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Shejay Lomongo Final Exam BSN2
Shejay Lomongo Final Exam BSN2
Shejay Lomongo Final Exam BSN2
BSN - 2
Final Exam
A. Anti Inflammatory
162.5 mg
B. Anti Arthritis
75mg
(generic)
tablet,
extended-
release
100mg
(generic)
capsule
18mg
(Zorvolex)
35mg
(Zorvolex)
Warning
Epatient is well
hydrated
before
treatment to
reduce cystitis
Name of Date Classificati Dose/ Mechanism of Specific Contraindicati Side Nursing
drug Ordere on of Drug Frequency Action Indication on Effects Precaution
(Generic d
& Brand)
Mycophe Immunosu
nolate 7/27/20 ppressants capsule Inhibits T- Contraindicate Nausea, Warning
mofetil 00 lymphocyte Prophylaxis d with allergy vomiting; Monitor renal
250mg activation; of organ to diarrhea; and liver
GenNam exact rejction in mycophenolat headache function before
e: tablet mechanism of patients e, pregnancy, and
action recieving lactation periodically
BraNam 500mg unknown, but allogeneic during therapy;
e: binds to renal, hepatic marked
Cellcept oral intracellular and heart decreases in
suspension proteij, which transplants; function may
may prevent intended to require dosage
200mg/mL be used
the generation change or
of nuclear concomitantly discontinuation
powder for
factor of with of therapy.
injection
activated T corticosteroid
cells, and s and Black box
500mg/vial
suppresses the cyclosporine warning
immune Protect patient
tablet,
activation and from exposure
delayed
response of T to infections
release
cells; inhibits and maintain
180mg proliferative sterile
responses of t technique for
360mg and b cells invasive
procedures;
risk for
infection exists
Black box
warning
Monitor patient
for possible
lymphoma
development
related to drug
action
Name of Date Classificati Dose/ Mechanism of Specific Contraindicati Side Nursing
drug Ordere on of Drug Frequency Action Indication on Effects Precaution
(Generic d
& Brand)
Azathiop Immunosu
rine 20 ppressants tablet Suppressmedh Contraindicate Nausea Guve drug IV if
March ypersensetitviti Renal d with allergy and oral
GeName 1968 50mg es and alters homotranspla to vomiting adminustration
: antibody ntation: azathioprine; is not possible;
azathiop 75mg production; Adjunct for rheumatoid swticg to oral
rine exact prevention of arthritis route as soon
BraNam 100mg mechanisms of rejection patients as possible
e: action in previously
Azasan powder for Rheumatoid treated with Administer in
increasing
injection arthritis: Use alkylating divided daily
homograft
only with agents, doses or with
survival and
100mg/vial adults increasing food if GI
affecting
autoimmune
meeting theur risk for upset occurs
criteria for neoplasia;
disease not
classic pregnancy
clearly
rheumatoid
understood
artjritis and
not
responding to
conventional
management
Unlabeled
use
Treatment of
chronic
ulcerative
colitis
myasthenia
gravis,
Behcets
syndrome,
Crohn's
disease,
clinically
definite MS
D. Immune stimulant
Name of Date Classificati Dose/ Mechanism of Specific Contraindicati Side Nursing
drug Ordere on of Drug Frequency Action Indication on Effects Precaution
(Generic d
& Brand)
GenNam Solid
e: DMARDs Organ Calcineurin Hypersensitivit Injection:
Cyclosp Transplan inhibitor For the y monitor closely
orine Immunomo tation prophylaxis for at least 30
dulators; of organ Breastfeeding min
(Oral):
BraNam Immunosu rejection in
4-12 hr Suppresses
e: ppressants kidney, (RA/Psoriasis
; pre- cellular and use):
Neoral, liver, and
Sandim Calcineurin transplant: humoral Abnormal Risk of
15 mg/kg heart hepatotoxicity
Inhibitors immunity renal function,
mune, PO for 1 allogeneic and
(mainly T cells) uncontrolled
Gengraf dose transplants. nephrotoxicity
HTN,
1-2wk It is always malignancies
post- to be used
transplant: with adrenal (Psoriasis
Myelosuppres
15 corticosteroi use)
Concomitant sion may be
mg/kg/da ds. The drug
PUVA, UVB severe and
y PO may also be
radiation, coal prolonged;
divided used in the
tar, monitor
BID treatment of complete
methotrexate,
>Psoriasis chronic blood and
other
: rejection in immunosuppr platelet counts
1.25 patients essants
mg/kg PO previously
BID; may treated with
other Potential
increase increase risk
by 0.5 immunosup
for optic disk
mg/kg/da pressive
edema and
y agents.
infusion-
related
>Monitor anaphylactic
for signs reactions
and
symptoms
of infection;
severe and Some
fatal sepsis malignancies
caused by
as a result of
cyclosporine
bone
immunosuppre
marrow
ssion may be
suppression;
fatal (eg,
discontinue lymphoma)
if observed.
Serious and
fatal cerebral,
gastrointestina
l and
pulmonary
hemorrhage;
monitor
platelets and
coagulation
parameters
and treat
accordingly
Anticipate and
monitor for
signs and
symptoms of
tumor lysis
syndrome
occur; treat
promptly
Monitor for
and
discontinue
promptly if
systemic
inflammatory
response or
capillary leak
syndrome
suspected
Monitor for
signs and
symptoms of
infection;
severe and
fatal sepsis as
a result of
bone marrow
suppression;
discontinue
therapy
promptly if
infection occur
Monitor for
and
discontinue if
venous
occlusive
disease of the
liver suspected
Monitor liver
enzymes and
discontinue
therapy at first
signs of
severe
hepatotoxicity;
fatal
hepatotoxicity
may occur
Monitor renal
function and
interrupt or
discontinue if
creatinine
levels increase
or acute renal
failure occur
Acute
treatment of
herpes zoster
and chicken
pox
Name of Date Classificati Dose/ Mechanism of Specific Contraindicati Side Nursing
drug Ordere on of Drug Frequency Action Indication on Effects Precaution
(Generic d
& Brand)
Atropine Anticholine
eye drop 07/09/2 rgic intramuscul Competitively Contraindicate Dizziness, Ensure
001 ar device blocks the Systemic d with confusion; adequate
GenNam Antidote effects of administrati hypersentivity dry mouth; hydration;
e: 0.25mg/ acetylcholine at on to blurred provide
atropine Antimuscar 0.3mL muscarinic anticholinergic vission, environmental
inic Antisialagogu drugs
cholinergic sensitivity control to
BraNam 0.5mg/ e for
receptors that to light; prevent
e: Antiparkiso 0.7mL preanesthetic
mediate the impotence; hyperpyrexia
AtroPen nian medication to
effect of difficultt in
1mg/0.7mL prevent or Have patient
parasympatheti urination
Belladonna reduce void before
c
alkaloid 2mg/0.7mL postganglionic
respiratiry taking
tract medication if
impulses,
Diagnostic injectable secretions urinary
depressing
agent solution retension is
salivary and Treatment of
(ophthalmi problem
bronchial parkinsonism
c 0.05mg/mL
secretions,
preparatio ; relieves
ns) 0.1mg/mL dilating the tremor and
bronchi, regidity
Parasymp 0.4mg/mL inhibiting vagal
atholytic influences on Restoration
0.8mg/mL the heart l, of cardiac
relaxing the GI rate and
1mg/mL and GU tracts, arterial
pressure
during
anesthesia
when vagal
stimulation
prodyced by
intra-
abdominal
traction
causes a
decrease in
pulse rate
Relief of
bradycardia
and syncope
due to
hyperactive
carotid sinus
reflex
Antidote
Ophthalmic
prepartions
Diagnosticall
y to produce
mydriasis
and
cyxlopegia-
pupillary
dilation in a
cute in-
flammatiry
conditions of
the iris and
uveal tract
Dosage
adjustments
may be
necessary if
CrCl is <30
mL/min
Bacterial or
fungal
overgrowth of
nonsusceptible
organisms
may occur with
prolonged or
repeated
therapy
Use caution in
patients with
history of
colitis
Antacids
containing
magnesium or
aluminum
interfere with
absorption of
cefdinir; if this
required
during therapy,
administer at
least 2 hr
before or after
antacid
Iron
supplements,
including
multivitamins
that contain
iron, interfere
with
absorption of
cefdinir; if iron
supplements
required
administer at
least 2 hours
before or after
supplement
Chewable
tablets contain
aspartame,
which contains
phenylalanine
Use caution in
patients with
allergy to
cephalosporin
s,
carbapenems
Endocarditis
prophylaxis:
use for only
high-risk
patients, as
per recent
AHA
guidelines
High doses
may cause
false urine
glucose test by
some
methodso
Prolonged
treatment,
hepatic or
renal disease,
or nutritional
deficiency may
be associated
with increased
international
normalized
ratio (INR)
Prolonged use
is associated
with fungal or
bacterial
superinfection
Use with
caution in
patients with
history of
hypersensitivit
y to penicillin
5. Vaccines
N/V
Cautions
Polysaccharid
Lymphade e capsular
nitis vaccine
against 23
strains of
pneumococci
ITP (90% of blood
relapse isolates & 85%
of isolates
found in sterile
sites)
Hemolytic
anemia
CDC now
recommends
Thromboc second dose
ytopenia after 5 years
for pts with
chronic renal
failure,
Anaphylac asplenia, HIV
toid infection,
reaction cancer, or
other
conditions
associated
Angioede w/immunosup
ma pression
Serum Splenectomy:
sickness administer at
due to least 2 wk
drug before
scheduled
procedure
Guillain-
Barre
syndrome
Defer
vaccination in
persons with
moderate or
severe acute
illness
Exercise
caution and
appropriate
care in
individuals
with severely
compromised
cardiovascular
and/or
pulmonary
function in
whom a
systemic
reaction would
pose
significant risk
This vaccine
does not
replace the
need for
penicillin (or
other
antibiotic)
prophylaxis
against
pneumococcal
infection. In
patients who
require
penicillin (or
other
antibiotic)
prophylaxis
against3
Vaccine does
not replace
need for
penicillin (or
other
antibiotic)
prophylaxis
against
pneumococcal
infection; in
patients who
require
penicillin (or
other
antibiotic)
prophylaxis
against
neumococcal
infection, such
prophylaxis
should not be
discontinued
after
vaccination
Persons who
are
immunocompr
omised,
including
persons
receiving
immunosuppre
ssive therapy,
may have a
diminished
immune
response to
vaccine
Vaccine may
not be
effective in
preventing
pneumococcal
meningitis in
patients who
have chronic
cerebrospinal
fluid (CSF)
leakage
resulting from
congenital
lesions, skull
fractures, or
neurosurgical
procedures
Syncope
reported;
procedures
should be in
place to avoid
injury from
fainting
Reduced
immune
response may
occur in
immunosuppre
ssed
individuals
Persons with
certain
complement
deficiencies
and persons
receiving
treatment that
inhibits
terminal
complement
activation (eg,
eculizumab)
are at
increased risk
for invasive
disease
caused by N
meningitidis
serogroup B
even if they
develop
antibodies
following
vaccination
Sufficient data
are not
available on
the safety and
effectiveness
of
interchanging
meningococcal
group B
vaccines to
complete the
vaccination
series
Bexsero: The
tip caps of the
prefilled
syringes
contain natural
rubber latex
which may
cause allergic
reactions in
latex sensitive
individuals
(Trumenba's
caps are not
made with
natural rubber
latex)
Name of Date Classificati Dose/ Mechanism of Specific Contraindicati Side Nursing
drug Ordere on of Drug Frequency Action Indication on Effects Precaution
(Generic d
& Brand)
Flu Vaccines
vaccine Novem IM Mechanism of Hypersensitivit injection Use split or
ber Inactivated injection, Action is a vaccine y to eggs, site purified
GenNam 2015 regular indicated for sulfites reactions surface
e: Flu Viral strength Inactivated active (persons with antigen in
chills,
vaccine influenza virus immunization hives-only children
joint or
22.5mcg/ types A & B for the allergy to muscle
BraNam 0.25mL subunits prevention of eggs, can aches or
e:Afluria, influenza receive the pain,
Fluzone 45mcg/ disease inactivated Defer vaccine
headache
0.5mL caused by influenza with febrile
,
Convey active influenza A vaccine) illnesses until
tired
ID injection immunity via subtype feeling, illness is
stimulation of viruses and weakness resolved; may
27mcg/ production of type B virus , or. administer
0.1mL endogenously contained in fussiness vaccine with
(Fluzone produced the vaccine. or crying minor illnesses
Intradermal antibodies in without fever
) children. (eg, URIs)
Expected
immune
response may
not be
obtained in
immunocompr
omised
individuals,
including those
receiving
immunosuppre
ssive therapy
Syncope
(fainting) can
occur in
association
with
administration
of injectable
vaccines; can
be
accompanied
by transient
neurological
signs such as
visual
disturbance,
paresthesia,
and tonic-
clonic limb
movements;
procedures
should be in
place to avoid
falling injury
and to restore
cerebral
perfusion
following
syncope by
maintaining a
supine or
Trendelenburg
position
Vaccination
may not
protect all
vaccine
recipients
against
influenza
disease
6. Immunization
Avoid
pregnancy for
3 months
following
therapy
Avoid taking
salicylates for
6 weeks after
vaccination
(may increase
risk of Reye's
syndrome
Lymphade
nopathy
Myalgia