative organisms, particularly Proteus rettgeri, Providencia stuartii, Serratia marcescens, and Pseudomonas aeruginosa.Amika 500 mg/2 ml has also been shown to be effective in staphylococci infections and may be considered as initial therapy under certain conditions in the treatment of known or suspected staphylococcal disease such as, severe infections where the causative organism may be either a Gram-negative bacterium or a staphylococcus.

Aminoglycosides

Amika 500 mg/2 ml Sulfate is a semi-synthetic aminoglycoside antibiotic. Amika 500 mg/2 ml is active in vitro against pseudomonas species, Escherichia coli, Proteus species, Providencia species, Klebsiella-Enterobacter species, Acinetobacter species, and Citrobacter freundii. When strains of the above organisms are found to be resistant to other aminoglycosides, including Gentamicin, TobrAmykin and KanAmykin, many are susceptible to Amika 500 mg/2 ml. Amika 500 mg/2 ml sulfate is active in vitro against penicillinase and nonpenicillinase-producing Staphylococcus species including methicillin-resistant strains.

Adults and children: 15 mg/kg/day in two equally-divided doses (equivalent to 500 mg bid in adults). Use of the 100 mg is recommended for children for the accurate measurement of the appropriate dose.Neonates and premature children: An initial loading dose of 10 mg/kg followed by 15 mg/kg/day in two equally divided doses.Elderly: Amika 500 mg/2 ml is excreted by the renal route. Renal function should be assessed whenever possible and dosage adjusted as described under impaired renal function.Life-threatening infections and/or those caused by Pseudomonas: The adult dose may be increased to 500 mg every eight hours but should neither exceed 1.5g/day nor be administered for a period longer than 10 days. A maximum total adult dose of 15g should not be exceeded.Urinary tract infections (other than pseudomonal infections): 7.5mg/kg/day in two equally divided doses (equivalent to 250 mg b.i.d. in adults).Impaired renal function: In patients with impaired renal function, the daily dose should be reduced and/or the intervals between doses increased to avoid accumulation of the drug.

Intramuscular or intravenous administration: For most infections the intramuscular route is preferred, but in life threatening infections, or in patients in whom intramuscular injection route is not feasible the intravenous route may be used.Intraperitoneal use: Amika 500 mg/2 ml may be used as an irrigant after recovery from anesthesia in concentration of 0.25%.

Concurrent administration of Amika 500 mg/2 ml with myorelaxants leads to potentiation of their effects and there is a possibility of cessation of the breathing. The combination with other Aminoglycoside antibiotics should be avoided because of the augmentation of their ototoxic and nephrotoxic effects. Concurrent administration of Amika 500 mg/2 ml with fast acting diuretics increases the risk of ototoxicity in patients with renal failure. Combination with Cephalosporins or Polymixins increases the risk of nephrotoxicity.

Amika 500 mg/2 ml Injection is contraindicated in patients with a known history of hypersensitivity to Amika 500 mg/2 ml, any constituents of the injection.

The adverse effects have been reported with the use of Amika 500 mg/2 ml are tinnitus, vertigo, partial reversible or irreversible deafness, skin rash, drug fever, headache, paraesthesia, nausea and vomiting.

Amika 500 mg/2 ml rapidly crosses the placenta into the foetal circulation and amniotic fluid and there is a potential risk of ototoxicity in the foetus. There is no information available regarding the safety of this drug during breastfeeding.

Since Amika 500 mg/2 ml is present in high concentrations in the renal excretory system, patients should be well hydrated to minimize chemical irritation of the renal tubules. If azotemia increases, treatment should be stopped. Monitoring of renal function during treatment with aminoglycosides is particularly important.

In the event of overdose or toxic reaction, peritoneal dialysis or haemodialysis will aid in the removal of Amika 500 mg/2 ml from the blood.

Keep below 30°C temperature, away from light & moisture. Keep out of the reach of children.

Pediatric Use: Safety and effectiveness of Amika 500 mg/2 ml for injection in children or adolescents under 16 years have not been established

Aminoglycosides

Amika 500 mg/2 ml Sulfate is a semi-synthetic aminoglycoside antibiotic. Amika 500 mg/2 ml is active in vitro against pseudomonas species, Escherichia coli, Proteus species, Providencia species, Klebsiella-Enterobacter species, Acinetobacter species, and Citrobacter freundii. When strains of the above organisms are found to be resistant to other aminoglycosides, including Gentamicin, TobrAmykin and KanAmykin, many are susceptible to Amika 500 mg/2 ml. Amika 500 mg/2 ml sulfate is active in vitro against penicillinase and nonpenicillinase-producing Staphylococcus species including methicillin-resistant strains.

Amika 500 mg/2 ml rapidly crosses the placenta into the foetal circulation and amniotic fluid and there is a potential risk of ototoxicity in the foetus. There is no information available regarding the safety of this drug during breastfeeding.

Pediatric Use: Safety and effectiveness of Amika 500 mg/2 ml for injection in children or adolescents under 16 years have not been established