Χώρα: Μαλαισία
Γλώσσα: Αγγλικά
Πηγή: NPRA (National Pharmaceutical Regulatory Agency, Bahagian Regulatori Farmasi Negara)
LINCOMYCIN HCL
Y.S.P. INDUSTRIES (M) SDN. BHD.
LINCOMYCIN HCL
100.00 mcg/mL
YUNG SHIN PHARMACEUTICAL IND. CO., LTD.
LINCOMYCIN INJECTION 300MG/ML INGREDIENT(S): Each ml contains: Lincomycin HCl.………………........................300mg/ml (potency) Preservative(s): Each ml contains: Methyl paraben …………………………………………. 1.1mg Propyl paraben …………………………………………. 0.122mg PHARMACOLOGY (SUMMARY OF PHARMACODYNAMICS AND PHARMACOKINETICS): Lincomycin may be bacteriostatic or bactericidal in action, depending on the concentrations of the drug attained at the site of infection and the susceptibility of the infecting organism. Lincomycin appears to inhibit protein synthesis in susceptible organisms by binding to the 50S ribosomal subunit, thereby inhibiting peptide bond formation. Following oral administration, lincomycin is rapidly absorbed from the gut, but only about 30~40% of the total dose is absorbed. Food both decreases the extent and the rate of absorption. Peak serum levels are attained about 2~4 hours after oral dosing. IM administration gives peak levels about double those reached after oral dosing, and peak at about 30 minutes post injection. Lincomycin is distributed into most tissues. Therapeutic levels are achieved in bone, synovial fluid, bile, pleural fluid, peritoneal fluid, skin, and heart muscle. CNS levels may reach 40% of those in the serum if meninges are inflamed. Lincomycin is bound from 57~72% to plasma proteins, depending on the drug’s concentration. The drug crosses the placenta and also can be distributed into milk at concentrations equal to those found in the plasma. Lincomycin is partially metabolised in the liver. Unchanged drug and metabolites are excreted in the urine, feces and bile. The elimination half-life of Lincomycin is reportedly 3~4 hours in small animals, and can be prolonged in patients with renal or hepatic dysfunction. INDICATION(S): 1) For the treatment of infectious forms of arthritis caused by Staphylococci, Streptococci, Erysipelothrix and _Mycoplasma spp._ 2) For the treatment of mycoplasma pneumonia. TARGET SPECIES Swine. Διαβάστε το πλήρες έγγραφο