M.I. (Losartan) Drug Study)
M.I. (Losartan) Drug Study)
Patient’s Initial: _______M.I.______________ Age: ___49__________ Date of Birth: ______12/19/1973_____ Gender: _____MALE__________
Chief Complaint: ________Hypogastric Pain _______ Medical Diagnosis: _______T/C Nephrolithiasis, HTN stage II______________ Room/Bed #: ____328-B______
Submitted by: ____________________________________ Section/Group #: _________ Submitted to: _____________________ Hospital/Area: ______________ Date: ___________
achieved in about • may cause hypotension,
1 hour after an tacycardia, angiodema,
oral dose. It is hyperkalemia
98% bound to • may increase digoxin
plasma protein. It levels
is excreted in Adverse Effect: • assess blood pressure
urine and in feces Adverse effects have and heart rate
as unchanged drug been reported to be • assess fluid levels
and metabolites. usually mild and • monitor daily weights
Following oral transient in nature. with CHF
dose, about 4% of The most common • monitor renal and liver
the dose is drug-related side • instruct patient on how
excreted effects were to take blood pressure
unchanged in dizziness, After:
urine and about asthenia/fatigue, and Notify physician of
6% in urine as the vertigo. The overall symptoms of
active metabolite. incidence of side hypotension (e.g.,
effects reported with dizziness, fainting).
Losartan potassium Notify physician
was comparable to immediately of
placebo. pregnancy.
View Do not breast feed while
taking this drug
Submitted by: ____________________________________ Section/Group #: _________ Submitted to: _____________________ Hospital/Area: ______________ Date: ___________