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An equianalgesic chart is a conversion chart that lists equivalent doses of analgesics (drugs used to relieve pain). Equianalgesic charts are used for calculation of an equivalent dose (a dose which would offer an equal amount of analgesia) between different analgesics. [1]
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Free base conversion ratio Morphine (base) II: 9300 1 Morphine citrate II: 9300 0.81 Morphine bitartrate II: 9300 0.66 Morphine stearate II: 9300 0.51 Morphine phthalate II: 9300 0.89 Morphine hydrobromide II: 9300 0.78 Morphine hydrobromide (2 H 2 O) II: 9300 0.71 Morphine hydrochloride II: 9300 0.89 Morphine hydrochloride (3 H 2 O) II: 9300 0 ...
A chart outlining the structural features that define opiates and opioids, including distinctions between semi-synthetic and fully synthetic opioid structures An opiate is an alkaloid substance derived from opium (or poppy straw ). [ 1 ]
Morphine is effective and relatively safe, and is often used with moderate to severe pain. [19] Codeine and tramadol should be avoided especially in children younger than 12 years old since metabolism varies due to genetic differences between individuals, [20] and, in the case of tramadol, this medication has not been well studied in children. [21]
The BNF for Children developed from the British National Formulary (BNF), which prior to 2005 had provided information on the treatment of children, with the doses largely determined by calculations based on the body weight of the child. The guidance was provided by pharmacists and doctors whose expertise was in the care of adults.
Carbonate derivatives of 14β-hydroxycodeine "viz., 14β-hydroxy-6-O-(methoxycarbonyl)codeine, 6-O-methoxycarbonyl-14β-(methoxycarbonyloxy)codeine, and 14β-acetoxy-6-O-methoxy-carbonylcodeine, potential substrates for ring C modification in morphinane (sic) alkaloids, were synthesized for the first time."
Oxymorphone (sold under the brand names Numorphan and Opana among others) is a highly potent opioid analgesic indicated for treatment of severe pain. Pain relief after injection begins after about 5–10 minutes, after oral administration it begins after about 30 minutes, and lasts about 3–4 hours for immediate-release tablets and 12 hours for extended-release tablets. [6]