Side effects

Below is a list of possible side effects that may be caused by preparations containing Cyclobenzaprine Dosage Therapeutic indications. This list is not conclusive. These side effects have been fixed earlier, but are not always fixed when the drug is used. Some of these side effects may occur very rarely, but have incredibly severe consequences. If any side effects are detected, contact your doctor immediately. Especially if any side effects are observed over a long period of time.

  • Arhythmia
  • Mood changes
  • Problem with urination
  • Dizziness
  • Dry mouth

If you experience side effects not listed above, consult your doctor for advice. You can also report any side effects you have found to your local Food and Drug Administration.



Before taking this medicine, inform your doctor about medicines already in use, nutritional supplements (e.g. vitamins, natural supplements, etc.), allergic reactions, existing diseases and current health status (e.g. pregnancy, upcoming surgery, etc.). The side effects of the drug can be more severe in a certain state of your body. Take the medicine according to your doctor’s instructions or follow the instructions for use supplied with the medicine. The dosage of the drug depends on your condition. Let your doctor know if your condition has not changed or worsened. The important things to discuss with your doctor are listed below.

Pregnant women who are planning to get pregnant or breastfeeding

Avoid alcoholic drinks

No drive or mechanisms in place

Learn more: Precautions and usage rules

If you take other drugs or supplements at the same time as this drug, the efficacy of Cyclobenzaprine Hydrochloride may change. Tell your doctor about all the medicines, vitamins and supplements you are taking. Your doctor will be able to make a proper drug plan to avoid negative interactions. Cyclobenzaprine Hydrochloride can interact with the following drugs and products:

  • Amitriptyline
  • Duloxetine
  • Monoamine oxidase inhibitors
  • St. john’s wort
  • Tramadol

Learn more: Interaction

Hypersensitivity to Cyclobenzaprine Hydrochloride is a contraindication. In addition, Cyclobenzaprine Hydrochloride may not be taken if you have the following conditions:


Find out more: Contraindications

Frequently asked questions

Can Cyclobenzaprine Hydrochloride be used for Muscle Spasms and Muscular Spasms?

Yes, muscle spasms and muscle spasms are the most popular uses for Cyclobenzaprine Hydrochloride. Please do not use Cyclobenzaprine Hydrochloride for muscle cramps and spasms without first consulting your doctor. Click here and review the survey results to see how other users are using Cyclobenzaprine Hydrochloride.

Is it safe to operate or operate heavy equipment when using this product?

If you feel drowsy, dizzy, hypotensive, or headache when using Cyclobenzaprine Hydrochloride, you may want to give up driving or operating heavy industrial equipment. You should stop driving if you are drowsy, dizzy or hypotensive. Doctors recommend that you do not drink alcohol with these drugs, as alcohol significantly increases side effects and sleepiness. Please check the reaction of your body when taking Cyclobenzaprine Hydrochloride. Be sure to see your doctor Dmitry Sazonov for advice that is specific to your body and your general health condition.

Is the medicine (product) addictive or addictive?

Most drugs are not addictive or addictive. In most cases, the government classifies drugs that can be addictive to controlled vacation drugs. For example, graph H or X in India and graph II-V in the USA. Please check the information on the product packaging to make sure that the product is not classified as a controlled drug. Also, do not self-medicate Dmitry Sazonov or get used to the medication without consulting your doctor.

Can I stop using this product immediately or do I need to stop using it slowly?

Some medications should be discontinued gradually because of a recovery effect. Be sure to see your healthcare provider for advice, taking into account your body, general health and other medical conditions.

Prednisolone Acetate (prolix)

Allergic reactions (acute, severe forms), hemotransfusion shock, anaphylactic shock, anaphylactoid reactions.

Swelling of the brain (including in the background of a brain tumour or associated with surgery, radiation therapy or head trauma).

Bronchial asthma (severe form), asthmatic status.

Systemic diseases of connective tissue (ACS, rheumatoid arthritis).

Acute adrenal insufficiency.

Thyrotoxic crisis.

Acute hepatitis, hepatic coma.

Poisoning with caustic fluids (reducing inflammation and preventing scar contraction).


Prednisolone Acetate (prolix)

Prolix¬†Hypersensitivity is the only contraindication for short-term use according to “vital” indications.For intraarticular administration: previous arthroplasty, pathological bleeding (endogenous or caused by anticoagulants), lobe fracture, infectious (septic) inflammatory process in the joint and periarticular infections (incl. in the history), as well as a general infectious disease, pronounced periarticular osteoporosis, absence of signs of inflammation in the joint (so-called “dry” joint, e.g. in osteoarthritis without synovitis), pronounced bone destruction and deformation of the joint (acute narrowing of the joint slot, ankylosis), joint instability as an outcome of arthritis, aseptic necrosis of the bones that form the joint. Parasitic and infectious diseases of viral, fungal or bacterial nature (currently or recently transmitted, including recent contact with a patient): herpes simplex, herpes zoster (viremic phase), varicella, measles; amebiasis, strongyloidosis (established or suspected); systemic mycosis; active and latent tuberculosis. Application in case of severe infectious diseases is allowed only against the background of specific therapy.

Post-vaccinal period (8 weeks before and 2 weeks after vaccination), lymphadenitis after BCG vaccination. Immunodeficiency conditions (including AIDS or HIV infection).

Gastrointestinal diseases: gastric and 12 duodenal ulcer, esophagitis, gastritis, acute or latent peptic ulcer, newly created intestinal anastomosis, nonspecific ulcerative colitis with the threat of perforation or absceration, diverticulitis.

Diseases of CCC, including recently suffered myocardial infarction (in patients with acute and subacute myocardial infarction may spread the focus of necrosis, slowing down the formation of scar tissue and as a result – rupture of heart muscle), decompensated CNS, arterial hypertension, hyperlipidemia.

Endocrine diseases: diabetes mellitus (including violation of tolerance for carbohydrates), thyrotoxicosis, hypothyroidism, Itsenko-Kushinga disease.

Severe chronic renal and/or liver failure, nephurourolithiasis.

Hypoalbuminemia and conditions predisposing to its occurrence.

Prolix Dosage Systemic osteoporosis, myasthenia gravis, acute psychosis, obesity (III-IV centuries), polio (except for the form of bulbar encephalitis), open- and closed-angle glaucoma, pregnancy, lactation period.

For intraarticular administration: patient’s general severe condition, ineffectiveness (or short duration) of the 2 previous administration (taking into account individual properties of the administered GCS).