Summary of Product Characteristics (SmPC) - Paracetamol 500 mg effervescent tablets
1 NAME OF THE MEDICINAL PRODUCT
Paracetamol 500 mg Effervescent Tablets
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
Each effervescent tablet contains:
Paracetamol 500 mg
Excipients with known effect:
Each tablet contains approximately 102mg of lactose
Each tablet contains approximately 315 mg of sodium
For the full list of excipients, see section 6.1
3 PHARMACEUTICAL FORM
Effervescent Tablets
Round, biplane, white or off-white tablets with facets on both sides.
4 CLINICAL PARTICULARS
4.1 Therapeutic indications
For the relief of mild to moderate pain including headache, migraine, neuralgia, toothache, period pain and pain caused by rheumatism.
It is also used to relieve the symptoms of colds, flu and sore throats.
4.2 Posology and method of administration
Adults and children over 15 years:
One or two tablets to be taken every four to six hours if necessary. Do not exceed 8 tablets in 24 hours.
Children 12 to 15 years:
| Age | Recommended Dose | 500mg tablet dose | How often |
| 12-15 years | 480-750mg | One – One and a half | Every 4-6 hours when necessary to a maximum of 4 doses in 24 hours |
Children under 12 years.
Not to be given to children under 12 years.
Elderly patients:
Normal adult dose unless there is impaired kidney or liver function.
Directions:
The tablets must be dissolved in a glass of water. The tablets dissolve more quickly in warm water if stirred.
4.3 Contraindications
Hypersensitivity to the active substance or to any of the excipients listed in section 6.1.
4.4 Special warnings and precautions for use
Care is advised in the administration of paracetamol to patients with severe renal or severe hepatic impairment and in those with non-cirrhotic alcoholic liver disease. The hazards of overdose are greater in those with alcohol liver disease.
Do not take more medicine than the label tells you to. If you do not get better, talk to your doctor.
Contains Paracetamol.
Do not take anything else containing paracetamol while taking this medicine.
Talk to your 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.
Patients should be advised that paracetamol may cause severe skin reactions. If a skin reaction such as skin reddening, blisters, or rash occurs, they should stop use and seek medical assistance right away.
Each tablet contains approximately 315 mg of sodium. This sodium should be taken into account when prescribing for patients on a sodium restricted diet. Each tablet contains approximately 102mg of lactose. Patients with rare hereditary problems of galactose intolerance, the Lapp lactase deficiency or glucose-galactose malabsorption should not take this medicine.
Cases of high anion gap metabolic acidosis (HAGMA) due to pyroglutamic acidosis have been reported in patients with severe illness such as severe renal impairment and sepsis, or in patients with malnutrition or other sources of glutathione deficiency (e.g. chronic alcoholism) who were treated with paracetamol at therapeutic dose for a prolonged period or a combination of paracetamol and flucloxacillin. If HAGMA due to pyroglutamic acidosis is suspected, prompt discontinuation of paracetamol and close monitoring, is recommended. The measurement of urinary 5-oxoproline may be useful to identify pyroglutamic acidosis as underlying cause of HAGMA in patients with multiple risk factors.
4.5 Interaction with other medicinal products and other forms of interaction
Cholestyramine: The speed of absorption of paracetamol is reduced by cholestyramine. Therefore, the cholestyramine should not be taken within one hour if maximal analgesia is required.
Metoclopramide and Domperidone: The absorption of paracetamol is increased by metoclopramide and domperidone. However, concurrent use need not be avoided.
Warfarin: 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.
Chloramphenicol: Increased plasma concentration of chloramphenicol.
Caution should be taken when paracetamol is used concomitantly with flucloxacillin as concurrent intake has been associated with high anion gap metabolic acidosis due to pyroglutamic acidosis, especially in patients with risks factors (see section 4.4)
4.6 Fertility, pregnancy and lactation
Pregnancy
A large amount of data on pregnant women indicate neither malformative, nor feto/neonatal toxicity. Epidemiological studies on neurodevelopment in children exposed to paracetamol in utero show inconclusive results. If clinically needed, paracetamol can be used during pregnancy however it should be used at the lowest effective dose for the shortest possible time and at the lowest possible frequency.
Breast-feeding
Paracetamol is excreted in breast milk but not in a clinically significant amount.
Available published data do not contraindicate breast-feeding.
4.7 Effects on ability to drive and use machines
None known
4.8 Undesirable effects
Adverse effects of Paracetamol are rare. Very rare cases of serious skin reactions have been reported. There have been reports of blood dyscrasias including thrombocytopenia purpura, methaemoglobenaemia and agranulocytosis, but these were not necessarily causally related to Paracetamol.
| System organ class | Frequency | Undesirable effects |
| Metabolism and nutrition disorders | ‘’Not known’’ (cannot be estimated from the available data) | High anion gap metabolic acidosis Cases of high anion gap metabolic acidosis due to pyroglutamic acidosis have been observed in patients with risk factors using paracetamol (see section 4.4). Pyroglutamic acidosis may occur as a consequence of low glutathione levels in these patients. |
Reporting of suspected adverse reactions
Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via the Yellow Card Scheme website www.mhra.gov.uk/yellowcard.
4.9 Overdose
Liver 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).
Risk Factors 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.
Or
- 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
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.
Management
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 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.
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 hours from ingestion should be discussed with the NPIS or a liver unit.
5 PHARMACOLOGICAL PROPERTIES
5.1 Pharmacodynamic properties
Pharmacotherapeutic group: Analides, Other Analgesics and Antipyretics.
ATC Code: N02B E01
Mechanism of action
Analgesic – the mechanism of analgesic action has not been fully determined. Paracetamol may act predominantly by inhibiting prostaglandin synthesis in the central nervous system (CNS) and to a lesser extent, through a peripheral action by blocking pain-impulse generation.
The peripheral action may also be due to inhibition of prostaglandin synthesis or to inhibition of the synthesis or actions of other substances that sensitise pain receptors to mechanical or chemical stimulation.
Antipyretic – paracetamol probably produces antipyresis by acting centrally on the hypothalamic heat-regulation centre to produce peripheral vasodilation resulting in increased blood flow through the skin, sweating and heat loss. The central action probably involves inhibition of prostaglandin synthesis in the hypothalamus
5.2 Pharmacokinetic properties
Absorption and Fate
Paracetamol is readily absorbed from the gastrointestinal tract with peak plasma concentrations occurring 30 minutes to 2 hours after ingestion. It is metabolised in the liver and excreted in the urine mainly as the glucuronide and sulfate conjugates. Less than 5% is excreted as unchanged paracetamol. The elimination half-life varies from about 1 to 4 hours. Plasma-protein binding is negligible at usual therapeutic concentrations but increases with increasing concentrations.
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 overdosage and cause liver damage.
5.3 Preclinical safety data
Conventional studies using the currently accepted standards for the evaluation of toxicity to reproduction and development are not available.
6 PHARMACEUTICAL PARTICULARS
6.1 List of excipients
Citric acid
Lactose monohydrate
Sodium hydrogen carbonate
Povidone
Simethicone emulsion
Saccharin sodium
Lemon flavour, containing citral, citric acid, ethyl alcohol, lemon oil, lime oil, alphatocopherol, triacetine, maltodextrin, gum arabic and sucrose Sodium content approximately 315 mg per tablet
6.2 Incompatibilities
Not applicable.
6.3 Shelf life
3 years.
6.4 Special precautions for storage
Polypropylene tube:
Do not store above 25°C. Keep the container tightly closed.
Strip Pack:
Store in the original package in order to protect from moisture.
6.5 Nature and contents of container
Polypropylene tube:
Polypropylene tube with polyethylene stopper containing silica gel as desiccant. The tubes are packed into an outer carton.
Pack sizes: 16 / 32 / 60 / 100.
Strip Pack:
4 ply Laminate of Paper / PE Extrusion I Aluminium Foil/I PE Extrusion on both sides of strip.
or
Plain unprinted 4-layer Laminate of Paper/PE/Aluminium Foil/ Surlyn and Aluminium foil, soft dull side laminated to paper and bright side Surlyn Coated
Pack sizes: 32, 60, 100 tablets.
Not all pack sizes may be marketed
6.6 Special precautions for disposal
None.
7 MARKETING AUTHORISATION HOLDER
Steranco Healthcare UK Limited
Unit 2A, Olympic Way,
Sefton Business Park,
Bootle, Merseyside
L30 1RD, United Kingdom
8 MARKETING AUTHORISATION NUMBER(S)
PL 60260/0026
9 DATE OF FIRST AUTHORISATION/RENEWAL OF THE
AUTHORISATION
11/11/2025
10 DATE OF REVISION OF THE TEXT
11/11/2025