দেশ: যুক্তরাজ্য
ভাষা: ইংরেজি
সূত্র: MHRA (Medicines & Healthcare Products Regulatory Agency)
Nefopam hydrochloride
Rivopharm (UK) Ltd
N02BG06
Nefopam hydrochloride
30mg
Oral tablet
Oral
No Controlled Drug Status
Valid as a prescribable product
BNF: 04070100; GTIN: 5060388650483
Lineagrafica sa 6596 Gordola Bozza no.: 17 / Recto Data: 06.06.17 Formato: mm 190 x 240 Nefopam Hydrochloride 30 mg RIVO UK Colore: Nero In this leaflet: 1. What Nefopam tablets are and what they are used for 2. Before you take Nefopam tablets 3. How to take Nefopam tablets 4. Possible side effects 5. How to store Nefopam tablets 6. Contents of the pack and other information 1. WHAT NEFOPAM TABLETS ARE AND WHAT THEY ARE USED FOR The full name of your medicine is Nefopam Hydrochloride 30 mg Film-coated tablets. In this leaflet the shorter name Nefopam tablets is used. Nefopam tablets belong to a group of medicines called analgesics, commonly known as pain killers or pain relievers. The active substance, nefopam hydrochloride, interrupts the pain messages being sent to your brain, and it also acts in your brain to stop pain messages being felt. This means that Nefopam tablets do not stop the pain from happening, but you will not be able to feel the pain as much. Nefopam tablets are used to relieve of acute and chronic pain (for example pain after an operation, dental pain, joint or muscle pain, after an injury, or pain caused by cancer). Nefopam tablets should not be used to treat the pain from a heart attack. 2. WHAT YOU NEED TO KNOW BEFORE YOU TAKE NEFOPAM TABLETS Do not take Nefopam tablets s )FYOUAREACHILDUNDERYEARSOLD s 9OUHAVEEVERHADANALLERGICREACTIONTONEFOPAM hydrochloride or any of the ingredients resulting in a skin rash, swelling of the face of difficulty in breathing (see section 6. Contents of the pack and other information). s 9OUARETAKINGMONOAMINEOXIDASEINHIBITORS-!/)S TO treat your depression. s 9OUHAVEORHAVEEVERHADEPILEPSYlTS Warnings and precautions If the answer to any of the following is ‘yes’, you must tell your doctor – your doctor may decide to alter your treatment. s !REYOUPREGNANTORBREASTFEEDING s $OYOUHAVESEVEREPROBLEMSWITHYOURLIVERORKIDNEYS s $OYOUHAVEORHAVEYOUHADINTHEPASTDIFlCULTYPASSING URINE s !REYOUTAKINGOTHERMEDICINES Other medicines and Nefopam tablets Please tell সম্পূর্ণ নথি পড়ুন
OBJECT 1 NEFOPAM HYDROCHLORIDE 30 MG FILM-COATED TABLETS Summary of Product Characteristics Updated 15-Feb-2018 | Rivopharm UK Ltd 1. Name of the medicinal product Nefopam Hydrochloride 30 mg film-coated tablets 2. Qualitative and quantitative composition Each tablet contains 30 mg of nefopam hydrochloride. For the full list of excipients, see section 6.1. 3. Pharmaceutical form Film-coated tablets White, round, biconvex, 7.1 mm diameter tablets 4. Clinical particulars 4.1 Therapeutic indications Nefopam 30 mg tablets are indicated for the relief of acute and chronic pain, including post-operative pain, dental pain, musculo-skeletal pain, acute traumatic pain and cancer pain. 4.2 Posology and method of administration Oral use. _ADULTS_ Dosage may range from 1 to 3 tablets three times daily depending on the pain severity and the patient's response. The recommended starting dosage is 1 or 2 tablets three times daily. _SPECIAL POPULATIONS_ Children: Since the safety and efficacy of nefopam in children under 12 years has not yet been established, the administration of Nefopam 30 mg tablets is not recommended in the pediatric population. Elderly: Dosage adjustment may be required due to slower metabolism. It is strongly recommended that the starting dose does not exceed one tablet three times daily as older people appear more susceptible to, in particular, the CNS side effects of Nefopam 30 mg tablets and some cases of hallucinations and confusion have been reported in this age group. Patients with end stage renal disease: Since these patients might experience increased serum peak concentrations during treatment with nefopam, the daily dose is recommended be reduced. 4.3 Contraindications Nefopam 30 mg tablets are contraindicated in patients with hypersensitivity to the active substance or to any of the excipients listed in section 6.1. It is also contraindicated in patients with a history of convulsive disorders and should not be given to patients taking mono-amine-oxidase (MAO) inhibitors. 4.4 Special warnings and p সম্পূর্ণ নথি পড়ুন