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Travoprost. Travoprost, sold under the brand name Travatan among others, is a medication used to treat high pressure inside the eye including glaucoma. [ 4] Specifically it is used for open angle glaucoma when other agents are not sufficient. [ 5][ 4] It is used as an eye drop. [ 4] Effects generally occur within two hours.
Trazodone's potent α 1-adrenergic blockade may cause some side effects like orthostatic hypotension and sedation. [114] Conversely, along with 5-HT 2A and H 1 receptor antagonism, it may contribute to its efficacy as a hypnotic. Trazodone lacks any affinity for the muscarinic acetylcholine receptors, so does not produce anticholinergic side ...
Acepromazine. Acepromazine, acetopromazine, or acetylpromazine (commonly known as ACP, Ace, or by the trade names Atravet or Acezine 2, number depending on mg/ml dose) is a phenothiazine derivative antipsychotic drug. It was used in humans during the 1950s as an antipsychotic, [4] but is now almost exclusively used on animals as a sedative and ...
The post Trazodone for Dogs: Uses, Dosage, & Side Effects appeared first on DogTime. ... The typical starting dose ranges from 1 to 2 mg per pound of body weight, given every 8 to 24 hours. This ...
The recommended dosage is 2 mg of Adequan per pound of body weight, given as an intramuscular injection. Typically, the treatment plan starts with a series of injections spread over a specific period.
For heartworm prevention, the typical dose is relatively low, at 0.0015 – 0.003 mg per pound of body weight, administered orally once a month. For the treatment of mange, doses can be higher and ...
Maropitant. Maropitant ( INN; [ 2] brand name: Cerenia, used as maropitant citrate ( USAN ), is a neurokinin-1 (NK 1) receptor antagonist developed by Zoetis specifically for the treatment of motion sickness and vomiting in dogs. It was approved by the FDA in 2007, for use in dogs [ 3][ 4] and in 2012, for cats.
Atipamezole. Atipamezole , sold under the brand name Antisedan among others, is a synthetic α 2 adrenergic receptor antagonist used for the reversal of the sedative and analgesic effects of dexmedetomidine and medetomidine in dogs. Its reversal effect works by competing with the sedative for α 2 -adrenergic receptors and displacing them.