Drugs Affecting the nervous system (CNS) Flashcards
Drugs fall into two basic categories
- stimulants(analeptics) which stimulate the nervous system
- depressants, which depress activity within the nervous system
Central nervous system drug
1) Analgesic(Narcotics)
2) Sedative/Hypnotic
3) Anesthetic
4) Anticonvulsant
Analgesics are classified as
1) agonist
2) Agonist-Antagonist
3) Antagonist
4) Anticonvulsant
Opioid Agonist
Drugs that will bind well to the receptor
ex:
Opioid Agonist-Antagonist
Drugs that have properties of both the agonist and antagonist. These drugs have some agonist and antagonist activity at the receptor sites
Opioid Antagonist
Drugs that bind to the receptor site and cause no response, agonist can reverse effects
Opioid Agonist (Action)
- do not effect nerve ending
- increase pain threshold: opioid narcotic
- causes euphoria
- changes patients perception about the pain
- alters emotional response patient has about the pain
- attitude changes pain remains the same
Opioid Agonist (Indication)
- treat mod-severe pain and manage opiate dependency
- control pain during abort(obstetric analgesia)
- mod-severe visceral pain
- can be given post op/during surgery to manage pain
- relieve anxiety
- induce mild-mod sedation
- cough suppressant
- slows respiration(side effect): used in pt who have tachypnea to slow respirations
- decrease g.i motility(anti-diarrheal)
- control anxiety on patient with mi/pe because they cause euphoria, decrease fear and anxiety about death
- decrease cardiac workload
- support anesthesia
- relieve anxiety in patients with dyspnea associated with pulmonary edema
- relieve pain associated with a myocardial infarction(morphine sulfate is agent of choice)
- induce conscious sedation before diagnostic/therapeutic procedure in the hospital setting
Opioid Agonist (origin)
obtained from opium plant. obtained from the unripe seed of the opium poppy
Codeine
- Agonist
- Opoid Analgesic
- treat mod-severe pain,ANTIUSSIVE, considered a weak analgesic
- 30-60mg
- can be added with acetaminophen(non salicylate) or ASA(Salicylate)
Equianalgesic
- term used to equivalate pain receiving properties to another drug
- all narcotics are compared to morphine
Codeine + Acetaminophen
Tylenol 1= 325mg Acetaminophen + 7.5 codeine
Tylenol 2= 325mg Acetaminophen + 15 codeine
Tylenol 3= 325mg Acetaminophen + 30 codeine
Tylenol 4= 325mg Acetaminophen + 60 codeine
Empirin
Aspirin + Codeine
Hydromorphone(Dilaudid)
- strongest opoid compound to morphine
- given 1mg can be given orally/parentally
Fentanyl
- has oral/buccal route
- Duragesic Fentanyl Transdermal
- topical drug application to skin
- systemic action
- takes time to work, change q3days
Propoxyphene(Darvon,Darvon-N)
-Propoxyphene + Acetaminophen = Darvocet N
Meperidine(Demerol)
- Agonist
- Opoid Analgesic
- treat mod-severe pain, prep sedation, anesthetic adjunct
- last about 2-3hours
- limited because causes greatest amount of hypotension
- elderly can cause paradoxical reaction: effects you dont expect(causes excitement)
- dosage 50-500mg
- synthetic developed to treat opioid withdrawal
Methadone(Dolophine)
- -Agonist
- Opoid Analgesic
- treat mod-severe pain, treat of opioid dependency
- used frequently for heroine addicts/drug abuse, treats pain,
- 10-20mg
- given by mouth usually
- used to withdraw from opioid dependency
Oxycodone(Roxicodone & Oxycontin)
- weak analgesic compared to morphine
- oxycodone + Ibprofen(Combunox)
- oxycodone + acetaminophen(Percocet)
- oxycodone + aspirin(Percodan)
-the sustained release version oxycotin, frequency q12h, effective for chronic pain=last more than 6 months, most abused opioit.
Oxycodone + aspirin(Percodan)
- opioid/non-opiod combination oral analgesic
- Oxycodone 5mg/aspirin 325mg
- narcotic medicine used to relieve moderate to severe pain.
- Percodan contains a combination of aspirin and oxycodone. Aspirin is in a group of drugs called salicylates (sa-LIS-il-ates). It works by reducing substances in the body that cause pain, fever, and inflammation. Oxycodone is an opioid pain medication. An opioid is sometimes called a narcotic.
- Percodan is used to relieve moderate to severe pain.
- Aspirin should not be given to a child or teenager who has a fever, especially if the child also has flu symptoms or chicken pox. -Aspirin can cause a serious and sometimes fatal condition called Reye’s syndrome in children.
Hydrocodone
- can be antitussive
- weak analgesic compared to morphine
Hydrocodone+Acetaminophen=vicodin
Hydrocodone+Ibuprofen=vicoprofen
Alfentanil(Alfenta)
- -Agonist
- Opoid Analgesic
- balance analgesia used to help induce analgesia
Sufentanil Citrate(Sufenta)
- -Agonist
- Opoid Analgesic
- induce and maintain analgesia
Morphine Sulfate
- -Agonist
- Opoid Analgesic
- attaches to mu receptor cite
- drug of choice for severe pain
- duration 4-5 hrs
- developed from plant prooduct white poppy plant
- opium called morphine
- all pain relieving drugs are compared to morphine
Long Acting morphine
- for mod to sever pain
- for acute pain that last several days
- also for chronic pain
ex:
-Ronal SR- last 8hrs-frequency 6A,2P,10P
dose=30mg
-MS Contin= last 12hrs last long 10A,10P
-Avina=24hrs daily dosing
Morphine Sulfate
PO: 10mg(DOSE): 10-20mins(ONSET): 60mins(PEAK): 4-5hrs(DURATION
SubQ: 4-10mg(DOSE): 10-20mins(ONSET): 30-60min(PEAK): 4-5(DURATION)
IM: 4-10mg(DOSE): 1-3mins(ONSET): 20mins(PEAK): Duration(varies)
Morphine Sulfate is drug of choice for?
mi(heart attack), pe(pulmonary edema)
Opiate Receptors
cells in the nevous system that have receptor sites
-mu and kappa receptors produce the analgesic,sedative, and euphoric effects associated with analgesic drugs
- mu,kappa, delta=located in the brain
- kapppa and delta=located in spinal coloum
- mu is important for analgesics and resp. depression and physical dependence(euphoria), morphine attaches to this receptor site and has a theraputic response
- kappa=has analgesics/resp depression(dysphoria)
mu and kappa receptors
produce the analgesic,sedative, and euphoric effects associated with analgesic drugs
mu,kappa,delta receptors
located in the brain
kapppa and delta receptors
located in spinal coloum
mu receptors
important for analgesics and resp. depression and physical dependence(euphoria), morphine attaches to this receptor site and has a theraputic response
kappa receptors
Has analgesics/resp depression(dysphoria=unwell unhappy feeling)
Side effects of Opioid Agonist:
CNS:
- Drowsiness: pronounced inthe first three days
- light headed,dizziness,euphora,
pupils:
- myosis-constriction of pupils,
- pinpoint pupil=toxcity
Resp:
-decresed respiration: treats tachypnea
Cardio:
- tachycardia
- hypotention: demerol drug
GU:
-urine retention or hesitancy
Gastrointestinal:
- N,V=more pronounced in first 3 days
- antiemtics given if needed
- decreases g.i. motility causing constipation, asses bowel sounds, develop bowel management plan
Integumentary:
- puritis,rash,utiacria
- always report rash=hypersensitivity
Contradiction of Opioid Agonist:
COPD=because causes resp depression
Head Injury:because effects cns
Pregnant females: crosses placenta barrier
Tolerance
decrease response after repeated doses
Dependency
physiological/psychological need for medication
Addiction
change in behavioral patterns
Withdrawal
cessation(abprut stopping), results in diarrhea,stomach cramps, sneezing,runny nose, yawning,irritablility,nervousness, and large pupils
- methadone(treats withdrawal, manage pain)
- levomethodyl given for withdrawal when methadone is not effective anymore than put back on methadone in 2 day period
Opoid Agonist-Antagonist(Action)
- effect kappa and delta receptor sites
- for patient who cant tolerate agonist
- less respiratory depression and less dependency
Opoid Agonist-Antagonist(side effects)
- sedation,N&V,headache,dizzinesss(vertigo),euphoria,hallucination
- withdrawal can occur in patients addicted to opiates
Opoid Agonist-Antagonist(Drugs)
1-Pentazocine Lactate
- Pentazocine and ASA (Talwin)
- Pentazocine and Tylenol (Talacen)
2-Butorphanol (Stadol)
3-Nalbuphine(HCL)-pain manangement in pregnancy
- Burenorphine(Buprenex,Subutex, Butrans)
- Buprenorphine & Naloxone(Suboxone)-C3, used to treat opoid dependency
Butorphanol(stadol)
- Opoid Agonist-Antagonist(Drugs)
- Butorphanol tartrate is a synthetically derived opioid agonist-antagonist analgesic of the phenanthrene series.
- Stadol (butorphanol tartrate) Injection and Stadol NS (butorphanol tartrate) Nasal Spray are indicated for the management of pain when the use of an opioid analgesic is appropriate.
-Stadol Injection is also indicated as a preoperative or preanesthetic medication, as a supplement to balanced anesthesia, and for the relief of pain during labor.
Opoid Antagonist
action:
- prevents or revereses opiate effects
- may restore resp function in 1-2min
- adverse effect-increase cns activity reversal of analgesic
- indication: pain relieving ability will be reversed
Drugs:
- Naltexone HCL(Revia,Vivitrol)
- Revia: used to decrease cravings for alcohol
- Naloxone HCL(Narcan)
Naloxone HCL(narcan)
- Naloxone is an special narcotic drug that reverses the effects of other narcotic medicines.
- Naloxone is used to reverse the effects of narcotic drugs used during surgery or to treat pain.
- 0.4 to 2 mg/dose IV/IM/subcutaneously.
Non-Narcotic Analgesic
NSAID=Toradol=im/iv Acetaminophen(Tylenol)=hepatotocity, activated charcol Acetylsalicylic acid(Asprin)
Migraine Headaches
vascular headaches caused when blood vessels dialte in head
3 groups of drugs used for migraine headaches
1-analgesics: non narcotic analgesic,saliclates(ASA),NSAIDS(Ibprofen),Acetaminophen(tylenol)
2-ergot derivatives
3-triptans