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Drug Study 1
Drug Study 1
Drug Study 1
After:
Monitor patient's BP closely to evaluate effectiveness of therapy.
Monitor the patient in any situation that may lead to a drop in fluid
volume. Closely monitor patients who are taking diuretics.
Regularly assess patient's renal function (via creatinine and BUN levels).
Monitor patient response to the drug.
Monitor for adverse effects.
Document and record.
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DATE: January 10, 2023
After:
Monitor patient's response to the drug (relief of GI Symptoms caused by
hyperacidity, healing of erosive GI lesions).
Monitor the patient for signs and symptoms of low magnesium level,
such as abnormal HR and rhythm, palpitations, muscle spasms, tremors.
Periodically assess patient’s magnesium levels.
Monitor for adverse effects.
Document and record.
Generic Name: Tranexamic acid Tranexamic acid Contraindicated in Adverse effects include Before:
Tranexamic competitively and is indicated for patients hypersensitive seizures, headaches, Check doctor’s order.
Acid reversibly inhibits the the treatment of to drug or its backache, abdominal Ensure client’s identity. Use two patient identifiers at all times. Always
activation of significant components. pain, nausea, vomiting, follow agency policy for patient identification.
Dosage: plasminogen via bleeding in the Contraindicated to diarrhea, fatigue, Ensure medication has not expired.
500 mg PRN binding at several context of pulmonary embolism,
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DATE: January 10, 2023
distinct sites, including hyperfibrinolysis. patients with presence deep vein thrombosis, Ensure right dose and calculation of medication as well as right time.
Route: IV four or five low-affinity of blood clots (e.g., in anaphylaxis, impaired Explain to patient the purpose of medication administration.
sites and one high- the leg, lung, eye, color vision, and other Assess for contraindications, cautions and any known allergies.
affinity site, the latter brain), history or are at visual disturbances.
Therapeutic Assess baseline status, especially heart rate and rhythm.
of which is involved in risk for blood clots.
Class:
its binding to fibrin.
Antifibrinolytics During:
The binding of
plasminogen to fibrin Verify patient’s identity.
Pharmacologic induces fibrinolysis - Administer the right drug in the right dose and route at the right time.
Class: by occupying the Provide comfort measures and patient education about drug effects.
Cyclooxygenas necessary binding After:
e-2 inhibitors sites tranexamic acid Monitor patient's response to the drug. Monitor for manifestations of
prevents this adverse effects.
dissolution of fibrin, Monitor vital signs particularly the blood pressure and heart rate. Monitor
thereby stabilizing the
I&O.
clot and preventing
Monitor for adverse effects.
hemorrhage.
Document and record.
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