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  • ParacetamolNimesulide

  • Humanity has but three great enemies; Fever, Famine and War. Of these by far the most terrible , is fever.

    ( Sir William Osler )

  • Pathogenesis of feverInfectious agents or toxin ( Endo/Exo)Mediators of inflammationMonocyte/MacrophagesEndothelial cells and other cell typeCorticosteroidPyogenic cytokinesIL 1 alpha and betaTNF,IL_6, IFNSEnhanced immunity

    Archidonic Acid

    PGF2COX2AntipyreticAnterior hypothalamusElevation ofThermoregulatorySet pointIncreased heat productionIncreased heat conservationFever

  • MODE OF ACTIONTissue damage, release of pyrogens and phospholipids from cell membraneArchidonic acidNSAID blockCOX 1*and COX 2in periphery and CNSParacetamol blocks COX 2 and COX 3 ?in CNSPG3

    PG3

    PG3

    Fever and PainCOX 1* is critical to maintain the integrity of platelets,renal function and gastric mucosa.

  • Choice of antipyretic is highly debatable

    Which should the choice

    Safety. Wide therapeutic window. Short duration of action. Side effect: Over dosing either intentional or accidental.

  • Choice of antipyretic

    According to WHO paracetamol is the drug of first choice* .

    Ibuprofen is a useful 2nd line drug.

    No other NSAID including Nimesulide should be prescribed for children with high grade fever and used with caution has been cleared by US FDA for using as antipyretic.* WHO 1990

  • PCM was first used clinically by Von Mering in 1893.Marketed in US - 1950. in UK- 1956Well tolerated . Rarely produce side effects of any kind when administered in recommended doses.

  • Paracetamol approved FDA (USA)

    OTC status since 1955.

    Consider safer in asthmatic patients.

  • Pharmacokinetics:

    PCM bio availability above 80% .

    Peak plasma concentration occur between 15 mins and 2 hours after ingestion.

    It has few Pharmacokinetics drug interaction.

  • Adverse effects.

    Excellent safety records at therapeutic doses.

    Excellent safety in patient of all age.

    PCM no associated risk of major upper GI bleed or mucosal damage.

  • Side Effect

    Haemostasis Meth- haemoglobinaemia. Thrombocytopenia. Anaemia. Agranulocytosis. Hepatotoxicity. Nephrotoxicity

  • Contraindication and precaution

    Apart from hypersensitivity, No absolute contraindication. Suitable in all areas with a wide range of medical conditions Children Elderly Patients with mild to moderate liver disease , renal disease,GI problems. Asthmatics

  • PCM overdose

    Excellent safety and tolerability. Effective antidote for PCM available. Therapeutic overdose is rare. Acute toxic dose 150 mg/kg or 10 times the recommended dose. Over dose is usually suicidal and appropriate over a period of time.

  • Nimesulide :-

    Long duration of action.

    Small therapeutic window.

    Easy Overdosing negligence or ignorance.

    Serious infection may be missed.

    May cause hypotension occasionally.

    Many countries have withdrawn

  • Nimesulide

    NSAID with selective COX2 inhibitory action. Peak 1 4hrs after intake. Marginal better than paracetamol. Patient in long term use must be monitored for side effect.

  • Side effects of Antipyretic

    Adverse effectPCMNSAID GI side effectRare + + Skin RashRare + + RO bleedingNil + +Bronchial hyper-reactivityNil + Hepato-toxicity+ + + + ( overdose) ( Overdose) Nephrotoxicity + + +National Kidney foundation USA, PCM Safe. SeizureNil + HypothermiaNil + PregnancySafeunsafe < 6 month RecommendedNot recommended