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pharmacokinetics
the study of what the BODY does to the drug
pharmacodynamics
the study of what the DRUG does to the body
First pass effect-
the drug being metabolized by the liver
bioavailablility
the amount of the drug that is actually available after being metabolized
protein binding
drug needing to bind to protein inorder to move through out the body
peak
the time it takes for the drug to reach its maximum therapeutic response
onset
the time it takes for the drug to elicit a therapeutic response
duration
the time a drug concentration is sufficient to elicit a therapeutic response without giving additional doses
half life
the time it takes for one half of the original amount of drug to leave the body(measure of rate fo the drug leaving the body)
therapeutic index
lethal dose divided by therapeutic dose
trough
lowest blood level
peak level
highest blood level
agonist
drug binds to the receptor and there is a response
antagonist
drug binds to the receptor but there is no response,
*antagonist prevent agonist to bind to receptors(attach but dont activate)
acute therapy
examples: allergic reaction, someone who is coding
maintenance therapy
wont cure but it will prevent complications
ex) BP meds, insulin
supplemental therapy
hormones, vitamins, insulin
palliative therapy
providing utmost comfort for patient near death
supportive therapy
maintains the integrity of body functions while the patient is recovering from illness or trauma.
ex) provision of fluid while electrolytes to prevent dehydration in a patient with influenza who is vomiting and has diarrhea, and administration of fluids, volume expanders, or blood products to a patient who has lost blood during surgery
prophylactic therapy
prevention
empiric therapy
based on clinical probabilities. it involves drug administration when a certain pathologic condition has an uncertain but high likelihood of occurrence based on patients initial presenting symptoms.
ex)common: use of antibiotics active against the organism most commonly associated with a specific infection before the results of the culture and sensitivity reports are available
additive effect
combining 2 meds to reduce the dosage of another
synergistic effect
drug interactions that make the effect of a combination of drugs similar actions greater than just one
antagonistic
a drug that binds to and inhibits the activity of 1 or more receptors in the body.
AKA inhibitors
incompatibility
the characteristic that causes two parenteral drugs or solutions to undergo a reaction when mixed or given together that results in the chemical deterioration of at least one of the drugs
macrolides "thromycin"
prevent protein synthesis within bacterial cells
both bacteriostatic and bactericidal
"thromycin" indication
strep infections
mild-moderate URI and LRI
syphilis and lyme disease, gonorrhea, chlamydia, mycoplasma,
clarithromycin combination with omeprazole: active ulcer disease associated with H.pylori
"thromycin" adverse effects
GI effects, primarily with erythromycin
N/V, diarrhea, hepatotoxicity, flatulence, jaundice, anorexia
azithromycin and clarithromycin: fewer GI adverse effects, longer duration of action, better efficacy, better tissue penetration
"thromycin" nursing implications
highly protein bound: severe interactions with other protein bound drugs
high incidence of GI upset, many drugs are taken after a meal or snack
"cyclines"
bacteriostatic
bind to Ca+ and Mg+ and Al+ ions to form insoluble complexes
*dairy products, antacids, and iron salts reduce oral absorption
"cycline" indications
wide spectrum
gram- and gram+, protozoa, mycoplasma, rickettsia, chlamydia, lyme disease,acne, others
"cycline" adverse effects
strong affinity to calcium
discoloration of teeth and tooth eneamel in fetus and children. or nursing infants
may retard skeletal development if taken during pregnancy
alterations in intestinal flora may result in:
superinfection, diarrhea, pseudomembranous colitis, vaginal candidiasis, gastric upset, enterocolitis, maculopapular rash
"cycline" nurisng implications
avoid milk products, iron prep, antacids bc of the chelation and drug-binding that occurs
take all meds with 6-8 oz of fluid- prefer water
bc of photosensitivity, avoid sunlight and tanning beds
aminoglycosides:Gentamycin
poor oral absorptin, no PO forms (except neomycin)
very potet antibiotics with serious toxicities
bactericidal; prevent protein synthesis
kill mostly gram- bacteria; some gram+
aminoglycosides indications
used to kill ecoli, proteus spp, klebsiella, serratia
poorly absorbed through GI, given parenterally
aminoglycosides: adverse effects
serious: nephrotoxicity and ototoxicity
must monitor drug levels to prevent toxicity
minimum inhibitory concentration
others: headache, paresthesia, fever, superinfection, vertigo, skin rash, dizziness
quinolones "floxacin"
AKA flouroquinolones
excellent oral absorption
absorption reduced by antacids
bactericidal
"floxacin" indications
complicated urinary tract, respiratory, bone and joint, GI, skin and sexually transmitted infections
"floxacin" adverse effects
insomnia, depression, convulsions
thrush, increased liver function studies
prolonged QT intervals
rash, urticaria, flushing
fever, chills, blurred vision, tinnitus
**BLACK BOX WARNING: increased risk of tendonitis and tendon rupture**
vancomysin (vancocin)
treatment of choice for MRSA
oral vancomysin- antibiotic-induced colitis (cdiff) and fro treatment of staph. enterocolitis
may cause ototoxicity adn nephrotoxicity
MUST MONITOR BLOOD LEVELS TO ENSURE THERAPEUTIC LEVELS AND PREVENT TOXICITY
toxic level: > 20 mcg/ml(trough)
redmans syndrom(flushing/itcihng of head, neck,face and upper trunk, antihistamine may be orders to reduse those effects) and hypotension are common with rapid infusion
clinaycin(cleocin)
used for chronic bone infections, GU infections
**FDA BLACK BOX WARNING: cdiff associated diarrhea**
metronidazole (flagyy)
used for anaerobic organisms, protozoal infections
contraindications: alcohol use within 3 days , pregnancy 1st
trimester
*avoid alcohol 24 hours before first dose and 36 hours after last dose*
nitrofurantonin (microdantin)
primarily used for UTIs
drug concentrates in the urine, use carefully if renal function is impaired
may cause fatal hepatotoxicity
antiviral (non HIV)
used to treat infections cause by viruses other than HIV
influenza
HSV, VZV
CMV
hepatitis A,B,C
antiretroviral drugs
used to treat infections caused by HIV, the virus that causes AIDS
inhibit viral replication
antiretroviral adverse effects
vary with each drug
healthy cells are often killed also, resulting in serious toxicities
acyclovir(zovirax)
used to suppress replications of HSV 1,2, VZV
drug of choice for treatment of initial and recurrent episodes of these infections
oral, topical, parenteral forms
ganciclovir (cyovene)
used to treat infection with cytomegalovirus(CMV)
oral and parenteral forms
CMV retinitis
opthalmic form surgically implanted(vitrasert)
bone marrow toxicity
oseltamivir (tamiflu)
zannamivir (relenza)
active against influenza A and B
reduce duration of illness
oseltamivir: causes N/V
zannamivir: causes diarrhea, nausea and sinusitis
treatment should begin within 2 days of influenza symptoms onset
chemotherapy
treatment of cancer
antineoplastic drugs
2 groups: CCNS &CCS(some drugs have characteristics of both)
narrow therapeutic therapy index
drug resistance
combination of drugs
harmful to rapidly growing cells
*harmful cancer cells
*healthy normal human cells
**hair follicles
**GI tract cells
**bone marrow cells
Chemo terms
dose limiting adverse effects
*GI tract and bone marrow
alopecia
emetic potential
myelosuppression
*BMS
*BMD
targeted drug therapy
nadir
lowest amount of WBC
common with chemo
extravastion
burning from inside out due to chemotherapy
***nursing implications
chemotherapy
baseline CBC
follow specific admin guidelines
remember all rapidly dividing cells(normal and cancerous) are affected
*mucous membranes
*hair follicles
*bone marrow components
monitor for and prevent: infection, bleeding,
Anemia
may result if SEVERE fatigue
antiretrovirus'
opportunistic infections
HIV and AIDs
protozoal, fungal, viral: CMS disease, HSV infections, bacterial-opportunistic neoplasias
HIV wasting syndrome
major weight loss,, chronic diarrhea, chronic fever
antiretroviral drugs HAART
includes at least 3 meds "cocktails"
all meds work in different ways to reduce the viral load
goal: find the regimen that will best control the infection with a tolerable adverse effect profile
med regimens charge during the course of illness
zidovudine
antiretroviral
given to HIV- infected pregnant women and new born babies to prevent maternal transmission
dose limited adverse effect: bone marrow suppression
other examples of antiretroviral
enfuvirtide(fuzeon)
indinavir(crixivan)
maraviroc (selzentry)
nevirapine(viramune)
raltegravir(isentress)
tenofovir(viread)
isoniazid(INH)
antitubercular
metabolized in the liver through acetylation- watch for "slow acetylators"
used alone or in combination with other drugs
contraindicated with liver disease
used for the prophylaxis and treatment of TB
***peripheral neuropathy- pyridoxine
***hepatotoxicity
rifampin
antiTB
red-orange discoloration of body fluids
MDR/MDX-TB
prevention of MDR-TB
amphotericin B
antifungal-systemic infections
aphotericin B adverse effects
cardiac dysrhythmias
neurotoxicity,tinnitus, visual disturbances, hand or feet numbness, tingling or pain, convulsions
renal toxicity, potassium loss, hypomagnesemia
pulmonary inflitrates
fever, chills, headache, hypotension, GI upset, anemia
fluconazole
N/V diarrhea, stomach pain
increased liver enzymes
use with caution in patients with renal and liver dysfunction
-azoles
imidazoles and triazoles: ketoconazole, fluconazole, itraconazole, voriconazole,
inhibit fungal cell cytochrome p-450 enzymes, resulting in cell membrrane leaking
results:altered cellular metabolism and fungal cell
nystatin
N/V anorexia, diarrhea, rash
needs to be dissolved slowly and steady
cisplatin(pantinol)
alkylating drugs
alter the chemical structure of the cells DNA
alkylating drugs
adverse effects
gi tract, myelosuppression, alopecia
nephrotoxiciy, peripheral neuropathy, ototoxicity,
*hydration can prevent nephrotoxicity
cyclophosphamide(cytoxan)- hemorrhagic cystitis
extravasation causes tissue damage and necrosis
cytotoxic antibiotics (doxorubicin)
natural substance produced by the mold streptomyces
active in all phases of cell cycle, blockade of DNA
EX) daunorubicin, bleomycin
cytotoxic antibiotics
adverse effects
all can produce done marrow suppression, except bleomycin
hair loss, N/V
pulmonary fibrosis and pneumonitis(bleomycin)
liver, kidney and cardiovascular toxicities
heart failure- cardiomyopathy(daunorubicin)