संयुक्त राज्य - अंग्रेज़ी - NLM (National Library of Medicine)

akorn - lidocaine hydrochloride anhydrous (unii: ec2cnf7xfp) (lidocaine - unii:98pi200987) - akten® is indicated for ocular surface anesthesia during ophthalmologic procedures. none. reproduction studies for lidocaine have been performed in both rats and rabbits. there was no evidence of harm to the fetus at subcutaneous doses up to 50 mg/kg lidocaine (more than 800 fold greater than the human dose on a body weight basis) in the rat model. there are, however, no adequate and well controlled studies in pregnant women. because animal reproduction studies are not always predictive of human response, this drug should be used in pregnancy only if clearly needed. lidocaine is secreted in human milk. the clinical significance of this observation is unknown. although no systemic exposure is expected with administration of akten® , caution should be exercised when akten® is administered to a nursing woman. safety and efficacy in pediatric patients have been extrapolated from studies in older subjects and studies in pediatric patients using different formulations of lidocaine. no overall clinical differences

संयुक्त राज्य - अंग्रेज़ी - NLM (National Library of Medicine)

akorn - loteprednol etabonate (unii: yeh1ez96k6) (loteprednol - unii:z8cbu6kr16) - loteprednol etabonate is indicated for the treatment of steroid responsive inflammatory conditions of the palpebral and bulbar conjunctiva, cornea and anterior segment of the globe such as allergic conjunctivitis, acne rosacea, superficial punctate keratitis, herpes zoster keratitis, iritis, cyclitis, selected infective conjunctivitides, when the inherent hazard of steroid use is accepted to obtain an advisable diminution in edema and inflammation. loteprednol etabonate is less effective than prednisolone acetate 1% in two 28-day controlled clinical studies in acute anterior uveitis, where 72% of patients treated with loteprednol etabonate experienced resolution of anterior chamber cells, compared to 87% of patients treated with prednisolone acetate 1%. the incidence of patients with clinically significant increases in iop (≥10 mmhg) was 1% with loteprednol etabonate and 6% with prednisolone acetate 1%. loteprednol etabonate should not be used in patients who require a more potent corticosteroid for this indi

संयुक्त राज्य - अंग्रेज़ी - NLM (National Library of Medicine)

henry schein animal health - ketamine hydrochloride (unii: o18yuo0i83) (ketamine - unii:690g0d6v8h) - ketathesia™ (ketamine hydrochloride injection, usp) may be used in cats for restraint or as the sole anesthetic agent for diagnostic or minor, brief, surgical procedures that do not require skeletal muscle relaxation. it may be used in subhuman primates for restraint. ketamine hydrochloride is contraindicated in cats and subhuman primates suffering from renal or hepatic insufficiency. ketamine hydrochloride is detoxified by the liver and excreted by the kidneys; therefore, any preexistent hepatic or renal pathology or impairment of function can be expected to result in prolonged anesthesia; related fatalities have been reported.

संयुक्त राज्य - अंग्रेज़ी - NLM (National Library of Medicine)

akorn - polyvinyl alcohol, unspecified (unii: 532b59j990) (polyvinyl alcohol, unspecified - unii:532b59j990) - eye lubricant for use as a lubricant to prevent further irritation or to relieve dryness of the eye(s).

संयुक्त राज्य - अंग्रेज़ी - NLM (National Library of Medicine)

remedyrepack inc. - buprenorphine hydrochloride (unii: 56w8mw3en1) (buprenorphine - unii:40d3scr4gz) - buprenorphine sublingual tablets is indicated for the treatment of opioid dependence and is preferred for induction. buprenorphine sublingual tablets should be used as part of a complete treatment plan to include counseling and psychosocial support. buprenorphine sublingual tablets is contraindicated in patients with a history of hypersensitivity to buprenorphine, as serious adverse reactions, including anaphylactic shock, have been reported [see warnings and precautions ( 5.9)] . risk summary the data on use of buprenorphine, the active ingredient in buprenorphine sublingual tablets, in pregnancy, are limited; however, these data do not indicate an increased risk of major malformations specifically due to buprenorphine exposure. there are limited data from randomized clinical trials in women maintained on buprenorphine that were not designed appropriately to assess the risk of major malformations [see data] . observational studies have reported on congenital malformations among

संयुक्त राज्य - अंग्रेज़ी - NLM (National Library of Medicine)

remedyrepack inc. - levetiracetam (unii: 44yrr34555) (levetiracetam - unii:44yrr34555) - levetiracetam oral solution is indicated for the treatment of partial-onset seizures in patients 1 month of age and older. levetiracetam oral solution is indicated as adjunctive therapy in the treatment of myoclonic seizures in adults and adolescents 12 years of age and older with juvenile myoclonic epilepsy. levetiracetam oral solution is indicated as adjunctive therapy in the treatment of primary generalized tonic-clonic seizures in patients 6 years of age and older with idiopathic generalized epilepsy. levetiracetam is contraindicated in patients with a hypersensitivity to levetiracetam. reactions have included anaphylaxis and angioedema [see warnings and precautions (5.4) ]. levetiracetam blood levels may decrease during pregnancy [see warnings and precautions (5.10) ]. pregnancy category c there are no adequate and controlled studies in pregnant women. in animal studies, levetiracetam produced evidence of developmental toxicity, including teratogenic effects, at doses similar

संयुक्त राज्य - अंग्रेज़ी - NLM (National Library of Medicine)

butler animal health supply, llc dba covetrus north america - ketamine hydrochloride (unii: o18yuo0i83) (ketamine - unii:690g0d6v8h) - ketamine hcl injection, usp may be used in cats for restraint or as the sole anesthetic agent for diagnostic or minor, brief, surgical procedure that do not require skeletal muscle relaxation. it may be used in subhuman primates for restraint. ketamine hydrochloride is contraindicated in cats and subhuman primates suffering from renal or hepatic insufficiency. ketamine hydrochloride is detoxified by the liver and excreted by the kidneys; therefore, any preexistent hepatic or renal pathology or impairment of function can be expected to result in prolonged anesthesia; related fatalities have been reported.

संयुक्त राज्य - अंग्रेज़ी - NLM (National Library of Medicine)

butler animal health supply, llc dba covetrus north america - mineral oil (unii: t5l8t28fgp) (mineral oil - unii:t5l8t28fgp), petrolatum (unii: 4t6h12bn9u) (petrolatum - unii:4t6h12bn9u) - eye lubricant eye lubricant for use as a lubricant to prevent further irritation or to relieve dryness of the eye(s).

संयुक्त राज्य - अंग्रेज़ी - NLM (National Library of Medicine)

butler animal health supply, llc dba covetrus north america - butorphanol tartrate (unii: 2l7i72ruhn) (butorphanol - unii:qv897jc36d) - butorphanol tartrate is indicated for the relief of pain associated with colic in adult horses and yearlings. clinical studies in the horse have shown that butorphanol tartrate alleviates abdominal pain, associated with torsion, impaction, intussusception, spasmodic and tympanic colic, and postpartum pain.

संयुक्त राज्य - अंग्रेज़ी - NLM (National Library of Medicine)

aspen veterinary resources - neomycin sulfate (unii: 057y626693) (neomycin - unii:i16qd7x297), polymyxin b sulfate (unii: 19371312d4) (polymyxin b - unii:j2vz07j96k), bacitracin zinc (unii: 89y4m234es) (bacitracin - unii:58h6rwo52i) - this product is indicated for the treatment of superficial bacterial infections of the eyelid and conjunctiva of dogs and cats when due to organisms susceptible to one or more of the antibiotics contained in the ointment. laboratory tests should be conducted including in vitro culturing and susceptibility tests on samples collected prior to treatment.