দেশ: মার্কিন যুক্তরাষ্ট্র
ভাষা: ইংরেজি
সূত্র: NLM (National Library of Medicine)
FLUNIXIN MEGLUMINE (UNII: 8Y3JK0JW3U) (FLUNIXIN - UNII:356IB1O400), PHENOL (UNII: 339NCG44TV) (PHENOL - UNII:339NCG44TV)
Agri Laboratories, Ltd
FLUNIXIN MEGLUMINE
FLUNIXIN MEGLUMINE 50 mg in 1 mL
INTRAMUSCULAR
PRESCRIPTION
Horse : Flu-Nix is recommended for the alleviation of inflammation and pain associated with musculoskeletal disorders in the horse. It is also recommended for the alleviation of visceral pain associated with colic in the horse. Cattle : Flu-Nix is indicated for the control of pyrexia associated with bovine respiratory disease, endotoxemia and acute bovine mastitis. Flu-Nix is also indicated for the control of inflammation in endotoxemia. Horse : There are no known contraindications to this drug when used as directed. Intra-arterial injection should be avoided. Horses inadvertently injected intra-arterial can show adverse reactions. Signs can be ataxia, incoordination, hyperventilation, hysteria, and muscle weakness. Signs are transient and disappear without antidotal medication within a few minutes. Do not use in horses showing hypersensitivity to flunixin meglumine. Cattle : There are no known contraindications to this drug in cattle when used as directed. Do not use in animals showing hypersensi
Flu-Nix, 50 mg/mL, is available in 100 mL and 250 mL multi-dose vials.
Abbreviated New Animal Drug Application
FLU-NIX - FLUNIXIN MEGLUMINE INJECTION, SOLUTION AGRI LABORATORIES, LTD ---------- FLU-NIX (FLUNIXIN MEGLUMINE) INJECTABLE SOLUTION 50 MG/ML ANADA 200-061, APPROVED BY FDA VETERINARY For Intravenous or Intramuscular Use in Horses and for Intravenous Use in Beef and Dairy Cattle. Not for Use in Dry Dairy Cows and Veal Calves. Read accompanying directions for use. CAUTION: Federal law restricts this drug to use by or on the order of a licensed veterinarian. DES CRIPTION Each milliliter of Flu-Nix contains flunixin meglumine equivalent to 50 mg flunixin, 0.1 mg edetate disodium, 2.5 mg sodium formaldehyde sulfoxylate, 4.0 mg diethanolamine, 207.2 mg propylene glycol, 5.0 mg phenol as preservative, hydrochloric acid, water for injection q.s. PHARMACOLOGY Flunixin meglumine is a potent, non-narcotic, non-steroidal, analgesic agent with anti-inflammatory and anti-pyretic activity. It is significantly more potent than pentazocine, meperidine and codeine as an analgesic in the rat yeast paw test. HORSE: Flunixin is four times as potent on a mg/per mg basis as phenylbutazone as measured by the reduction of lameness and swelling in the horse. Plasma half-life in horse serum is 1.6 hours following a single dose of 1.1 mg/kg. Measurable amounts are detectable in horse plasma at 8 hours post injection. CATTLE: Flunixin meglumine is a weak acid (pKa=5.82) which exhibits a high degree of plasma protein binding (approximately 99%). However, free (unbound) drug appears to readily partition into body tissues (V predictions range from 297 to 782 mL/kg. Total body water is approximately equal to 570 ml/kg). In cattle, elimination occurs primarily through biliary elimination occurs primarily through biliary excretion. This may, at least in part, explain the presence of multiple peaks in the blood concentration/time profile following IV administration. In healthy cattle, total body clearance has been reported to range from 90 to 151 mL/kg/hr. These studies also report a large discrepancy between the volume of distribution at a steady সম্পূর্ণ নথি পড়ুন