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This document outlines the assessment and marketing authorisation for Paracetamol 500mg Tablets, including their uses, safety, and efficacy data as reviewed by the Medicines and Healthcare products
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How to fill out ukpar paracetamol 500mg tablets

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How to fill out UKPAR Paracetamol 500mg Tablets

01
Start by gathering all necessary materials: UKPAR Paracetamol 500mg Tablets, a prescription (if required), and a notepad for notes.
02
Read the packaging and accompanying leaflet for important safety information and dosage instructions.
03
Confirm the recommended dosage for your specific age and weight as per guidelines.
04
If you are using a prescription, ensure it is current and matches the dosage you intend to take.
05
Take the Paracetamol tablet with a full glass of water.
06
Do not exceed the maximum recommended dosage in a 24-hour period.
07
Keep a record of your dosages to avoid accidental overdose.
08
Store the tablets in a cool, dry place away from children.

Who needs UKPAR Paracetamol 500mg Tablets?

01
Individuals experiencing mild to moderate pain such as headaches, muscle aches, or toothaches.
02
People with fever conditions needing temperature reduction.
03
Patients recovering from surgery who require pain management.
04
Those advised by a healthcare professional to use paracetamol for pain relief.
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Paracetamol is a mild analgesic and antipyretic, and is recommended for the treatment of most painful and febrile conditions, for example, headache including migraine, toothache, neuralgia, colds and influenza, sore throat, backache, rheumatic pain and dysmenorrhoea.
Adults can take 2 , 500mg tablets, 4 times in 24 hours. You must wait at least 4 hours between doses. Do not take more than 8 tablets in 24 hours.
Paracetamol can take up to an hour to work. The usual dose of paracetamol is one or two 500mg tablets at a time, up to 4 times in 24 hours. The maximum dose is eight 500mg tablets in 24 hours. Do not take paracetamol with other medicines containing paracetamol because there is a risk of overdose.
Paracetamol can be given every 4 to 6 hours as required, with no more than 4 doses in 24 hours. The label on your liquid paracetamol product will have clear dosing instructions. Learn more about giving paracetamol to babies and children.
Adults can usually take 1 or 2 tablets (500mg) every 4 to 6 hours. They shouldn't take more than 4g (8x 500mg tablets) in the space of 24 hours. Always read the instructions that come with your medicine because dosage and strength of the tablet can vary. Paracetamol should start to work within an hour.
The name of your medicine is Paracetamol 500mg Tablets (called paracetamol throughout this leaflet). This medicine contains paracetamol. It belongs to a group of medicines called analgesics (painkillers) and is used to treat pain (including headache, toothache, back and period pain) and cold or flu symptoms.
Panadol 500 mg Film Coated Tablets provide temporary, effective relief from headaches, toothache, aches and pains of cold and flu, muscle aches and period pain. They also help to reduce fever. Panadol Tablets provide faster paracetamol absorption compared to standard paracetamol tablets.

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UKPAR Paracetamol 500mg Tablets are a type of medication used for the relief of pain and fever. They contain 500mg of paracetamol as the active ingredient and are commonly used to treat mild to moderate pain, such as headaches, muscle aches, and other conditions.
Manufacturers or distributors of UKPAR Paracetamol 500mg Tablets are required to file for UKPAR. This typically includes pharmaceutical companies seeking to market the product in the UK.
Filling out UKPAR involves providing detailed information about the product, including its formulation, manufacturing process, quality control measures, and clinical data demonstrating safety and efficacy. It is important to follow regulatory guidelines set by the relevant health authorities.
The purpose of UKPAR Paracetamol 500mg Tablets is to provide safe and effective pain relief and reduction of fever to patients. It acts as an analgesic and antipyretic medication.
Information that must be reported includes the product's active ingredients, dosage form, strength, indications, contraindications, potential side effects, and any relevant toxicological data, as well as details of clinical trials conducted.
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