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Codeine/paracetamol, also called codeine/acetaminophen and co-codamol, is a compound analgesic, comprising codeine phosphate and paracetamol (acetaminophen). Codeine/paracetamol is used for the relief of mild to moderate pain when paracetamol or non-steroidal anti-inflammatory drugs (NSAIDs; such as ibuprofen, aspirin, and naproxen) alone do not sufficiently relieve symptoms.
Co-dydramol is a non-proprietary name used to denote a particular compound analgesic, a combination of dihydrocodeine tartrate and paracetamol. Co-dydramol tablets are used for the relief of moderate pain. Co-dydramol is part of a series of combination drugs available in the UK and other countries including co-codaprin (aspirin and codeine).
Codeine is used to treat mild to moderate pain. [4] It is commonly used to treat post-surgical dental pain. [13]Weak evidence indicates that it is useful in cancer pain, but it may have increased adverse effects, especially constipation, compared to other opioids. [14]
So when I go to the page for Tylenol, it states that Tylenol 1 contains 8 mg codeine, 2 contains 15 mg, 3 contains 30 mg, 4 contains 60 mg (all of which, so far, I know first-hand to be correct) and finally, that Tylenol 5 contains 90 mg of codeine. However, this page states that they only go up to Tylenol 4 and that 60 mg is the maximum dosage ...
AC&C is available in different formulations containing varying amounts of codeine. Formulations containing 8 mg or less of codeine ("AC&C 8" or "222") are typically available from pharmacies over the counter. A prescription is not required, but the medication must be requested from the pharmacist.
[7] [8] It is not available in the United Kingdom, [9] though the combination codeine/paracetamol (co-codamol) is. [10] It is sold under the brand names Vicodin and Norco among others. [ 1 ] [ 2 ]
1998 advertisement. Solpadeine is the brand name of a range of analgesic medication containing various amounts of paracetamol, ibuprofen, caffeine and codeine, made by Omega Pharma. [1]
Paracetamol's bioavailability is dose-dependent: it increases from 63 % for 500 mg dose to 89 % for 1000 mg dose. [6] Its plasma terminal elimination half-life is 1.9–2.5 hours, [ 6 ] and volume of distribution is roughly 50 L. [ 132 ] Protein binding is negligible, except under the conditions of overdose, when it may reach 15–21 %. [ 6 ]