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ANALGESICS
ANALGESIC

A drug that selectively relieves pain by acting
 on CNS or on peripheral pain mechanisms
 without significantly altering consciousness
ALGESIA or PAIN
It is an illdefined, unpleasent sensation,
 usually evoked by an external or internal
 noxious stimulus
PAIN RECEPTOR
 Pain receptor in our bodies are nerves that transmit pain.
  These are free nerve endings located in various body
  tissues that respond to thermal, mechanical, & chemical
  stimuli.

 When tissue becomes injured, they release chemicals
  called prostaglandins and leukotrienes that make the
  pain receptor more sensitive and these causing pain.
Types of Pain
                        Visceral
        According to
           source       Somatic
                       Neuropathic
PAIN
                          Acute
       According to
        chronicity       Chronic
Therapeutic management of pain
Classification:
  Peripheral (miscellaneous):
          -Causal
          -Non causal
  Central:
          -Narcotic
          -Non narcotic
Peripheral Analgesic
Causal:               Non-causal:
    -Treat the cause        -Not treat the cause
    eg:- atropine      Examples:
                       1- Local anesthetics (for
                          superficial tumor)
                       2- Counter-irritant (apply
                          pain that counteract or
                          mask the original one e.g.
                          acupuncture)
Central Analgesic
Opioids:              NSAIDs:
    Morphine &             1- Aspirin
 morphine like drugs       2- Paracetamol
                           3- Diclofenac
                           4- Piroxicam
                           5- Ibuprofin
                           6- Ketoprofin
OPIOID ANALGESIC
“Opium” is a Greek word meaning “juice,” or
 the exudates from the poppy.
Opium is extracted from poppy seeds (Paper
 somniforum)
“Opioid” is a natural or synthetic drug that
 binds to opioid receptors producing agonist
 effects.
Fresh capsule of opium poppy   Cut capsule showing latex
                                    exuding from cut
Classification
                    Based on
                                     According to
Chemically          receptor
                                       source
                   occupation

  Phenanthrene        Agonists         Natural opium
     group                               alkaloids
  Eg: Morphine      Eg: Morphine       Eg: Morphine

 Benzolisoquino     Antagonists        Semisynthetic
   line group                           derivatives
  Eg: Papaverine    Eg: Naloxone        Eg: Heroine

                    Mixed agonist-       Synthetic
                     antagonist           opioids
                    Eg: Nalorphine     Eg: Pethidine
MORPHINE
• Morphine is the most important alkalloid of
  opium.

• Many new opioids have been synthesized but
  none of them are superior to morphine as an
  analgesic.

• It is the protype of this group.
Mechanism of Action
   Opioids exert their major effects by interacting with opioid receptors in the CNS
   Opioids activate 7- transmembrane GPCRs located pre-symaptically and post-symaptically along pain
    transmission pathways.
   High densities of opioid receptors known as mu, delta and kappa are found in the dorsal horn of the
    spinal cord and higher CNS centers.
   Most currently used opioid analgesics act mainly at mu- opioid receptors
   Morphine acts at kappa receptors in lamina 1 and 11 of the substantia Granulose of the spinal cord
    and decreases the release of substance p, which is modulates pain perception in the spinal cord.
   Opioids have an onset of action that depends on the route of administration .
   Opioids causes hyper polarization of nerve cells , inhibition of nerve firing and presynaptic inhibition
    of transmitter relea
   Cellular effects of these drugs involve enhancement of neuronal potassium efflux ( hyperpolarizes
    neurons and makes them less likely to respond to a pain stimulus ) and inhibition of calcium influx (
    decreases neuro- transmitter release from neurons located along the pain transmission pathway )
   Opioids relieve pain both by raising the pain threshold at the spinal cord level and more importantly by altering the brains
    perception of pain
Pharmacological actions
   Analgesia
   Respiratory depression
   Cough suppression
   Vagal stimulation (bradycardia)
   Sedation & hypnosis
   Hypothermia
   Itching
   Physical & pshycological dependence
   Euphoria
   Histamine release , hypotension….etc
Adverse effects
•   Morphine can produce a wide range of adverse effects like nausea, vomiting, dizziness,
    mental clouding, respiratory depression, constipation, dysphoria, urinary retention, &
    hypotension, allergic reactions.
•   Tolerance- Repeated administration of morphine results in the development of tolerance to
    some of its effects including respiratory depression, analgesia, sedation, etc .
•   Dependence- Opium has been a drug of addiction for many centuries. Its ability to produce
    euphoria makes it a drug of addiction. Opioids produce both physiological & pshycological
    dependence. Manifestations are lacrimination, sweating, yawning, anxiety, restlessness..etc.
NSAIDs
Non steroidal anti-inflamatory drugs
 are aspirine-type or non-opioid
 analgesics.
In addition they have anti-
 inflamatory, anti pyretic &
 uricosuric properties without
 addiction liability.
Classification
       Non selective COX
         inhibitor
    • Salicylic acid derivatives. Eg:
                   aspirine
                                        Selective
  • Para aminophenol derivatives.
               Eg: paracetamol          COX-2
      • Pyrazolone derivatives. Eg:
              Sphenylbutazone
• Indole acetic acid derivatives. Eg:
                                        inhibitors
                   sulindac
   • Arylacetic acid derivatives. Eg:
                  diclofenac
   • Propionic acid derivatives. Eg:
                                        • Nimesulidde,
                  ibuprofen
  • Anthralinic acid derivatives. Eg;
                                          celecoxib,
               flufenamic acid
         • Oxicams. Eg: piroxicam         rofecoxib…etc
      • Alkanones. Eg: nabumetone
Mechanism of action
                                         Arachidonic acid




                    COX-1                                        COX-2

                                                                                         COX-2
                                             NSAIDs                                    inhibitors


              LeukotrienesPr
                                                            Prostaglandins
                ostaglandins

Primarily support    Primarily protect
                                                               Primarily mediate
platelet function    GI-tract mucosa                        inflamation, fever, pain
Pharmacological actions
•   Analgesia
•   Antipyretic actions
•   Anti-inflamatory actions
•   Respiration stimulation
•   Metabolic effects
•   Immunological effects
•   Uric acid excretion
•   Blood- delayed clotting time
Adverse effects
  Analgesics doses are usually well tolerated but anti-inflamatory doses are
      usually associated with adverse effects whed used for a long period.
A. G.I tract:- Epigastric distress, nausea, vomiting, erosive gastritis, peptic
   ulcer, increase occult blood loss in stools are common
B. Allergic reactions are not common and may be manifested as rashes,
   photo sensitivity..etc
C. Haemolysis
D. Nephrotoxicity
E. Reye’s syndrome
F. Salicylism
G. Acute salicylate intoxication
Analgesics used in deintistry
• Non opiod analgesics are mostly used for mild to
  moderate pain.
• NSAIDs
     COX1 & COX2:
          Ibuprofen, aspirin, ketrolac, diclofenac
     COX-2:
          celecoxib, rofecoxib, nimesulide.
Acetaminophen
• Dose:
     -Adult: 0.5 – 1g every 4-6 hrs.
     -6-12 years: 250-500mg every 4-6hrs.
     -1-5 years: 150-250mg every 4-6hrs.

• Contraindication:
     Renal failure, asthma, liver failure.
Nimesulide
• Indication:- Acute pain

• Dose:- 100mg twice a day

• Contraindication:- Renal failure, asthma,
  liver                  failure
OPIOIDS
Although opiod as a class are
effective analgesics, some
commonly formulation shows poor
analgesic efficacy for dental pain,
and is not used for their adverse
effects.
Tramadol
• Tramadol is a synthetic centraly acting
  analgesic indicated to moderate to
  moderately severe pain.
• Dose:- 50-100mg every 4-6 hours.
          (400mg/day- maximum)
Combination!!
• Analgesic monotherapy has shown
  equivocal success in treating
  dental pain.
• The goal of combining analgesics
  with different mechanisms of
  action is to use lower doses of the
  component drugs.
Acetaminophen combination
• Acetaminophen is an effective analgesic for mild pain, but to
  manage more severe pain it typically is combined with
  codeine or one of its derivatives.
• Acetaminophen 1000mg combined with codeine 60mg.
• Acetaminophen 1000mg combined with oxycodone 10mg.
• Acetaminophen 650mg combined with tramadol 75mg.
• Acetaminophen 500mg combined with hydrocodone 7.5mg.
NSAIDs Combination
• Ibuprofen 400mg combined with
  codeine 60mg.
• Ibuprofen 400mg combined with
  oxycodone 10mg.
• Ibuprofen 400mg combined with
  hydrocodone 15mg.
THANK YOU

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Analgesics kp

  • 2. ANALGESIC A drug that selectively relieves pain by acting on CNS or on peripheral pain mechanisms without significantly altering consciousness
  • 3. ALGESIA or PAIN It is an illdefined, unpleasent sensation, usually evoked by an external or internal noxious stimulus
  • 4. PAIN RECEPTOR  Pain receptor in our bodies are nerves that transmit pain. These are free nerve endings located in various body tissues that respond to thermal, mechanical, & chemical stimuli.  When tissue becomes injured, they release chemicals called prostaglandins and leukotrienes that make the pain receptor more sensitive and these causing pain.
  • 5. Types of Pain Visceral According to source Somatic Neuropathic PAIN Acute According to chronicity Chronic
  • 6. Therapeutic management of pain Classification: Peripheral (miscellaneous): -Causal -Non causal Central: -Narcotic -Non narcotic
  • 7. Peripheral Analgesic Causal: Non-causal: -Treat the cause -Not treat the cause eg:- atropine Examples: 1- Local anesthetics (for superficial tumor) 2- Counter-irritant (apply pain that counteract or mask the original one e.g. acupuncture)
  • 8. Central Analgesic Opioids: NSAIDs: Morphine & 1- Aspirin morphine like drugs 2- Paracetamol 3- Diclofenac 4- Piroxicam 5- Ibuprofin 6- Ketoprofin
  • 9. OPIOID ANALGESIC “Opium” is a Greek word meaning “juice,” or the exudates from the poppy. Opium is extracted from poppy seeds (Paper somniforum) “Opioid” is a natural or synthetic drug that binds to opioid receptors producing agonist effects.
  • 10. Fresh capsule of opium poppy Cut capsule showing latex exuding from cut
  • 11. Classification Based on According to Chemically receptor source occupation Phenanthrene Agonists Natural opium group alkaloids Eg: Morphine Eg: Morphine Eg: Morphine Benzolisoquino Antagonists Semisynthetic line group derivatives Eg: Papaverine Eg: Naloxone Eg: Heroine Mixed agonist- Synthetic antagonist opioids Eg: Nalorphine Eg: Pethidine
  • 12. MORPHINE • Morphine is the most important alkalloid of opium. • Many new opioids have been synthesized but none of them are superior to morphine as an analgesic. • It is the protype of this group.
  • 13. Mechanism of Action  Opioids exert their major effects by interacting with opioid receptors in the CNS  Opioids activate 7- transmembrane GPCRs located pre-symaptically and post-symaptically along pain transmission pathways.  High densities of opioid receptors known as mu, delta and kappa are found in the dorsal horn of the spinal cord and higher CNS centers.  Most currently used opioid analgesics act mainly at mu- opioid receptors  Morphine acts at kappa receptors in lamina 1 and 11 of the substantia Granulose of the spinal cord and decreases the release of substance p, which is modulates pain perception in the spinal cord.  Opioids have an onset of action that depends on the route of administration .  Opioids causes hyper polarization of nerve cells , inhibition of nerve firing and presynaptic inhibition of transmitter relea  Cellular effects of these drugs involve enhancement of neuronal potassium efflux ( hyperpolarizes neurons and makes them less likely to respond to a pain stimulus ) and inhibition of calcium influx ( decreases neuro- transmitter release from neurons located along the pain transmission pathway )  Opioids relieve pain both by raising the pain threshold at the spinal cord level and more importantly by altering the brains perception of pain
  • 14.
  • 15. Pharmacological actions  Analgesia  Respiratory depression  Cough suppression  Vagal stimulation (bradycardia)  Sedation & hypnosis  Hypothermia  Itching  Physical & pshycological dependence  Euphoria  Histamine release , hypotension….etc
  • 16. Adverse effects • Morphine can produce a wide range of adverse effects like nausea, vomiting, dizziness, mental clouding, respiratory depression, constipation, dysphoria, urinary retention, & hypotension, allergic reactions. • Tolerance- Repeated administration of morphine results in the development of tolerance to some of its effects including respiratory depression, analgesia, sedation, etc . • Dependence- Opium has been a drug of addiction for many centuries. Its ability to produce euphoria makes it a drug of addiction. Opioids produce both physiological & pshycological dependence. Manifestations are lacrimination, sweating, yawning, anxiety, restlessness..etc.
  • 17. NSAIDs Non steroidal anti-inflamatory drugs are aspirine-type or non-opioid analgesics. In addition they have anti- inflamatory, anti pyretic & uricosuric properties without addiction liability.
  • 18. Classification Non selective COX inhibitor • Salicylic acid derivatives. Eg: aspirine Selective • Para aminophenol derivatives. Eg: paracetamol COX-2 • Pyrazolone derivatives. Eg: Sphenylbutazone • Indole acetic acid derivatives. Eg: inhibitors sulindac • Arylacetic acid derivatives. Eg: diclofenac • Propionic acid derivatives. Eg: • Nimesulidde, ibuprofen • Anthralinic acid derivatives. Eg; celecoxib, flufenamic acid • Oxicams. Eg: piroxicam rofecoxib…etc • Alkanones. Eg: nabumetone
  • 19. Mechanism of action Arachidonic acid COX-1 COX-2 COX-2 NSAIDs inhibitors LeukotrienesPr Prostaglandins ostaglandins Primarily support Primarily protect Primarily mediate platelet function GI-tract mucosa inflamation, fever, pain
  • 20. Pharmacological actions • Analgesia • Antipyretic actions • Anti-inflamatory actions • Respiration stimulation • Metabolic effects • Immunological effects • Uric acid excretion • Blood- delayed clotting time
  • 21. Adverse effects Analgesics doses are usually well tolerated but anti-inflamatory doses are usually associated with adverse effects whed used for a long period. A. G.I tract:- Epigastric distress, nausea, vomiting, erosive gastritis, peptic ulcer, increase occult blood loss in stools are common B. Allergic reactions are not common and may be manifested as rashes, photo sensitivity..etc C. Haemolysis D. Nephrotoxicity E. Reye’s syndrome F. Salicylism G. Acute salicylate intoxication
  • 22. Analgesics used in deintistry • Non opiod analgesics are mostly used for mild to moderate pain. • NSAIDs COX1 & COX2: Ibuprofen, aspirin, ketrolac, diclofenac COX-2: celecoxib, rofecoxib, nimesulide.
  • 23. Acetaminophen • Dose: -Adult: 0.5 – 1g every 4-6 hrs. -6-12 years: 250-500mg every 4-6hrs. -1-5 years: 150-250mg every 4-6hrs. • Contraindication: Renal failure, asthma, liver failure.
  • 24. Nimesulide • Indication:- Acute pain • Dose:- 100mg twice a day • Contraindication:- Renal failure, asthma, liver failure
  • 25. OPIOIDS Although opiod as a class are effective analgesics, some commonly formulation shows poor analgesic efficacy for dental pain, and is not used for their adverse effects.
  • 26. Tramadol • Tramadol is a synthetic centraly acting analgesic indicated to moderate to moderately severe pain. • Dose:- 50-100mg every 4-6 hours. (400mg/day- maximum)
  • 27. Combination!! • Analgesic monotherapy has shown equivocal success in treating dental pain. • The goal of combining analgesics with different mechanisms of action is to use lower doses of the component drugs.
  • 28. Acetaminophen combination • Acetaminophen is an effective analgesic for mild pain, but to manage more severe pain it typically is combined with codeine or one of its derivatives. • Acetaminophen 1000mg combined with codeine 60mg. • Acetaminophen 1000mg combined with oxycodone 10mg. • Acetaminophen 650mg combined with tramadol 75mg. • Acetaminophen 500mg combined with hydrocodone 7.5mg.
  • 29. NSAIDs Combination • Ibuprofen 400mg combined with codeine 60mg. • Ibuprofen 400mg combined with oxycodone 10mg. • Ibuprofen 400mg combined with hydrocodone 15mg.