Mefenamic acid is used for the short-term relief of mild to moderate pain from various conditions such as headache, dental pain, menstrual cramps, and muscle aches
A black box warning alerts doctors and patients about drug effects that may ‐ The active substance is mefenamic acid
Indications and dose Acute pain including dysmenorrhoea, Menorrhagia By mouth Child 12–17 years 500 mg 3 times a day
Mefenamic acid is a nonsteroidal anti-inflammatory drug (NSAID) that is used short-term (7 days or less) to treat mild to moderate pain in adults and children who
It is most often used for treating pain of dysmenorrhoea in the short term
Some prostaglandins are produced at sites of injury or damage, and cause pain and inflammation
Mefenamic acid 500 mg film-coated tablets Active Ingredient: mefenamic acid
Unit 4, Metro Centre, Tolpits
Mefenamic acid is known as a Mefenamic Acid tablets contain mefenamic acid which is a non-steroidal anti-inflammatory drug (NSAID)
Mefenamic acid is a white to off white, crystalline powder with a melting point of about 230°C-231°C and water solubility of 0
Children younger than 14 years of age—Use and dose must be determined by your doctor
Mefenamic acid is also licensed for the treatment of dysmenorrhoea; however, it can cause seizures in overdose
It helps to relieve pain and cramps during
Local fibrinolysis: The recommended standard dosage is 15-25 mg/kg bodyweight (i
Mefenamic acid 250mg tablets Alliance Healthcare (Distribution) Ltd Show Cautionary and advisory labels
Drug tariff Part VIIIA Category C
2
It is used to relieve mild to moderate pain, including Mefenamic acid is a member of the anthranilic acid derivatives (or fenamate) class of nonsteroidal anti-inflammatory drugs (NSAIDs), and is used to treat mild to moderate pain
- Keep this leaflet
It may Mefenamic Acid suspension contains mefenamic acid which is a non-steroidal anti-inflammatory drug (NSAID)
Sau khi uống thuốc nên ngồi nghỉ ngơi khoảng 10 phút trước khi đi nằm
Child: As oral susp: >6 months to <2 years 25 mg/kg Mefenamic acid was less potent than flufenamic acid in this model