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the acronym for protease inhibitors is
FRTND (friend)
the prototype for protease inhibitors are
fosamprenavir
the protease inhibitor fosamprenavir works by
inhibiting protease, causing immature particles
fosamprenavir is specifically used for
symptomatic HIV only
the second protease inhibitor is
ritonavir
ritonavir is specifically a combo drug that can have
toxic effect when taken with non sedating enzymes, antihistamines, hypnotics, antiarrythmics
the third protease inhibitor is
tipranavir
tipranavir must be given with
high doses of ritonavir
food
the usage of tipranavir can lead to
toxic liver dysfunction
the fourth protease inhibitor is
nelfinavir
the protease inhibitor nelfinavir is (good) and can be taken in patients who have
renal impairments
the final protease inhibitor is
darvunavir
the protease inhibitor darunavir is known for causing
hyperglycemia
DM
steven johnson syndrome
it is critcal that all protease inhibitors are not taken with
grapefruit jucie
seizure meds
st.john wort
protease inhibitors cause an increase in
triglycerides
cholesterol
that can lead to a redistribution of body fat
all protease inhibitors can be used in
both adults and children
protease inhibitors can not be taken in patients who have
DM
all protease inhibitors can lead to
steven johnson syndrome
the general purpose of all protease inhibitors is to
prevent maturation of diseased cells
the prototype and only fusion drug is
enfuvirtide
enfuvurtide works by
preventing HIV entry into cells and inhibiting membrane fusion
enfuvirtide should only be used if
other HIV and AIDs treatments have failed
enfuvirtide can cause patients to have
pnumonia
chills
one odd fact regarding enfuvirtide is that it is
not excreted at all
along side it being a last resort treatment enfuvirtide should only be given if the patient is
having evident viral replication
if a patinet is taking enfuvirtide they may expereice
insomnia
depression
peripheral neuropathy
the one and only CCR5 drug is
maraviroc
the CCR5 inhibitor maraviroc works by
preventing the interaction between CCR5 and HIV1
one specific thing about the mechanism of CCR5 is that it
cannot enter the cell or multiply
the CCR5 medication maraviroc is used for people who are
evident of viral replication and HIV 1 strains that are resisitant to all other antiretroviral agents
maraviroc can cause a patient to expereice
paresthesia
URI/ fever/ cough
muskuloskeletal symptoms
maraviroc can lead to severe
hepato toxicity
there is a severe increase in toxicity with maraviroc when taking
keto
rito
saquin
ata
dela
maraviroc cannot be taken if
breast feeding
usage of st. john wort
coinfection HBV cardio events
if a patient has a coinfection of HBV they cannot also take CCR5s or they will expereicne
cardiac events
CCR5s are used in
adults only
CCR5s are excreted in the
feces