Nuromol Pain Relief Tablets, Paracetamol and Ibuprofen, Pack Of 16, From The Makers Of Nurofen

Product Information

The elderly are at increased risk of the serious consequences of adverse reactions. If an NSAID is considered necessary, the lowest effective dose should be used for the shortest possible duration. The patient should be monitored regularly for gastrointestinal bleeding during NSAID therapy. People with an active peptic ulcer or bleeding in the gut; those who've had two or more episodes of this in the past; and people who have ever experienced bleeding or perforation in the gut as a result of taking an NSAID. Take 1 tablet to be taken with water and food , up to three times a day. Leave at least 6 hours between doses.

Nurofen Plus vs Nuromol: What is the difference? - Versus Nurofen Plus vs Nuromol: What is the difference? - Versus

Paracetamol is excreted in breast milk but not in a clinically significant amount. Available published data do not contraindicate breastfeeding. In patients with a history of, or an existing gastrointestinal ulceration/perforation or bleeding, including that associated with NSAIDs (see section 4.4). Appropriate monitoring and medical advice are required for patients with a history of hypertension and/or mild to moderate congestive heart failure as fluid retention, hypertension and oedema have been reported in association with NSAID therapy. Nuromol is not recommended for women who are trying to get pregnant because NSAIDs like ibuprofen can temporarily reduce female fertility. Treatment with N-acetylcysteine may be used up to 24 hours after ingestion of paracetamol, however; the maximum protective effect is obtained up to 8 hours post ingestion. The effectiveness of the antidote declines sharply after this time.

Patient leaflet - NUROMOL DUAL ACTION 200 MG 500 MG FILM-COATED TABLETS

Experimental data suggest that ibuprofen may competitively inhibit the effect of low dose acetylsalicylic acid on platelet aggregation when they are dosed concomitantly. Some pharmacodynamic studies show that when single doses of ibuprofen 400 mg was taken within 8 h before or within 30 min after immediate release acetylsalicylic acid dosing (81 mg), a decreased effect of acetylsalicylic acid on the formation of thromboxane or platelet aggregation occurred. Although there are uncertainties regarding extrapolation of these data to the clinical situation, the possibility that regular, long-term use of ibuprofen may reduce the cardioprotective effect of low-dose acetylsalicylic acid cannot be excluded. No clinically relevant effect is considered to be likely for occasional ibuprofen use (see section 4.5). include agranulocytosis, anaemia, aplastic anaemia, haemolytic anaemia leucopenia, neutropenia, pancytopenia and thrombocytopenia. Treatment with activated charcoal should be considered if the overdose has been taken within 1 hour. Plasma paracetamol concentration should be measured at 4 hours or later after ingestion (earlier concentrations are unreliable). If the pain has not been relieved by ibuprofen or paracetamol during the first day of treatment, then the next day Nuromol Dual Action can be taken. Paracetamol IV is used for the management of mild to moderate pain, the management of moderate to severe pain with adjunctive opioid analgesics, the reduction of fever.

Nuromol : Uses, Dosage, Side Effects, FAQ - MedicinesFAQ Nuromol : Uses, Dosage, Side Effects, FAQ - MedicinesFAQ

Patients with a history of GI toxicity, particularly the elderly, should report any unusual abdominal symptoms (especially GI bleeding) particularly in the initial stages of treatment. By combining the two active ingredients, Paracetamol and Ibuprofen, Nuromol Tablet can be considered an alternative to codeine-based analgesics for short-term management of moderate pain in patients unable to take non-steroidal anti-inflammatory drugs. liver problems (causing yellowing of the skin and white of eyes) • kidney problems (causing increased or decreased urination, swelling of the legs) • heart failure (causing breathlessness, swelling) Caution is advised if paracetamol is administered concomitantly with flucloxacillin due to increased risk of high anion gap metabolic acidosis (HAGMA), particularly in patients with severe renal impairment, sepsis, malnutrition and other sources of glutathione deficiency (e.g. chronic alcoholism), as well as those using maximum daily doses of paracetamol. Close monitoring, including measurement of urinary 5-oxoproline, is recommended. Antiplatelet agents and selective serotonin reuptake inhibitors (SSRIs): Increased risk of gastrointestinal bleeding (see section 4.4).if you experience: • heartburn, indigestion • signs of intestinal bleeding (severe stomach pain, vomiting blood or liquid with what looks like coffee