Pharmacopeia

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Field NSAIDS – IBUPROFEN
Neurology & Sedation · Neurology & Sedation · Level 3
PARACETAMOL
Neurology & Sedation · Neurology & Sedation · Level 1
Mechanism of action

Reversibly inhibits COX 1 and 2 enzymes
causing decreased production of prostaglandin precursors

Not entirely elucidated
1. Reduced prostaglandin synthesis in areas of inflammation ? COX 3 inhibition
a) ↓ PGE2 in Hypothalamus → Anti-pyretic effect
2. Analgesic Effect
a) ↓’d central serotonergic reuptake → ↑ descending
b) 5HT agonist → enhanced descending inhibitory pain pathways.
c) Central inhibition of endocannabinoid uptake
d) Peripheral afferent nociceptive chemoreceptor impulse blockade via bradykinin inhibition
synergistic with opioid medications,
reducing the overall opioid requirement by 20-30%

Physiological effects

As an anti-inflammatory, anti-pyretic and mild analgesic

Functional class: Antipyretic, Analgesic
Indications: Mild-moderate pain, Opioid sparing, Antipyretic

Absorption

Rapidly absorbed
85% bioavailability

PO bioavailability 60-90% (Small intest)

Distribution

pKa 4.5, weak acid therefore mostly unionised, abs via gut and SB

Lipid solubility intermediate
pKa 9.5

Protein binding

99% protein bound (may displace highly protein bound drugs such as warfarin altering PD properties)

Low protein binding (5%)

Volume of distribution

Very small Vd 0.1L/kg

Vd = 1L/kg

Metabolism

hepatic via oxidation

Metabolised by the liver to glucuronide, sulphate and cysteine conjugates.

Excretion

excreted as metabolites in urine 1% unchanged

Renal excretion of glucuronide, sulphide metabolites. Inactive, build up in renal failure.

Half-life

half life 2-3 hours

half life ~2 hours
- prolonged in overdosage and renal dx.

Adverse Effects Toxicity

Worsen renal function by inhibiting PGE2 and causing vasoconstriction.
 risk of thromboembolic events.
Increased risk of GI bleeding and ulceration, GORD.
Impair platelet function
May reduce the beneficial eff¬ects of aspirin

Very safe SE profile. Safe in ped,preg.
Toxicity – hepatic and renal toxicity. plasma levels should be plotted on a nomogram and consideration of NAC infusion commenced as appropriate. ALT is a marker of damage.

Class Group

Non-Opiate Analgesic

Non-Opiate Analgesic

Indications Uses

Analgesia
Antipyretic
Antiinflammatory

Analgesia
Anitpyretic

Introduction

non selective cycloxygenase inhibitor

Acetanalide derivative

Legacy Cicm Level

Level 3

Level 1

Onset Peak Duration

onset 30 mins, duration 6 hours

onset / duration PO <1 hr / 4-6 hrs, IV 10-15mins / 4-6 hrs

Presentation

200mg tablets, some formulations in combination with codiene

Tablets, IV formulation with 10mg/mL containing mannitol, Combination formulations with codeine and non-steroidals

Route And Dose

Tablets for PO/PR

Route: Tablets, IV
Dose: 15mg/kg to 1g QID