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Beechams Cold & Flu Liquid, Cough & Congestion Relief Medicine with Paracetamol, All in One Liquid, 160 ml

£9.9£99Clearance
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Concomitant use of phenylephrine with other sympathomimetic amines can increase the risk of cardiovascular side effects. Beechams Max Strength Capsules, our STRONGEST * relief for colds, flu and chesty cough. It contains three ingredients – paracetamol, phenylephrine and guaifenesin – to provide powerful and effective relief from cold and cough symptoms. Do not take more than the recommended dose. Do not take this medicine with any other products that contain paracetamol, as this can easily result in exceeding the maximum dose of paracetamol. This medicinal product contains 19% v/v ethanol (alcohol) i.e. 3.8 ml per 20 ml dose, equivalent to 76 ml beer or 31.6 ml wine.

Hypertensive interactions occur between sympathomimetic amines such as phenylephrine and monoamine oxidase inhibitors (see contraindications).. Dosage: Adults (including elderly) and children aged 16 years and over: Cold & Flu: One sachet to be taken every four hours, if necessary, up to a maximum of six sachets in any 24 hours. Flu Plus: One sachet to be taken every four-six hours, as necessary, up to a maximum of four sachets in any 24 hours. Do not take continuously for more than 7 days without medical advice. Applies to acetaminophen / guaifenesin / phenylephrine: oral liquid. Serious side effects of Beechams All-in-One Talk to a doctor at once if you take too much of this medicine, even if you feel well. This is because too much paracetamol can cause delayed, serious liver damage.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 the ingredients of Beechams all in one. Just because a side effect is stated here doesn't mean that all people using Beechams all in one will experience that or any side effect. Patients with rare hereditary problems of galactose intolerance, the Lapp lactose deficiency or glucose-galactose malabsoption should not take this medicine. Beechams Max Strength All in One Capsules, hard (paracetamol, guaifenesin, phenylephrine hydrochloride). Adverse events from historical clinical trial data are both infrequent and from small patient exposure.

Expectorants such as guaifenesin are used to treat a productive, chesty or mucus cough, where you cough up phlegm. Guaifenesin helps to thin and loosen the mucus in the airways, making it easier to cough up. Phenylephrine overdosage is likely to result in effects similar to those listed under adverse reactions. Additional symptoms may include hypertension and possibly reflux bradycardia. In severe cases confusion, hallucinations, seizures and arrhythmias may occur. However the amount required to produce serious phenylephrine toxicity would be greater than required to cause paracetamolrelated toxicity. ParacetamolLiver damage is possible in adults who have taken 10g or more of paracetamol. Ingestion of 5g or more of paracetamol may lead to liver damage if the patient has risk factors (see below). If you're taking medicines for high blood pressure you shouldn't take Beechams all in one, because the decongestant may make your blood pressure medicine less effective.The following adverse events have been observed in clinical trials with phenylephrine and may therefore represent the most commonly occurring adverse events. The antidiabetic medicines exenatide, lixisenatide and liraglutide may slow down the absorption of paracetamol into the bloodstream, so it might take longer to work if you're using one of these medicines to treat your diabetes. Ask your pharmacist for more advice. Don't take Beechams max strength all in one if you have taken a type of medicine called a monoamine oxidase inhibitor (MAOI) in the last 14 days. MAOIs include the antidepressants phenelzine, tranylcypromine, isocarboxazid and moclobemide, and the anti-Parkinson's medicines selegiline, safinamide and rasagiline. This is because the combination of phenylephrine with these medicines could cause a dangerous increase in blood pressure (hypertensive crisis). Each 20ml liquid contains 500mg paracetamol, 200mg guaifenesin and 10mg phenylephrine. Adults and adolescents aged 12 years and over should take one 20ml measured dose (or four 5ml spoonfuls) every four hours as necessary. Do not take more than four doses in 24 hours. There are no preclinical data of relevance to the prescriber additional to that already covered in other sections of the SPC.

Drugs.com provides accurate and independent information on more than 24,000 prescription drugs, over-the-counter medicines and natural products. This material is provided for educational purposes only and is not intended for medical advice, diagnosis or treatment. Data sources include IBM Watson Micromedex (updated 1 Oct 2023), Cerner Multum™ (updated 24 Oct 2023), ASHP (updated 11 Oct 2023) and others.A minor hydroxylated metabolite which is usually produced in very small amounts by mixed-function oxidases in the liver and which is usually detoxified by conjugation with liver glutathione may accumulate following paracetamol overdose and cause liver damage. doctor or get medical help right away if you have any of the following signs or symptoms that may be related to a very bad side effect: Warnings and Precautions: Patients should be advised not to take other paracetamol-containing products concurrently, especially those with non-cirrhotic alcoholic liver disease. Do not take with other sympathomimetics, decongestants or cold and flu medicines should be avoided. Medical advice should be sought before using this product in patients with an enlargement of the prostate gland, glutathione depletion due to metabolic deficiencies, occlusive vascular disease, and cardiovascular disease. Excessive intake of caffeine should be avoided. Patients who are taking warfarin should seek medical advice before taking this product. Contains sunset yellow/ amaranth (E110) which may cause an allergic reaction. Immediate medical advice should be sought in the event of an overdose.

Events reported from extensive post-marketing experience at therapeutic/labelled dose and considered attributable are tabulated below by MedDRA System Organ Class. Events reported from extensive post-marketing experience at therapeutic/labelled dose and considered attributable are tabulated below by MedDRA System Organ Class. Due to limited clinical trial data, the frequency of these adverse events is not known (cannot be estimated from available data), but post-marketing experience indicates that adverse reactions to paracetamol are rare and serious reactions are very rare. tightness in the chest or throat; trouble breathing, swallowing, or talking; unusual hoarseness; or swelling of the mouth, face, lips, tongue, Dosage: Liquid: Adults and children 16 years and over: One 20 ml measured dose. Repeat every four hours as necessary. Do not exceed four doses per 24 hours. Do not take continuously for more than 5 days without medical advice. Not to be given to children under 16 years except on medical advice. Tablets: Adults and children 12 years and over: Two tablets. Repeat every four hours as necessary. Do not take more than 8 tablets in 24 hours. Not to be given to children under 12 years except on medical advice. If urine is collected within 24 hours of a dose of this product, a metabolite may cause a colour interference with laboratory determinations of 5 hydroxyindoleacetic acid (5- HIAA) and vanillymandelic acid (VMA). Symptoms of paracetamol overdosage in the first 24 hours are pallor, nausea, vomiting, anorexia and abdominal pain. Liver damage may become apparent 12 to 48 hours after ingestion. Abnormalities of glucose metabolism and metabolic acidosis may occur. In severe poisoning, hepatic failure may progress to encephalopathy, haemorrhage, hypoglycaemia, cerebral oedema, and death. Acute renal failure with acute tubular necrosis, strongly suggested by loin pain, haematuria and proteinuria, may develop even in the absence of severe liver damage. Cardiac arrhythmias and pancreatitis have been reported.The anticoagulant effect of warfarin and other coumarins may be enhanced by prolonged regular use of paracetamol with increased risk of bleeding; occasional doses have no significant effect. The hepato-toxicity of paracetamol may be potentiated by excessive intake of alcohol. The speed of absorption of paracetamol may be increased by metoclopramide or domperidone and absorption reduced by colestyramine.

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