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This medicine is known as cyclobenzaprine.

If you are a consumer or patient please visit this version. It is freely soluble in water and alcohol, sparingly soluble in isopropanol, and insoluble in hydrocarbon solvents. If aqueous solutions are made alkaline, the free base separates. Cyclobenzaprine HCl is designated chemically as 3- 5H -dibenzo[ a,d ]cycloheptenylidene - N , N -dimethylpropanamine hydrochloride, and has the following structural formula:. Cyclobenzaprine Hydrochloride Tablets, USP are supplied as 5 mg and 10 mg tablets for oral administration.

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If you are a consumer or patient please visit this version. It is freely soluble in water and alcohol, sparingly soluble in isopropanol, and insoluble in hydrocarbon solvents. If aqueous solutions are made alkaline, the free base separates. Cyclobenzaprine HCl is designated chemically as 3- 5H-dibenzo[a,d]cycloheptenylidene -N,N-dimethylpropanamine hydrochloride, and has the following structural formula:. Cyclobenzaprine Hydrochloride Tablets, USP are supplied as 5 mg and 10 mg tablets for oral administration. Cyclobenzaprine HCl relieves skeletal muscle spasm of local origin without interfering with muscle function. It is ineffective in muscle spasm due to central nervous system disease. Cyclobenzaprine reduced or abolished skeletal muscle hyperactivity in several animal models. Animal studies indicate that cyclobenzaprine does not act at the neuromuscular junction or directly on skeletal muscle. Such studies show that cyclobenzaprine acts primarily within the central nervous system at brain stem as opposed to spinal cord levels, although its action on the latter may contribute to its overall skeletal muscle relaxant activity.

Hypersensitivity to any component of this product.

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This medicine is known as cyclobenzaprine. Blood tests, imaging tests and more are used to diagnose musculoskeletal disorders. Here's an overview of the tests and procedures used.

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These are not indicative of addiction. Respiratory: Dyspnea. Cyclobenzaprine Hydrochloride Tablets, USP are supplied as 5 mg and 10 mg tablets for oral administration. Analysis of the data from controlled studies shows that cyclobenzaprine produces clinical improvement whether or not sedation occurs. Concomitant administration of cyclobenzaprine hydrochloride tablets and naproxen or diflunisal was well tolerated with no reported unexpected adverse effects. The adverse reactions reported most frequently with cyclobenzaprine hydrochloride were drowsiness, dry mouth and dizziness. Cyclobenzaprine did not affect the onset, incidence or distribution of neoplasia in an week study in the mouse or in a week study in the rat. Based on the findings, cyclobenzaprine hydrochloride tablets should be used with caution in subjects with mild hepatic impairment starting with the 5 mg dose and titrating slowly upward. At oral doses of up to 10 times the human dose, cyclobenzaprine did not adversely affect the reproductive performance or fertility of male or female rats. For most patients, the recommended dose of cyclobenzaprine hydrochloride tablets is 5 mg three times a day. Reproduction studies have been performed in rats, mice and rabbits at doses up to 20 times the human dose, and have revealed no evidence of impaired fertility or harm to the fetus due to cyclobenzaprine. Special Senses: Ageusia; tinnitus. The incidence of drowsiness, the most frequent adverse reaction, was similar with both drugs.

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Nervous System and Psychiatric: Decreased or increased libido; abnormal gait; delusions; aggressive behavior; paranoia; peripheral neuropathy; Bell's palsy; alteration in EEG patterns; extrapyramidal symptoms. Clinical Studies with Cyclobenzaprine Hydrochloride Tablets 10 mg. Cyclobenzaprine hydrochloride tablets have not been found effective in the treatment of spasticity associated with cerebral or spinal cord disease, or in children with cerebral palsy. Product Information. Other reactions, reported rarely for cyclobenzaprine hydrochloride under circumstances where a causal relationship could not be established or reported for other tricyclic drugs, are listed to serve as alerting information to physicians:. It is not known whether this drug is excreted in human milk. In such patients cyclobenzaprine should be initiated with a 5 mg dose and titrated slowly upward. A similar effect was observed with cyclobenzaprine hydrochloride tablets 10 mg all endpoints. Pharmacological studies in animals showed a similarity between the effects of cyclobenzaprine and the structurally related tricyclic antidepressants, including reserpine antagonism, norepinephrine potentiation, potent peripheral and central anticholinergic effects, and sedation. Musculoskeletal: Myalgia. Improvement is manifested by relief of muscle spasm and its associated signs and symptoms, namely, pain, tenderness, limitation of motion, and restriction in activities of daily living. Cyclobenzaprine Hydrochloride Tablets, USP are supplied as 5 mg and 10 mg tablets for oral administration. We anticipate reposting the images once we are able identify and filter out images that do not match the information provided in the drug labels.