tilmicosin and Tachycardia

tilmicosin has been researched along with Tachycardia* in 3 studies

Other Studies

3 other study(ies) available for tilmicosin and Tachycardia

ArticleYear
Analysis of reports of human exposure to Micotil 300 (tilmicosin injection).
    Journal of the American Veterinary Medical Association, 2006, Dec-01, Volume: 229, Issue:11

    To identify clinical signs associated with and outcome of human exposure to Micotil 300 (tilmicosin injection).. Retrospective case series.. Reports of 3,168 human exposures to Micotil 300.. Reports of human exposure to Micotil 300 submitted to the Elanco Animal Health Pharmacovigilance Unit between March 1992 and March 2005 were reviewed.. At least 1 clinical sign was described in 1,404 (44%) reports, whereas the remaining 1,764 (56%) exposures were presumably asymptomatic. Eighty percent of exposures involved males; mean age was 38 years. Sixty-one percent of exposures were a result of accidental injection, with injection site pain, bleeding, swelling, or inflammation being the most common signs, followed by nausea, tachycardia, dizziness, anxiety, an abnormal taste, headache, lightheadedness, limb pain, paresthesia, chest pain, and soreness. Only 156 (5%) reports involved serious adverse effects (ie, tachycardia, bradycardia, hypertension, hypotension, heart disorder, chest pain, tachypnea, or death). There were reports of 13 deaths following tilmicosin exposure, but only 2 of those deaths were related to accidental exposure. Time to onset of clinical signs was < or = 60 minutes in 63 of the 156 (40%) reports involving serious adverse effects.. Results suggest that the overall risk of accidental human exposure to tilmicosin resulting in serious adverse effects is low (approx 2 people for every 1 million doses administered). Nevertheless, safe handling and proper use should be emphasized.

    Topics: Accidents, Occupational; Adult; Anti-Bacterial Agents; Chest Pain; Female; Humans; Macrolides; Male; Needlestick Injuries; Occupational Exposure; Retrospective Studies; Tachycardia; Tylosin; Veterinary Drugs

2006
Accidental veterinary antibiotic injection into a farm worker.
    Tennessee medicine : journal of the Tennessee Medical Association, 1999, Volume: 92, Issue:9

    A 29-year-old white male farm worker accidentally injected tilmicosin, a bovine antibiotic, into his finger. He developed temporary pulmonary, gastrointestinal, and neuromuscular symptomatology and a more persistent subjective asthenia.

    Topics: Accidents, Occupational; Adult; Angina Pectoris; Animal Husbandry; Animals; Anti-Bacterial Agents; Ataxia; Cattle; Cattle Diseases; Humans; Injections, Intradermal; Macrolides; Male; Paralysis; Respiratory Tract Diseases; Tachycardia; Tylosin

1999
Cardiovascular effects of the macrolide antibiotic tilmicosin, administered alone and in combination with propranolol or dobutamine, in conscious unrestrained dogs.
    Journal of veterinary pharmacology and therapeutics, 1996, Volume: 19, Issue:3

    Tilmicosin(TM), a macrolide antibiotic and active ingredient in formulated Micotil 300 (Eli Lilly and Co., Indianapolis, IN, USA), is the active ingredient in a formulated animal product used for the treatment of respiratory tract infections in cattle. Owing to the concern of governmental regulatory agencies over the possibility of an accidental injection of the antibiotic to a livestock handler, the cardiovascular effects of sub lethal doses of TM were evaluated in conscious mixed-breed dogs. Left ventricular function, systemic arterial blood pressure, and heart rate (HR) responses to TM alone and in combination with propranolol(P) or dobutamine HCl(DOB) were evaluated. Dogs were instrumented with indwelling micromanometers implanted in the left ventricular chamber and in the thoracic aorta. Cardiovascular variables were recorded, and the peak value of the first derivative of left ventricular pressure (dp/dt(max)) was used as an index of left ventricular inotropic state. Six treatments were randomly assigned to each of the six dogs using a Latin square design. The six treatments were vehicle, TM alone (2.5 mg/kg of body weight), TM immediately followed by P, and TM immediately followed by 1 of 3 dosages of DOB infused for approximately 45 min. Additionally, doses of TM alone (0.25, 1.0, 2.5, and 5.0 mg/kg) were administered to complete a dose-response curve. TM caused dose dependent decreases in (dp/dt(max)) and aortic pulse pressure. HR increased dose-dependently. Left ventricular end-diastolic pressure increased at the 2.5 and 5.0 mg/kg dosages. Left ventricular systolic pressure was reduced dose-dependently at the 2.5 and 5.0 mg/kg dosages. Treatment with P exacerbated the negative inotropic effect and the decrease in left ventricular systolic pressure, but did not attenuate the tachycardia associated with TM treatment. DOB attenuated the changes in ventricular inotropic state in a dose-dependent manner. DOB infusion also restored left ventricular systolic pressure at dosages of 3 or 10 micrograms/min/kg. Our data indicate that toxic doses of TM may have a negative inotropic effect in conscious dogs. HR increased in a dose-dependent manner and was not the result of beta 1-receptor stimulation. DOB reversed some, but not all, of the effects caused by TM administration.

    Topics: Adrenergic beta-Agonists; Adrenergic beta-Antagonists; Analysis of Variance; Animals; Anti-Bacterial Agents; Blood Pressure; Calibration; Dobutamine; Dogs; Dose-Response Relationship, Drug; Drug Evaluation; Drug Interactions; Female; Heart Rate; Injections, Intravenous; Linear Models; Macrolides; Male; Myocardial Contraction; Propranolol; Tachycardia; Tylosin; Ventricular Function, Left

1996