How does it work?
Methylprednisolone acetate is a type of medicine known as a corticosteroid. Corticosteroids are hormones produced naturally by the adrenal glands which have many important functions, including control of inflammatory responses.
Methylprednisolone acetate is a synthetic corticosteroid and is used to decrease inflammation. It works by acting within cells to prevent the release of certain chemicals that are important in the immune system. These chemicals are normally involved in producing immune and allergic responses, resulting in inflammation. By decreasing the release of these chemicals in a particular area, inflammation is reduced. This can help control a wide number of disease states, characterised by excessive inflammation.
Methylprednisolone acetate is given by injection directly into a joint, tendon or the tissue around a joint, to relieve inflammation and pain and increase mobility of the affected joint, in inflammatory conditions such as arthritis.
Methylprednisolone acetate is used in much higher doses than the levels of corticosteroids produced naturally by the body, and as such, the usual actions of corticosteroids become exaggerated and can be observed as side effects of this medicine.
Lidocaine (lignocaine) hydrochloride is a local anaesthetic. It works by temporarily reducing the passage of pain signals along nerve fibres. This allows pain relief in the area where the medicine has been injected.
What is it used for?
Inflammation of the envelope (bursa) found around parts of the body which are subject to friction e.g. joints, muscles and tendons (bursitis)
Joint injection in inflammatory disease of the joints (e.g. rheumatoid arthritis)
Joint injection in osteoarthritis with associated inflammation
Soft tissue injection in e.g. inflammation of a tendon (tendonitis)
Warning!
A steroid card will be supplied with this medicine. This contains details of the prescriber, type of steroid and dose taken and the duration of treatment. It should be carried at all times.
If individuals have not had chickenpox, they should avoid close personal contact with people with chickenpox or shingles (herpes zoster). If exposed, seek urgent medical attention as these diseases can be life-threatening in people whose immune system is suppressed.
This medicine should not be stopped abruptly but tapered down, especially when taken for longer than 3 weeks. The natural production of corticosteroids by the adrenal glands is suppressed by this medicine and the body therefore becomes reliant on it.
This medicine may increase susceptibility to infections and also mask the symptoms of these infections.
Although oral and injected corticosteroids are banned by the international olympic committee, injections of corticosteroids into joints are not.
Following joint injection, the occurrence of a distinct increase in pain accompanied by swelling, further restriction of joint movement, fever and malaise are suggestive of an infected arthritis. Antimicrobial treatment should be given to treat this complication.
Injections administered into joints are associated with a risk of infection. Any fluid present in the joint should be examined to exclude bacterial infection before starting treatment. These injections should only be given under sterile conditions.
Use with caution in
Abnormal muscle weakness
Abscess or other infections producing pus
Adolescents
Children
Decreased kidney function
Diabetes
Elderly people
Epilepsy
Family history of diabetes
Family history of glaucoma
Glaucoma
Heart failure
Herpes simplex virus infection of the eye
High blood pressure
History of drug allergy
History of or current mental disorder
History of steroid induced mental disturbances
Hypothyroidism
Inflammation of small sac-like structures which sometimes form in the walls of the intestine (diverticulitis)
Inflammation of the bowel and back passage
Liver cirrhosis
Liver failure
Osteoporosis
Peptic ulcer
Post-menopausal women
Premature infants
Previous muscle disease (myopathy) caused by steroids
Recent surgical procedure involving the joining together of ends of the intestine after a section has been removed (intestinal anastomosis)
Schizophrenia
Tendency for inflammation of a vein associated with blood clot formation (thrombophlebitis)
Tuberculosis
Not to be used in
Allergy to other local anaesthetics (amide type)
Infection of the joint or surrounding tissue (joint injection only)
Infection throughout the body (systemic infection) unless treated with specific anti-infectives
Injection into a vein (intravenous injection)
Injection into the achilles tendon
Injection into the spinal cord (intrathecal injection)
Injection into unstable joints
This medicine should not be used if you are allergic to one or any of its ingredients. Please inform your doctor or pharmacist if you have previously experienced such an allergy.
If you feel you have experienced an allergic reaction, stop using this medicine and inform your doctor or pharmacist immediately.
Pregnancy and Breastfeeding
Certain medicines should not be used during pregnancy or breastfeeding. However, other medicines may be safely used in pregnancy or breastfeeding providing the benefits to the mother outweigh the risks to the unborn baby. Always inform your doctor if you are pregnant or planning a pregnancy, before using any medicine.
This medicine should be used with caution during pregnancy, and only if the expected benefit to the mother is greater than the possible risk to the foetus. Seek medical advice from your doctor.
This medicine passes into breast milk. Discuss its use during breastfeeding with your doctor.
Side effects
Medicines and their possible side effects can affect individual people in different ways. The following are some of the side effects that are known to be associated with this medicine. Because a side effect is stated here, it does not mean that all people using this medicine will experience that or any side effect.
Blurred vision
Changes in mood
Increased pressure inside the eye (glaucoma)
Weight gain
Decreased functioning of the adrenal gland (adrenal suppression)
Thinning of the bones (osteoporosis)
Ulceration of the stomach or intestine
Increased susceptibility to infections
Acne
An extreme allergic reaction (anaphylaxis)
Increased risk of fractures of the bones
Lightheadedness
Slow heart rate (bradycardia)
Increased hair growth (hirsutism)
Skin thinning
Supression of growth in children and adolescents
Initial flare up of condition following joint injection
The side effects listed above may not include all of the side effects reported by the drug's manufacturer.
For more information about any other possible risks associated with this medicine, please read the information provided with the medicine or consult your doctor or pharmacist.
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