Ország: Egyesült Királyság
Nyelv: angol
Forrás: MHRA (Medicines & Healthcare Products Regulatory Agency)
Methocarbamol
Almirall Ltd
M03BA03
Methocarbamol
750mg
Oral tablet
Oral
No Controlled Drug Status
Valid as a prescribable product
BNF: 10020200; GTIN: 5022690000127
PACKAGE LEAFLET: INFORMATION FOR THE PATIENT ROBAXIN ®- 750 750 MG FILM-COATED TABLETS FOR ORAL USE Methocarbamol 100 Tablets Dosage: 2 tablets to be swallowed 4 times a day or as directed by your doctor. Please read the enclosed leaflet Each tablet contains methocarbamol 750mg. Also contains: maize starch, sodium lauryl sulphate, hypromellose and propylene glycol. Keep out of the sight and reach of children Warning: May cause drowsiness. If affected, do not drive or operate machinery. Avoid alcoholic drink. READ ALL OF THIS LEAFLET CAREFULLY BEFORE YOU START TAKING THIS MEDICINE BECAUSE IT CONTAINS IMPORTANT INFORMATION FOR YOU. - Keep this leaflet. You may need to read it again. - If you have any further questions, ask your doctor or pharmacist. - This medicine has been prescribed for you only. Do not pass it on to others. It may harm them, even if their signs of illness are the same as yours. - If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. See section 4. WHAT IS IN THIS LEAFLET 1. What Robaxin-750 is and what it is used for 2. What you need to know before you take Robaxin-750 3. How to take Robaxin-750 4. Possible side effects 5. How to store Robaxin-750 6. Contents of the pack and other information 1. WHAT ROBAXIN-750 IS AND WHAT IT IS USED FOR Robaxin-750 contains the active ingredient methocarbamol (750mg) which belongs to a group of medicines called muscle relaxants. Robaxin-750 is used for the short-term treatment of pain and muscle spasm caused by injuries such as sprains and strains. 2. WHAT YOU NEED TO KNOW BEFORE YOUR TAKE ROBAXIN-750 DO NOT TAKE ROBAXIN-750 IF YOU: • are allergic to methocarbamol, or have had any problems in the past with medicines containing methocarbamol • are allergic to any of the other ingredients of this medicine (listed in section 6) • have ever suffered any brain damage or coma • suffer from epilepsy or convulsions • suffer from muscle weakness (a disease called myasthenia gravis) Olvassa el a teljes dokumentumot
OBJECT 1 ROBAXIN-750 Summary of Product Characteristics Updated 08-Aug-2017 | Almirall Limited 1. Name of the medicinal product Robaxin-750, 750 mg film-coated tablets 2. Qualitative and quantitative composition Each white, capsule-shaped tablet contains 750 mg methocarbamol. For the full list of excipients, see section 6.1. 3. Pharmaceutical form Film-coated tablet. 4. Clinical particulars 4.1 Therapeutic indications As a short-term adjunct to the symptomatic treatment of acute musculoskeletal disorders associated with painful muscle spasms. 4.2 Posology and method of administration For oral use. Posology Adults: The usual dose is 2 tablets four times daily but therapeutic response has been achieved with doses as low as 1 tablet three times daily. Elderly: Half the maximum dose or less may be sufficient to produce a therapeutic response. _Paediatric population_ Not recommended. _Hepatically impaired_ In patients with chronic hepatic disease the elimination half-life may be prolonged. Therefore, consideration should be given to increasing the dose interval. 4.3 Contraindications Hypersensitivity to methocarbamol or to any of the excipients listed in section 6.1. Coma or pre-coma states. Known brain damage or epilepsy. Myasthenia gravis. 4.4 Special warnings and precautions for use Robaxin-750 should be used with caution in patients with renal and hepatic insufficiency. 4.5 Interaction with other medicinal products and other forms of interaction This product may potentiate the effects of other central nervous system depressants and stimulants including alcohol, barbiturates, anaesthetics and appetite suppressants. The effects of anticholinergics, e.g. atropine and some psychotropic drugs, may be potentiated by methocarbamol. Methocarbamol may inhibit the effect of pyridostigmine bromide. Therefore methocarbamol should be used with caution in patients with myasthenia gravis receiving anticholinesterase agents. Little is known about the possibility of interactions with other drugs. Methocarbamol may cause colour int Olvassa el a teljes dokumentumot