Beechams Cold Relief Orange Flavour Effervescent Tablets
Beechams Cold Relief Orange Flavour Effervescent Tablets
Each tablet contains paracetamol 500 mg and caffeine 65 mg
Round, flat off-white, speckled tablets with a breakline mark on one side.
A mild analgesic and antipyretic formulated to give extra pain relief. The soluble tablets are recommended for the relief of common symptoms of colds and influenza, for example headache, fever, sore throat and muscular aches and pains.
4.2. Posology and method of administration
The product should be dissolved in at least half a tumbler of water.
Two tablets up to 4 times daily as required.
Do not exceed 8 tablets in 24 hours.
As for adults.
Not recommended for children under 12 years.
Method of administration
Paracetamol and caffeine 500 mg/65 mg Soluble Tablets are for oral administration only.
Hypersensitivity to paracetamol, caffeine or any of the other constituents. Patients with rare hereditary problems of fructose intolerance should not take this medicine.
Care is advised in the administration of paracetamol to patients with renal or hepatic impairment. The hazard of overdose is greater in those with non-cirrhotic alcoholic liver disease.
Excessive intake of caffeine (e.g. coffee, tea and some canned drinks) should be avoided while taking this product.
Do not exceed the stated dose.
Patients should be advised not to take other paracetamol-containing products concurrently.
Each 2 tablet dose contains 854 mg of sodium and should not be taken by patients on a low sodium diet.
If symptoms persist, consult your doctor.
Keep out of the reach and sight of children.
Immediate medical advice should be sought in the event of an overdose, even if you feel well.
Do not take with other paracetamol-containing products.
Patient. Information Leaflet:
Immediate medical advice should be sought in the event of overdose even if you feel well, because of the risk of delayed, serious liver damage.
The speed of absorption of paracetamol may be increased by metaclopramide or domperidone and absorption reduced by colestyramine. The anticoagulant effect of warfarin and other coumarins may be enhanced by prolonged regular daily use of paracetamol with increased risk of bleeding; occasional doses have no significant effect.
Paracetamol-caffeine is not recommended for use during pregnancy due to the possible increased risk of lower birth weight and spontaneous abortion associated with caffeine consumption.
Caffeine in breast milk may potentially have a stimulating effect on breast fed infants.
Due to the caffeine content of this product it should not be used if you are pregnant or breast feeding.
Adverse events from historical clinical trial data are both infrequent and from small patient exposure. Accordingly, events reported from extensive postmarketing experience at therapeutic/labelled dose and considered attributable are tabulated below by system 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.
Blood and lymphatic system disorders
Immune system disorders
Cutaneous hypersensitivity reactions including skin rashes, angiodema and Stevens Johnson syndrome/toxic epidermal necrolysis
Respiratory, thoracic and mediastinal disorders
* There have been cases of bronchospasm with paracetamol, but these are more likely in asthmatics sensitive to aspirin or other NSAIDs.
Central Nervous system
When the recommended paracetamol-caffeine dosing regimen is combined with dietary caffeine intake, the resulting higher dose of caffeine may increase the potential for caffeine-related adverse effects such as insomnia, restlessness, anxiety, irritability, headaches, gastrointestinal disturbances and palpitations.
Liver damage is possible in adults who have taken 10 g 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 the patient
a) Is on long term treatment with carbamazepine, phenobarbitone, phenytoin, primidone, rifampicin, St John’s Wort or other drugs that induce liver enzymes.
b) Regularly consumes ethanol in excess of recommended amounts. or
c) Is likely to be glutathione deplete e.g. eating disorders, cystic fibrosis, HIV infection, starvation, cachexia.
Symptoms of paracetamol overdose 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 arrythmias and pancreatitis have been reported.
Immediate treatment is essential in the management of paracetamol overdose. Despite a lack of significant early symptoms, patients should be referred to hospital urgently for immediate medical attention. Symptoms may be limited to nausea or vomiting and may not reflect the severity of the overdose or the risk of organ damage. Management should be in accordance with established treatment guidelines, see BNF overdose section.
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). 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. If required the patient should be given intravenous N-acetylcysteine, in line with the established dosage schedule. If vomiting is not a problem, oral methionine may be a suitable alternative for remote areas outside hospital. Management of patients who present with serious hepatic dysfunction beyond 24 h from ingestion should be discussed with the NPIS or a liver unit.
Overdose of caffeine may result in epigastric pain, vomitting, diuresis, tachycardia or cardia arrhythmia, CNS stimulation (insomnia, restlessness, excitement, agitation, jitteriness, tremors and convulsions).
It must be noted that for clinically significant symptoms of caffeine overdose to occur with this product, the amount ingested would be associated with serious paracetamol-related toxicity.
Patients should receive general supportive care (e.g. hydration and maintenance of vital signs). The administration of activated charcoal may be beneficial when performed within one hour of the overdose, but can be considered for up to four hours after the overdose. The CNS effects of overdose may be treated with intravenous sedatives.
High doses of sodium bicarbonate may be expected to induce gastrointestinal symptoms including belching and nausea. In addition, high doses of sodium bicarbonate may cause hypernatraemia; electrolytes should be monitored and patients managed accordingly.
The combination of paracetamol and caffeine is a well established analgesic combination.
Paracetamol is rapidly and almost completely absorbed from the gastrointestinal tract. It is relatively uniformly distributed throughout most body fluids and exhibits variable protein binding. Excretion is almost exclusively renal in the form of conjugated metabolites.
Caffeine is absorbed readily after oral administration, maximal plasma concentrations are achieved within one hour and the plasma half-life is about
3.5 hours. 65 --80% of administered caffeine is excreted in the urine as 1-methyluric acid and 1-methylxanine.
There are no preclinical data of relevance to the prescriber which are additional to that already included in other sections of the SPC.
Sodium hydrogen carbonate Sorbitol Ascorbic acid Sodium lauril sulfate Citric acid (anhydrous)
Sodium carbonate (anhydrous)
Acesulfame Potassium (E 950)
N & A Orange Flavour Aspartame (E 951)
Riboflavin sodium phosphate (E101a)
Tube: 12 months after opening
The product should be stored below 25°C.
Moisture sensitive: store the tablets in the tube, and keep the tube tightly closed. Sachet:
The product should be stored below 30°C.
Laminate sachets in cardboard cartons containing 4, 6, 12, 16, 18, 24 or 30 tablets. or
Polypropylene tubes with polyethylene stoppers containing desiccant. The container/closure system is child resistant. Each tube contains 16 effervescent tablets.
*Not all pack sizes may be marketed.
SmithKline Beecham (SWG) Limited
980 Great West Road
Trading as GlaxoSmithKline Consumer Healthcare, Brentford TW8 9GS, UK