IMMITICIDE- melarsomine dihydrochloride and water kit Ameerika Ühendriigid - inglise - NLM (National Library of Medicine)

immiticide- melarsomine dihydrochloride and water kit

boehringer ingelheim animal health usa inc. - melarsomine dihydrochloride (unii: 9cva716q71) (melarsomine - unii:374gj0s41a) - immiticide sterile power is indicated for the treatment of stabilized class 1a , 2b , and 3c heartworm disease caused by immature (4 month-old, stage l5 ) to mature adult infections of dirofilaria immitis in dogs. heartworm disease classification : the following parameters were used to classify the dogs in the clinical field trials for immiticide. other parameters may be considered. as a general rule, conservative treatment should be employed since heartworm disease is serious and potentially fatal. if there is evidence of a high worm burden, patients should be categorized as class 3. a class 1: patients in this category are characterized as having asymptomatic to mild heartworm disease. no radiographic signs or signs of anemia are evident. patients with mild disease may have subjective signs such as a general loss of condition, fatigue on exercise, or occasional cough; however, no objective radiographic or other abnormal laboratory parameters will be present. b class 2: patients in this category are characterized as having moderate heartworm disease. radiographic signs or signs of anemia [packed cell volume (pcv) less than 30% but greater than 20%, or other hematologic parameters below normal] are evident. mild proteinuria (2+) may be present. radiographic signs may include right ventricular enlargement, slight pulmonary artery enlargement, or circumscribed perivascular densities plus mixed alveolar/interstitial lesions. patients may be free of subjective clinical signs or may have a general loss of condition, fatigue on exercise, or occasional cough. if necessary, patients should be stabilized prior to treatment. c class 3: patients in this category are characterized as having severe heartworm disease. these patients have a guarded prognosis. subjective signs of disease may include cardiac cachexia (wasting), constant fatigue, persistent cough, dyspnea, or other signs associated with right heart failure such as ascites and/or jugular pulse. radiographic signs may include right ventricular enlargement or right ventricular plus right atrial enlargement, severe pulmonary artery enlargement, circumscribed to chronic mixed patterns and diffuse patterns of pulmonary densities or radiographic signs of thromboembolism. signs of significant anemia (pcv <20% or other hematologic abnormalities) may be present. proteinuria (>2+) may be present. patients may have only moderate clinical signs and significant laboratory or radiographic alterations or they may have significant clinical signs with only moderate laboratory and radiographic signs and be categorized as class 3. patients in class 3 should be stabilized prior to treatment and then administered the alternate dosing regime (see precautions and dosage and administration ). immiticide is contraindicated in dogs with very severe (class 4) heartworm disease. patients in this category have caval syndrome (d. immitis present in the venae cavae and right atrium).

SYNCHSURE- cloprostenol sodium injection, solution Ameerika Ühendriigid - inglise - NLM (National Library of Medicine)

synchsure- cloprostenol sodium injection, solution

boehringer ingelheim animal health usa inc. - cloprostenol sodium (unii: 886sav9675) (cloprostenol - unii:4208238832) - indications: for intramuscular use to induce luteolysis in beef and dairy cattle. the luteolytic action of synchsure can be utilized to manipulate the estrous cycle to better fit certain management practices, to terminate pregnancies resulting from mismatings, and to treat certain conditions associated with prolonged luteal function. contraindications: synchsure should not be administered to a pregnant animal whose calf is not to be aborted.

SENVELGO- velagliflozin solution Ameerika Ühendriigid - inglise - NLM (National Library of Medicine)

senvelgo- velagliflozin solution

boehringer ingelheim animal health usa inc. - velagliflozin proline (unii: eqe2p2t77i) (velagliflozin - unii:fv2yu8sl0p) - do not use senvelgo in cats with diabetes mellitus who have previously been treated with insulin, who are receiving insulin, or in cats with insulin-dependent diabetes mellitus. the use of senvelgo in cats with insulin-dependent diabetes mellitus, or the withdrawal of insulin and initiation of senvelgo, is associated with an increased risk of diabetic ketoacidosis or euglycemic diabetic ketoacidosis and death.

DISAL- furosemide injection Ameerika Ühendriigid - inglise - NLM (National Library of Medicine)

disal- furosemide injection

boehringer ingelheim animal health usa inc. - furosemide (unii: 7lxu5n7zo5) (furosemide - unii:7lxu5n7zo5) - furosemide 50 mg in 1 ml - dogs and horses: disal injection is an effective diuretic-saluretic for use in the treatment of acute noninflammatory tissue edema in dogs and horses, and for use in the treatment of edema (pulmonary congestion, ascites) associated with cardiac insufficiency in the dog. in cases of edema involving cardiac insufficiency, the continued use of heart stimulants such as digitalis or its glycosides is indicated. the rationale for efficacious use of diuretic therapy in either dogs or horses is determined by the clinical pathology producing the edema. animal reproductive studies have shown that furosemide may cause fetal abnormality and the drug is contraindicated in pregnant bitches, mares and stallions at stud. furosemide is contraindicated in anuria, furosemide hypersensitivity, hepatic coma, or during electrolytic imbalances. monitor serum electrolytes, bun and co2 frequently. monitor serum potassium levels and watch for signs of hypocalcemia. corticosteroids cause an additive potassium-depletion effect.

PROMACE- acepromazine maleate injection Ameerika Ühendriigid - inglise - NLM (National Library of Medicine)

promace- acepromazine maleate injection

boehringer ingelheim animal health usa inc. - acepromazine maleate (unii: 37862hp2om) (acepromazine - unii:54ej303f0r) - acepromazine maleate 10 mg in 1 ml - dogs and cats: promace injectable can be used as an aid in controlling intractable animals during examination, treatment, grooming, x-ray and minor surgical procedures; to alleviate itching as a result of skin irritation; as an antiemetic to control vomiting associated with motion sickness. promace injectable is particularly useful as a preanesthetic agent (1) to enhance and prolong the effects of barbiturates, thus reducing the requirements for general anesthesia; (2) as an adjunct to surgery under local anesthesia. horses: promace injectable can be used as an aid in controlling fractious animals during examination, treatment, loading and transportation. particularly useful when used in conjunction with local anesthesia for firing, castration, neurectomy, removal of skin tumors, ocular surgery and applying casts. phenothiazines may potentiate the toxicity of organophosphates and the activity of procaine hydrochloride. therefore, do not use promace injectable to control tremors associated with organic phosp

EPRINEX POUR-ON FOR BEEF AND DAIRY CATTLE- eprinomectin solution Ameerika Ühendriigid - inglise - NLM (National Library of Medicine)

eprinex pour-on for beef and dairy cattle- eprinomectin solution

boehringer ingelheim animal health usa inc. - eprinomectin (unii: 75kp30fd8o) (eprinomectin - unii:75kp30fd8o) - eprinex (eprinomectin) pour-on is indicated for the treatment and control of gastrointestinal roundworms (including inhibited ostertagia ostertagi ), lungworms, grubs, sucking and biting lice, chorioptic and sarcoptic mange mites, and horn flies in beef and dairy cattle of all ages, including lactating dairy cattle. applied at the recommended dose volume of 1 ml/10 kg (22 lb) body weight, to achieve a dose level of 500 mcg eprinomectin/kg body weight, eprinex pour-on is indicated for the effective treatment and control of the following parasites. gastrointestinal roundworms   haemonchus placei (adults and l4)   ostertagia ostertagi (including inhibited l4) (adults and l4)   trichostrongylus axei (adults and l4)   trichostrongylus colubriformis (adults and l4)   trichostrongylus longispicularis (adults only)   cooperia oncophora (adults and l4)   cooperia punctata (adults and l4)   cooperia surnabada (adults and l4)   nematodirus helvetianus (adults and l4)   oesophagostomum radiatum (adults and l4)   bunostomum phlebotomum (adults and l4)   strongyloides papillosus (adults only)   trichuris spp. (adults only) lungworms   dictyocaulus viviparus (adults and l4) cattle grubs (all parasitic stages)   hypoderma lineatum, hypoderma bovis lice   damalinia bovis, linognathus vituli, haematopinus   eurysternus, solenopotes capillatus mange mites   chorioptes bovis, sarcoptes scabiei horn flies   haematobia irritans eprinex (eprinomectin) pour-on for beef and dairy cattle has been proved to effectively control infections and to protect cattle from re-infection with dictyocaulus viviparus for 21 days after treatment and haematobia irritans for 7 days after treatment. varying weather conditions, including rainfall, do not affect the efficacy of eprinex pour-on. for best results eprinex pour-on should be applied to all cattle in the herd. cattle introduced to the herd later should be treated prior to introduction. consult your veterinarian or an entomologist for the most effective timing of applications for the control of external parasites. chorioptic mange: in clinical studies evaluating the efficacy of eprinex pour-on against chorioptic mange mites, mites were not recovered from skin scrapings taken 8 weeks after treatment; however, chronic skin lesions were still present on some animals. horn flies: for optimal control of horn flies, as eprinex pour-on provides 7 days of persistent activity against horn flies, the product should be used as part of an integrated control program utilizing other control methods to provide extended control.

LONGRANGE- eprinomectin injection, solution Ameerika Ühendriigid - inglise - NLM (National Library of Medicine)

longrange- eprinomectin injection, solution

boehringer ingelheim animal health usa inc. - eprinomectin (unii: 75kp30fd8o) (eprinomectin - unii:75kp30fd8o) - 5% sterile solution extended-release injectable for subcutaneous use parasiticide for cattle on pasture for the treatment and control of internal and external parasites of cattle on pasture with persistent effectiveness not for use in female dairy cattle 20 months of age or older, including dry dairy cows. not for use in calves to be processed for veal. not for use in breeding bulls, or in calves less than 3 months of age. not for use in cattle managed in feedlots or under intensive rotational grazing. caution: federal law restricts this drug to use by or on the order of a licensed veterinarian. longrange, when administered at the recommended dose volume of 1 ml per 110 lb (50 kg) body weight, is effective in the treatment and control of the following internal and external parasites of cattle: bunostomum phlebotomum – adults and l4 dictyocaulus viviparus – adults cooperia oncophora – adults and l4 cooperia punctata – adults and l4 cooperia surnabada – adults and l4 grubs haemonchus placei – adults hypoderma bovis oesophagostomum radiatum – adults ostertagia lyrata – adults mites ostertagia ostertagi – adults, l4 , and inhibited l4 sarcoptes scabiei var. bovis trichostrongylus axei – adults and l4 trichostrongylus colubriformis – adults persistent activity longrange has been proven to effectively protect cattle from reinfection with the following parasites for the indicated amounts of time following treatment: gastrointestinal roundworms   bunostomum phlebotomum 150 days   cooperia oncophora 100 days   cooperia punctata 100 days   haemonchus placei 120 days   oesophagostomum radiatum 120 days   ostertagia lyrata 120 days   ostertagia ostertagi 120 days   trichostrongylus axei 100 days lungworms   dictyocaulus viviparus 150 days

PROMACE- acepromazine maleate tablet Ameerika Ühendriigid - inglise - NLM (National Library of Medicine)

promace- acepromazine maleate tablet

boehringer ingelheim animal health usa inc. - acepromazine maleate (unii: 37862hp2om) (acepromazine - unii:54ej303f0r) - as an aid in tranquilization and as a preanesthetic agent in dogs. promace tablets can be used as an aid in controlling intractable animals during examination, treatment, grooming, x-ray and minor surgical procedures. phenothiazines may potentiate the toxicity of organophosphates. therefore, do not use acepromazine maleate to control tremors associated with organic phosphate poisoning. do not use in conjunction with organophosphorus vermifuges or ectoparasiticides, including flea collars. do not use with procaine hydrochloride.

PROMACE- acepromazine maleate tablet Ameerika Ühendriigid - inglise - NLM (National Library of Medicine)

promace- acepromazine maleate tablet

boehringer ingelheim animal health usa inc. - acepromazine maleate (unii: 37862hp2om) (acepromazine - unii:54ej303f0r) - as an aid in tranquilization and as a preanesthetic agent in dogs. promace tablets can be used as an aid in controlling intractable animals during examination, treatment, grooming, x-ray and minor surgical procedures. phenothiazines may potentiate the toxicity of organophosphates. therefore, do not use acepromazine maleate to control tremors associated with organic phosphate poisoning. do not use in conjunction with organophosphorus vermifuges or ectoparasiticides, including flea collars. do not use with procaine hydrochloride.

VETALOG- triamcinolone acetonide tablet Ameerika Ühendriigid - inglise - NLM (National Library of Medicine)

vetalog- triamcinolone acetonide tablet

boehringer ingelheim animal health usa inc. - triamcinolone acetonide (unii: f446c597ka) (triamcinolone acetonide - unii:f446c597ka) - triamcinolone acetonide is a highly potent glucocorticoid effective in the treatment of inflammation and related disorders in dogs and cats. it is indicated in the management and treatment of acute arthritis and allergic and dermatologic disorders. do not use in viral infections. except for emergency therapy, do not use in animals with tuberculosis, chronic nephritis, cushingoid syndrome and peptic ulcers. existence of congestive heart failure, diabetes and osteoporosis are relative contraindications.