Exam 1 Pcol 2 Flashcards
Morphine
Ms
Mu Agonist
Ms Cotin, Kadian
Codeine
Mu Agonist
Meperidine
D
Mu receptor agonist
Demerol
Hydrocodone extended release
z
Mu receptor agonist
Zohydro
Hydrocodone + Acetaminophen
v
Mu receptor agonist
Vicodin
Hydrocodone + homatropine
h
Mu receptor agonist + muscarinic antagonist
Hycodan
Tramadol
u
Mu receptor agonist
Can also directly activate a2 receptors and will inhibit the reuptake of 5-HT and norepinephrine
can lead to serotonin syndrome–> tweaking
Ultram
Tapentadol
n
Mu receptor agonist
will also inhibit the reuptake of norepinephrine
Nucynta
Oxycodone ER
O
Mu receptor agonist
Oxycotin
Oxycodone + acetaminophen
P
Mu receptor agonist
Percocet
Oxycodone + aspirin
P
Mu receptor agonist
Percodan
Methadone
Mu receptor agonist
Dolophine
Hydromorphone
D
Mu receptor agonist
Dilaudid
Oxymorphone
Mu receptor agonist
Levorphanol
Levo-d
Mu receptor agonist
levo-dromoran
Fentanyl
Mu receptor agonist
Duragesic, actiq
Alfentanil
Mu receptor agonist
Remifentanil
Mu receptor agonist
Sufentanil
Ds
Mu receptor agonist
Dsuvia
Oliceridine
oli
Mu receptor agonist
Biased ligand
Olinvyk
Diphenoxylate + atropine
lom-
periphery Mu receptor agonist
lomotil
Loperamide
im-
periphery Mu receptor agonist
imodium
DTO
Periphery Mu agonist
Deoderize tincture of opium
Naloxone
Mu antagonist
Narcan
Nalmefene
rev
Mu antagonist
Revex
Naltrexone
Viv-
Mu antagonist
vivitrol
Methylnaltrexone
re
Periphery Mu antagonist
relistor
Naloxegol
Mova
think movan (muevan)
periphery Mu antagonist
movantik
Naldemedine
symp
Periphery Mu antagonist
Symproic
Alvimopan
ent
Periphery Mu antagonist
Entereg
Nalbuphine
Nub-
Kappa agonist/Mu antagonist
Nubian
Butorphanol
Kappa agonist/Mu antagonist
Pentazocine
Kappa agonist/Mu antagonist
Buprenorphine
sub
Mu partial agonist / Kappa antagonist
has hugh affinity to Mu receptors but very little intrinsic activity so less withdrawal symptoms
Subutex
Buprenorphine + Naloxone
Partial mu Agonist / Mu antagonist
Suboxone
Ziconotide
pri
Conotoxin peptide drug
cause the closing of the N-type Ca2+ channels in the dorsal horn / spinal cord so no activation of the ascending neurons
Can treat chronic pain
Prialt
Sumatriptan
im-
Triptans
Activate 5-HT 1B and 5-HT 1D
Imitrex
Almotriptan
Ax-
Triptan
Activate 5-HT 1B and 5-HT 1D
Axert
Zolmitriptan
Zo-
Triptans
Activate 5-HT 1B and 5-HT 1D
Zomig
Naratriptan
Amer-
Triptan
Activate 5-HT 1B and 5-HT 1D
Amerge
Rizatriptan
Max-
Triptans
Activates 5-HT 1B and 5-HT 1D
Maxalt
Frovatriptan
Triptan
Activate 5-HT 1B and 5-HT 1D
Frova
Eletriptan
Rel-
Triptan
activate 5-HT 1B and 5-HT 1D
Relpax
Ergotamine
Ergots
Activate 5-HT 1B , 5-HT 1D, can directly activate A1 receptors that are Gq, activate 5-HT 2a receptors in the uterus
Dihydroergotamine
Ergots
Activate 5-HT 1B receptor in the blood vessles , 5-HT 1D receptor in the presynaptic, 5-HT 2a receptor in the uterus smooth muscle
And directly activates A1 receptor
Methylergonovine
Ergot
Activate 5-HT 2a receptor in the uterus and is use to stop post-partum bleeding
methergine
Lasmiditan
rey-
Ditans
Activate 5-HT 1F and reduces the release of CGRP
Reyvow
Ubrogepant
u-
Gepants
CGRP Competitive antagonist
Ubrelvy
Rimegepant
nu-
Gepans
CGRP competitive antagonist
Nurtec ODT
Atogepant
qui-
Gepans
CGRP competitive antagonist
Quilipta
Zavegepant
Zav-
Gepans
CGRP competitive antagonist
Zavzpret
Aimovig
Monoclonal antibody
CGRP antagonist
Ajovy
Monoclonal antibody
CGRP antagonist
Emgality
Monoclonal antibody
CGRP antagonist
Vyepti
Monoclonal antibody
CGRP antagonist
Treximet
Sumatriptan (imitrex) + Naproxen (naprosyn)
Fiorinal
A B C
Aspirin + Butalbital + Caffeine
Fioricet
A B C
Acetaminophen + Butalbital + Caffeine
Benzo’s -am
Midazolam
Ve-
MIDA VE REMI BY TRI HALCON
Benzodiazepine
Positive allosteric modulator enhances GABA by binding to the intercept between Y2 and A1
Short Acting
Use for:
-Anxiety provoking events
-Produces brief sedation for short procedure and calms the pt
-Use hypnotic effect–> Pt has trouble falling asleep
Versed
Remimazolam
MIDA VE REMI BY TRI HALCON
Benzo
Positive allosteric modulation –> Enhances GABA
Binds to the intercept between Y2 and A1
Use for:
-Anxiety provoking events
-Produces brief sedation for short procedure and calms the pt
-Use hypnotic effect–> Pt has trouble falling asleep
Byfavo
Triazolam
MIDA VE REMI BY TRI HALCON
Benzo = -am
Positive allosteric modulator enhances GABA by binding to the intercept between Y2 and A1
Short acting
Use for:
-Anxiety provoking events
-Produces brief sedation for short procedure and calms the pt
-Use hypnotic effect–> Pt has trouble falling asleep
Halcion
Alprazolam
X
Benzo –> Intermediate acting
Postiive allosteric modulator binds in between the Y2 and A1 intercept and enhances GABA activity
-Use for anxiety
Xanax
Estazolam
p-
Benzo –> Intermediate acting
Positive allosteric modulator
enhances GABA by binding in between the Y2 and A1 intercept
-Use for anxiety
Prosom
Lorazepam
Benzo –> Intermediate acting
Positive allosteric modulator –> bind in between the Y2 and A1 intercept and enhances GABA activity
-Use for anxiety
Ativan
Oxazepam
Se- think Sera
Benzodiazepine–> Intermediate acting
Positive allosteric modulator it binds in between the Y2 and A1 intercept and enhances GABA
-Use for anxiety
Serax
Temazepam
Re-
Benzodiazepine–> intermediate acting
Positive allosteric modulator –> Binds in between the Y2 and A1 intercept and enhances GABA
-Use for anxiety
Restoril
Flunitrazepam
Roh-
Benzodiazepine –> Intermediate acting
Positive allosteric modulator binds in between the Y2 and A1 intercept enhacing GABA
Use for anxiety
Rohypnol
Chlordiazepoxide
li-
Benzo–> Long acting
Positive allosteric modulator binds in between the Y2 and A1 intercept and will enhance GABA
Use for:
Anxiolytic
Hypnotic–> Trouble maintaining sleep
Myorelaxant
Anticonvulsant
librium
Clobazam
o-
Benzo –> Long acting
Binds inbetween the A1 and Y2 intercept and enhances GABA is a positive allosteric
Use for:
Anxiolytic
Hypnotic–> Trouble maintaining sleep
Myorelaxant
Anticonvulsant
Onfi
Clonazepam
K
Benzo–> Long acting
It binds inbetween the y2 and A1 intercept and enhances GABA activity is a positive allosteric modulation
Use for:
Anxiolytic
Hypnotic–> Trouble maintaining sleep
Myorelaxant
Anticonvulsant
Klonopin
Clorazepate
T-
Benz–> Long acting
Positive allosteric modulator binds next to the intercet of Y2 and A1 and enhances GABA activity
Use for:
Anxiolytic
Hypnotic–> Trouble maintaining sleep
Myorelaxant
Anticonvulsant
Tranxene
Diazepam
Can give by injection as organic salt for anticonvulsion
Give PO for Hypnolytic and anxiolytic
Benzo –> Long acting
Positive allosteric modulator binds in between the Y2 and A1 intercept and enhances GABA
Use for:
Anxiolytic
Hypnotic–> Trouble maintaining sleep
Myorelaxant
Anticonvulsant
Valium
Flurazepam
Dal-
Long acting benzo
Positive allosteric modulator –> Binds in between the Y2 and A1 intercept and enhances GABA activity
Use for:
Anxiolytic
Hypnotic–> Trouble maintaining sleep
Myorelaxant
Anticonvulsant
Dalmane
Quazepam
Think doral bank
Long acting Benzo
Positive allosteric modulator binds in between the Y2 and A1 intercept and enhances GABA activity
Use for:
Anxiolytic
Hypnotic–> Trouble maintaining sleep
Myorelaxant
Anticonvulsant
Doral
Flumazenil
Benzodiazepine receptor antagonist
It binds in between the Y2 and A1 intercept and prevent the benzodiazepines from binding
-Has no effect on GABA
Zolpidem
ZolA Zale Son Eszo Lunes
Z compound
Is a positive allosteric modulator it binds to the GABA A receptor the one that has the A1 receptor that is found primarly in areas of the brain that produces Sedation and hypnotic effects
Ambien
Zaleplon
ZolA Zale-Son Eszo Lunes
Z-compound
Positive Allosteric Modulator it binds to the GABA A receptor the one that has A1 receptor that is in areas of the brain that produces Sedation and Hypnotic effects
Sonata
Eszopiclone
ZolA Zale Son Eszo Lunes
Z compound
Is a positive allosteric modulator it binds to the GABA A receptor the one that has the A1 receptor so is use because of its hypnotic effects
Lunesta
Thiopental
Ultra-Short acting barbiturate
Positive allosteric modulator –> Binds to the GABA A receptor that has any A and B subunit and enhances GABA a inhibitor N.S
It can also bind to AMPA receptor and block Glutamate from binding (Glutamate is a excitatory N.S)
Use IV as pre-anesthesia
Methohexital
-th-
Ultra-short acting barbiturates
Positive allosteric modulator –> Binds to GABA A receptor the ones that contain any A and B subunit and enhances GABA activity (inhibitory n.s) Cl- enter hyperpolarize the cell
-It can also bind to AMPA receptors and block Glutamate from binding (a excitatory n.s)
-Use for anesthesia in surgery
Secobarbital
sec-
Short acting Barbiturate
-Positive allosteric modulator –> Binds to GABA A receptor the ones that have A and B subunit and enhances GABA activity (inhibitory N.S and Cl- enter hyperpolarize the cell)
-Can bind to AMPA receptors and block Glutamate from binding (excitatory n.s)
-Use for physician assistant suicide
Seconal
Pentobarbital
nem-
Short acting Barbiturate
Positive allosteric modulator–> Binds to GABA A receptor the ones that have any A and B subunit and enhances GABA activity (inhibitory n.s Cl- enters hyperpolarize the cell)
-Can also bind to AMPA receptors and block Glutamate (excitatory n.s ) from binding
-Use for pre-anesthesia
-Was used for insonmnia
Nembutal
Butalbital
Intermediate Barbiturate
-Positive allosteric modulator –> Binds to GABA A receptors the ones that have A and B subunit and enhaces GABA activity (a inhibitory n.s and Cl- enters hyperpolarize the cell)
-Can also bind to AMPA receptors and will block Glutamate from binding
-Use for sedating the pt
-Was used for insomnia
Phenobarbital
Lu-
Long acting Barbiturate
-Positive allosteric modulator –> Binds to GABA A receptors the ones that have A and B subunit and enhances GABA activity (inhibitory n.s)
-Can also bind to AMPA receptors and prevent glutamate from binding (excitatory n.s)
-Use as anticonvulsant as a Na+ salt injection
-Used to be use for insonmnia by PO
Luminal
Melatonin
MT1 and MT2 receptor agonist
MT1 –> Associated with hypnotic effects
MT2–> Associated with reset of the circadiam rhythm
-Melatonin is produce endogenous by the pineal gland in the bran and follows the circadiam rhythm
High during night
Low during day
Ramelteon
(Roz-)
-melteon =
think rozemos
MT1 and MT2 agonist
But is somewhat more selective for MT1
MT1 receptor is associated with Hypnotic effects
Use Ramelteon (Rozerem) for insomnia
Rozerem
Tasimelteon
-Melteon=
Hetl-
MT1/MT2 agonist
Tasimelteon is more selective for MT2 receptor that is associated with reset of circadiam rhythm
Is use to treat non-24 sleep wake disorder in a pt that is blind
Hetlioz
-Oxerant=
Suvorexant
(Bels-
DORA’s
Dual Orexin Receptor Antagonist
-Suvorexant (Belsomra) will block oxerin from binding to its receptor –> Therefore Oxerin won’t be able to produce its wakefulness effects
-Use for hypnotic –> Help pt fall asleep
Belsomra
-OREXANT =
Lemborexant
(Day-
DORA= Dual Orexin Receptor Antagonist
Orexin is peptide in the brain that is associated with Wakefulness
But Lemborexant (Dayvigo) will prevent orexin from binding
-Use for Hypnotic effect–> Help pt fall asleep
Dayvigo
-OREXANT =
Daridorexant
(Quvi-
DORA’s
Dual Oxerin Receptor Antagonist
Oxerin is peptide in the brain that is associated with wakefulness
But Daridoxerant (Quviviq) will block oxerin from binding and produces hypnotic effect
-Use to help pt fall asleep
Quviviq
Buspirone
Bus-
5-HT1A Partial agonist
It will activate 5-HT1A receptors that are in the pre-synaptic and will cause less release of 5-HT onto post synaptic 5-HT receptors (Serotonin causes anxiety)
-By reducing the release of 5-HT from the presynaptic it causes Anxiolytic effects but it takes time weeks to develop the anxiolytic effects
-Only use for chronic anxiety not for acute anxiety (event provoking anxiety)
-Can also be use in pt that have substance abuse behavior and want to stay away from Benzodiazepines and Z drugs (Zola Zale Son Eszo Lunes)
-Does not produce sedation and no hypnotic effects
Buspar
Baclofen
Lio-
Centrally acting muscle relaxant works in the spinal cord
-Work as a GABA B receptor agonist (GABA B is link to Gi)
-Use for chronic muscle spasm
-Can cause physical dependence so need to tapper down the dose because if the pt suddenly stop can suffer from withdrawals hallucinations
Lioresal
Tizanidine
Zana-
Is a Centrally Acting Muscle relaxant
Is a A2 agonist
Activates A2 receptors in the pre-synapse –> K+ Channels open K+ leaves and cause hyperpolarization –> Less release of glutamate
Activates A2 receptors in the post-synapse motor neuron–> K+ channels open K+ leaves causes the motor neuron to be more negative and wont be able to generate impulses to the skeletal muscle
Zanaflex
Cyclobenzaprine
Flex-
Centrally acting muscle relaxant
-Works by a indirect mechanism –> Inhibit the reuptake of Norepinephrine at the A2 receptors therefore indirectly causes increase activation of the A2 receptors in the presynaptic neuron –> So less release of glutamate
In the postsynaptic–> K+ leaves so the post-synaptic motor neuron wont be able to generate impulses down to the skeletal muscle
-Block Histamine H-1 receptors
-Block Muscarinic receptors
Flexeril
Carisoprodol
Think Soma the bras brand
Centrally acting muscle relaxant
-Carisoprodol (Soma) is converted into is active metabolite that is Meprobamate
Meprobamate will have similar effects like barbiturates –> Binds to the GABA A receptor and enhances GABA activity at the GABA A so Cl entry –> The post synaptic motor neuron is hyperpolarize and cannot generate impulses to the skeletal muscle
-Use as muscle relaxant
Soma
Orphenadrine
Nor-
Centrally acting Muscle relaxant
-It blocks the NMDA receptor (A ligand gated receptor in the post synaptic motor neuron) and prevent Glutamate from binding so no Na+ entry –> The motor neuron won’t be able to generate impulses to the skeletal muscle
-Block Histamine-H1 receptors
-Block Muscarinic receptors
Norflex
Methocarbamol
Roba-
Centrally acting muscle relaxant
It blocks NMDA receptors (Ligand gated) in the post-synaptic motor neuron so Block glutamate from binding so no Na+ entry –> No generation of impulses to the skeletal muscle
-Block Histamine H1 receptors
Block Muscarinic receptors
Robaxin
Dantrolene
D-
Direct acting muscle relaxant –> Does not work in the CNS it works directly in the Skeletal muscle
-Inhibits the release of Ca2+ from the sarcoplasmic reticulum –> So no Ca2+ to work on the skeletal muscle –> No muscle contraction
-Is also use as a antidote when someone uses succinylcholine and the pt has a genetic polymorphism and suffers from malignant hyperthermia
Dantrium