FLUNIXIJECT- flunixin meglumine injection, solution United States - English - NLM (National Library of Medicine)

flunixiject- flunixin meglumine injection, solution

henry schein animal health - flunixin meglumine (unii: 8y3jk0jw3u) (flunixin - unii:356ib1o400) - flunixin meglumine 50 mg in 1 ml - indications horse: flunixiject™ injectable solution 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: flunixiject™ injectable solution is indicated for the control of pyrexia associated with bovine respiratory disease, endotoxemia and acute bovine mastitis. flunixiject™ injectable solution is also indicated for the control of inflammation in endotoxemia. contraindications horse: there are no known contraindications to this drug when used as directed. intra-arterial injection should be avoided. horses inadvertently injected intra-arterially 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: nsaids inhibit production of

FLUNAZINE- flunixin meglumine injection, solution United States - English - NLM (National Library of Medicine)

flunazine- flunixin meglumine injection, solution

bimeda, inc. - flunixin meglumine (unii: 8y3jk0jw3u) (flunixin - unii:356ib1o400) - flunixin meglumine 50 mg in 1 ml - indications horse :  flunazine® injectable solution 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 :  flunazine® injectable solution is indicated for the control of pyrexia associated with bovine respiratory disease, endotoxemia and acute bovine mastitis.  flunazine® injectable solution is also indicated for the control of inflammation in endotoxemia. contraindications horse :  there are no known contraindications to this drug when used as directed.  intra-arterial injection should be avoided.  horses inadvertently injected intra-arterially 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 :  nsaids inhibit production of prostaglandins which are important in signaling the initiation of parturition. the use of flunixin can delay parturition and prolong labor which may increase the risk of stillbirth. do not use flunazine® injectable solution within 48 hours of expected parturition.  do not use in animals showing hypersensitivity to flunixin meglumine.  use judiciously when renal impairment or gastric ulceration are suspected.

FLU-NIX- flunixin meglumine injection, solution United States - English - NLM (National Library of Medicine)

flu-nix- flunixin meglumine injection, solution

agri laboratories, ltd - flunixin meglumine (unii: 8y3jk0jw3u) (flunixin - unii:356ib1o400), phenol (unii: 339ncg44tv) (phenol - unii:339ncg44tv) - flunixin meglumine 50 mg in 1 ml - 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

X - flunixin meglumine powder United States - English - NLM (National Library of Medicine)

x - flunixin meglumine powder

ax pharmaceutical corp - flunixin meglumine (unii: 8y3jk0jw3u) (flunixin meglumine - unii:8y3jk0jw3u) - flunixin meglumine 495 g in 500 g

X - flunixin meglumine powder United States - English - NLM (National Library of Medicine)

x - flunixin meglumine powder

ax pharmaceutical corp - flunixin meglumine (unii: 8y3jk0jw3u) (flunixin meglumine - unii:8y3jk0jw3u) - flunixin meglumine 24750 g in 25000 g

FLUNIXIN MEGLUMINE Australia - English - APVMA (Australian Pesticides and Veterinary Medicines Authority)

flunixin meglumine

neove pharma australia pty limited - flunixin meglumine - unknown - flunixin meglumine benzene active 0.0 - active constituent

Flunixin Meglumine Australia - English - APVMA (Australian Pesticides and Veterinary Medicines Authority)

flunixin meglumine

mavlab pty. ltd. - flunixin meglumine - unknown - flunixin meglumine benzene active 0.0 - active constituent

BANAMINE- flunixin meglumine solution United States - English - NLM (National Library of Medicine)

banamine- flunixin meglumine solution

merck sharp & dohme corp. - flunixin meglumine (unii: 8y3jk0jw3u) (flunixin - unii:356ib1o400) - flunixin 50 mg in 1 ml - indications: banamine transdermal pour-on is indicated for the control of pyrexia associated with bovine respiratory disease and acute bovine mastitis, and the control of pain associated with foot rot in beef cattle 2 months of age and older and dairy cattle. not for use in beef and dairy bulls intended for breeding over 1 year of age, replacement dairy heifers over 20 months of age, dry dairy cows, dairy calves, or veal calves. contraindications: nsaids inhibit production of prostaglandins which are important in signaling the initiation of parturition. the use of flunixin can delay parturition and prolong labor which may increase the risk of stillbirth. do not use banamine transdermal pour-on within 48 hours of expected parturition. do not use in animals showing hypersensitivity to flunixin meglumine.

NEOVE FLUNIXIN MEGLUMINE INJECTION Australia - English - APVMA (Australian Pesticides and Veterinary Medicines Authority)

neove flunixin meglumine injection

neove pharma australia pty limited - flunixin meglumine - parenteral liquid/solution/suspension - flunixin meglumine benzene active 50.0 mg/ml - musculoskeletal system - cattle | dog | horse | pigs | beef | bitch | boar | bos indicus | bos taurus | bovine | buffalo | bull | bullock | calf | castra - analgesic | anti-inflammatory agent | antiprostaglandin | antipyretic | bone soreness | bruising | bursitis | colic | inflammatory rheumatic arthrit | joint disease | ligament sprains | muscle relaxant | muscle soreness | osteoarthritis | platelet activity | rheumatism | sedative | spasmolytic | sprains | strains | tendon sprains | traumatic swelling

Flunixin Injection Ireland - English - HPRA (Health Products Regulatory Authority)

flunixin injection

norbrook laboratories (ireland) limited - flunixin meglumine - solution for injection - 50 milligram(s)/millilitre - flunixin