Use LEFT and RIGHT arrow keys to navigate between flashcards;
Use UP and DOWN arrow keys to flip the card;
H to show hint;
A reads text to speech;
127 Cards in this Set
- Front
- Back
strong mu agonists
|
morphine
hydromorphone oxymorphone methadone meperidine fentanyl sufentanil remifentanil levorphanol |
|
antitussives
|
dextromethorphan
codeine levopropoxyphene |
|
mild to moderate agonists
|
codeine
oxycodone hydrocodone propoxyphene diphenoxylate loperamide |
|
opioids used for diarrhea
|
diphenoxylate
loperamide |
|
mixed agonists/antagonists/and partial agonists
|
nalbuphine
buprenorphine butorphanol pentazocin |
|
opioids that cause increase in HR and BP
|
butorphanol
pentazocine |
|
tramadol
|
inhibits serotonin and NE
less resp. depression less neonatal resp. depresion |
|
opioid antagonists
|
naloxone
naltrexone nalmefene |
|
naloxone
|
opioid overdose
|
|
naltrexone
|
ETOH addiction
|
|
mechanism of opioids
|
inhibit adenylyl cyclase activity
inhibit presynaptic Ca influx and activation of postsynaptic K channels in the dorsal horn of the spinal cord reduce neurotransmitter release: NE, substance P, glutamate, serotonin |
|
highly lipophilic opioid
|
fentanyl
|
|
1000x more potent than morphine
|
sufentanil
|
|
inhibit synthesis of peptidoglycan by inhibiting transpeptidase
|
penicillin
|
|
anti-pseudomonal penicillins
|
ticarcillin
mezlocillin |
|
inhibit beta lactamases
|
clavulanate
sulbactam tazobactam |
|
augmentin
|
amoxacillin + clavulanate
|
|
unasyn
|
ampicillin + sulbactam
|
|
zocyn
|
pipercillin + tazobactam
|
|
inhibit transpeptidase blocking cross link formation of peptidoglycan
|
cephalosporins
|
|
cephalosporin to treat gonorrhea
|
3rd generation
|
|
cephalosporin to treat pseudomonas
|
cefepime
|
|
inhibits transpeptidase blocking cross link formation of peptidoglycan used for serious infections but not MRSA
|
carbapenems
|
|
inhibits dehydropeptidase, slowing degradation of imipenem (carbapenem)
|
cilastin
|
|
monobactam
|
aztreonam
|
|
inhibits transpeptidase blocking cross link formation of peptidoglycan
|
carbapenems
monobactams penicillin cephalosporins |
|
d-ala d-ala preventing binding of transpeptidase, used for MRSA, nephrotoxic, ototoxic, red man syndrome
|
vancomycin
|
|
inhibits dephosphorylation of C55 isoprentyl pyrophosphate carrier, blocks addition of UDP to lipid carrier
|
bacitracin
|
|
inhibits enol pyruvate transferase
|
fosfomycin
|
|
bind 23S RNA subunit of 50S ribosomal subunit
|
protein synthesis inhibitors
(streptogramins, oxazolidinones, macrolides, ketolides, lincosamides, chloramphenicol) |
|
streptogramins
|
quinupristin/dalfopristin
|
|
inhibit peptidyl transferase blocking elongation of peptide, used to treat VRE, MRSA, PRSP, SP
|
quinupristin/dalfopristin
|
|
inhibit transpeptidase-> inhibit synthesis of peptidoglycan
|
penicillin
Cephalosporins Carbapenems monobactams |
|
aminoglycosides used against P. aeruginosa
|
amikacin
gentamicin |
|
bind 16S to the 30S ribosomal subunit and prevent docking of tRNA on the ribosome
|
aminoglycosides
tetracyclines glycycycline |
|
competitively inhibit folic acid production by supressing the activity of dehydropteroate synthase
|
sulfonamides
|
|
inhibit dihydrofolate reductase
|
trimethoprim
|
|
block bacterial DNA synthesis (transcription and replication)
|
fluoroquinolones
|
|
Side effects: nephrotoxic, ototoxic
|
aminoglycosides
|
|
drug used for vaginitis
|
metronidazole
|
|
drug used topically for UTIs
|
mupirocin
|
|
used for UTI prophylaxis
|
methenamine
|
|
used for acute and chronic UTIs
|
nitrofurantoin
|
|
TB drug that can alter vision and should not be used in young children
|
ethambutol
|
|
drug that inhibits mycobacterial arabinosyl transferases
|
ethambutol
ethionamide (2nd line drug) |
|
most active TB drug, inhibits synthesis of mycolic acids
|
isoniazid
|
|
TB drug that can cause peripheral neuritis, hepatitis, CNS symptoms
|
isoniazid
|
|
drug that binds the B subunit of bacterial DNA dependent RNA polymerase inhibiting RNA synthesis
|
rifampin
|
|
drug that causes orange body fluids
|
rifampin
|
|
2nd line TB drug that inhibits folic acid synthesis (PABA analog)
|
aminosalicylic acid
|
|
drug that inhibits D-alanine ligase and racemase, causes psych and CNS changes
|
cycloserine
|
|
inhibits mycobacterial arabinosyl transferase and enhances the activity of lipophilic drugs
|
ethionamide
|
|
2nd line TB drugs
|
cycloserine
aminosalicylic acid ethionamide |
|
binds ergosterol in fungal cell membrane altering membrane permeability causing massive leakage of intracellular ions and macromolecules
|
polyenes: amphotercin B, nystatin
|
|
side effect of amphotercin B
|
nephrotoxic
|
|
targets beta 1,3 glucan synthesis which interferes with cell wall biosynthesis
|
echinocandins (caspofungin)
|
|
transported across the fungal cell membrane by cytosine permease and converted to 5FU, inhibits DNA and RNA synthesis, use with amphotercin B
|
flucytosine
|
|
Side effect of flucytosine
|
bone marrow suppression
|
|
binds mitotic spindle fibers inhibiting cell division incorporated into new keratin
|
griseofulvin
|
|
interferes with sterol biosynthesis by inhibiting the enzyme squalene 2,3 epoxidase decreasing the amount of ergosterol an causing squalene accumulation
|
terbinafine
|
|
Side effect of azoles
|
interfere with Cytochrome P450 metabolism
|
|
inhibit demtehylation of lamosterol causing ergosterol depletion
|
azoles (ketoconazole, itraconazole, fluconazole, voriconazole, posaconazole)
|
|
antifungal with excellent CNS penetration with the lowest Cytochrome P450 affinity
|
fluconazole
|
|
preferred antifungal for histoplasmosis and blastomyces
|
itraconazole
|
|
azole used for fluconazole resistance
|
voriconazole
|
|
side effect of voriconazole
|
visual disturbances
|
|
drug of choice for aspergillus
|
voriconazole
|
|
drug used to prevent invasive fungal infections in immunocompromised, glucuronidated, very lipophilic and penetrates CNS
|
posaconazole
|
|
converted to active triphosphate and competitively inhibit HIV reverse transcriptase and terminate viral DNA synthesis
|
nucleotide reverse transcriptase inhibitors
|
|
Side effects of NRTIs
|
bone marrow suppression
|
|
NRTI drug names
|
zidovudine
didanosine lamivudine emtricitabine stavudine abacavir |
|
NtRTI drug name
|
tenofovir
|
|
non-nucloside reverse transcriptase inhibitors drug names
|
nevirapine
efavirenz |
|
inhibit HIV RT by directly binding to the enzyme and altering the position of critical amino acids within the catalytic site preventing viral DNA synthesis
|
NNRTIs
|
|
SE of NNRTIs
|
lactic acidosis
|
|
inhibit viral enzyme responsible for maturation of viral proteins
|
protease inhibitors
|
|
class toxicity of protease inhibitors
|
lipodystrophy, inhibit Cytochrome P450
|
|
protease inhibitors drug names
|
ritonavir
fosamprenavir lopinavir/ritonavir atazanavir tipranavir darunavir |
|
36AA synthetic peptide that inhibits fusion of HIV virus to CD4 cell membrane receptor and blocks transfer of viral RNA into CD4 cell
|
fusion/entry inhibitors
|
|
fusion/entry inhibitors names
|
enfuvirtide
maraviroc |
|
drugs that target viral thymidine kinase that converts drugP->drugPPP and inhibits viral DNA polymerase
|
anti-herpetic agents
acylcovir famciclovir valacyclovir |
|
anti-herpetic agents
|
acyclovir
famciclovir valacyclovir |
|
anti-CMV agents
|
foscarnet
ganciclovir valganciclovir |
|
inhibits cleavage of pyrophosphate from deoxynucleotide triphosphate by inhibiting viral polymerase thus preventing the formation of the phosphate backbone of viral DNA
|
foscarnet
|
|
drugs used for HBV and HIV
|
lamivudine
tenofovir emtricitabine |
|
drugs against hepatitis C
|
pegylated interferon
ribavirin |
|
anti-influenza agents
|
oseltamivir
zanamivir |
|
viral neuraminidase inhibitors (enzyme responsible for releasing virus from infected cells)
|
oseltamivir, zanamivir (anti-influenza)
|
|
hep B drugs
|
pegylated interferon
lamivudine adefovir (like tenofovir) entecavir tenofovir emtricitabine |
|
ester local anesthetics
|
procaine
chloroprocaine tetracaine |
|
ester allergies due to
|
metabolism to PABA
|
|
max dose of procaine
|
1000mg
|
|
max dose of chloroprocaine
|
800-1000mg
|
|
epinephrines effect when used with local anesthetics
|
vasoconstrictor, prolongs duration
|
|
amide local anesthetics
|
lidocaine
prilocaine mepivacaine bupivacaine levobupivacaine etidocaine ropivacaine |
|
caution with local amide anesthetics
|
liver metabolized, caution in liver failure
|
|
max dose of lidocaine
|
4.5mg/kg or 300mg
7.5mg/kg or <500mg |
|
max dose of prilocaine
|
400mg within 2 hours
SE: methemoglobinemia |
|
mepivacaine
|
7mg/kg, <400mg
|
|
bupivacaine SE and max dose
|
cardiac toxicity
175 225mg w/epi 400mg |
|
levobupivocaine max dose
|
300mg
|
|
etidocaine max dose
|
4mg/kg or 300mg
5.5mg/kg or 400mg |
|
ropivacaine max dose
|
275mg
|
|
SE of halogenated hydrocarbons
|
dose dependent drop in BP
|
|
halogenated hydrocarbons
|
halothane
isoflurane enflurane sevoflurane desflurane |
|
halogenated hydrocarbon that is unstable in the presence of CO2 absorber
|
sevoflurane
|
|
short acting barbituate
|
thiopental
|
|
benzodiazepine example
|
midazolam
|
|
antagonist of benzodiazepines
|
flumazenil
(no antidote for barbituate thiopental) |
|
cause anterograde amnesia, "balanced amnesia"
|
midazolam
|
|
very commonly used IV agent for induction and maintenance of anesthesia, causes minimal postop confusion, antiemetic
|
propofol
|
|
used in patients at risk of hypotension, causes minimal cardiac and respiratory depression, inhibits steroidogenesis
|
etomidate
|
|
IV general anesthetic that causes dissociative anesthesia, emergence phenomenon, stimulates heart
|
ketamine
|
|
opioid that does not prolong labor
|
meperidine
|
|
anti-epileptic drugs
|
carbamazepine
oxcarbazepine ethosuximide gabapentin lamotrigine levetiracetam phenytoin fosphenytoin tiagabine topiramate valproic acid phenobarbitol benzodiazepines clonazepam diazepam lorazepam |
|
drug used for ataxia and cerebellar dysfunction, electrophysiologic evidence of peripheral neuropathy, causes gingival hyperplasia, osteomalacia
|
phenytoin
|
|
anti-epileptic used to treat peripheral neuropathy
|
gabapentin
|
|
block glutamic receptors, inhibit Ca currents, inhibit Na channels, potentiate GABA neurotransmission
|
anti-epileptic drugs
|
|
GABA neurotransmitter
|
inhibitory- target Cl
anti-anxiety sedative anti-epileptic |
|
Glutamate
|
excitatory
target NMDA and non-NMDA, ionotrophic, G protein coupled receptors, too much stimulation- neurotoxic anti-epileptic drugs anti-psychotic (investigational) neuroprotective agents |
|
glycine
|
inhibitor
target Cl channel co-transporter with glutamate glycine antagonists: convulsants |
|
acetylcholine
|
primary central nucleus in nucleus basalis of meynert
used to treat: parkinson's alzheimer's |
|
dopamine
|
D1: excitatory
D2: inhibitory treat: parkinson's schizophrenia emesis ADHD |
|
norepinephrine
|
acts on alpha and Beta receptors
tx: mood disorders narcolepsy obesity |
|
5 hydroxytriptamine
|
treat
anxiety mood disorders bulimia migraine emesis psychosis |
|
histamine
|
regulate arousal
body temperature vascular dynamics |
|
peptides
|
act with coexisting transporters
|