Cross-sensitivity may exist with other NSAIDs, including aspirin, dehydration, or patients on nephrotoxic drugs (may risk of renal toxicity) not recommended for pregnant patients; has been associated with persistent pulmonary hypertension in infants, has been used safely during lactation.
Cross-sensitivity may exist with other NSAIDs, including aspirin, dehydration, or patients on nephrotoxic drugs (may risk of renal toxicity) not recommended for pregnant patients; has been associated with persistent pulmonary hypertension in infants, has been used safely during lactation.
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Cross-sensitivity may exist with other NSAIDs, including aspirin, dehydration, or patients on nephrotoxic drugs (may risk of renal toxicity) not recommended for pregnant patients; has been associated with persistent pulmonary hypertension in infants, has been used safely during lactation.
Copyright:
Attribution Non-Commercial (BY-NC)
Available Formats
Download as DOC, PDF, TXT or read online from Scribd
NURS 1566 Clinical Form 3: Clinical Medications Worksheets
(You will need to make additional copies of these forms)
Generic Name Trade Name Classification Dose Route Time/frequency
ibuprofen Advil, Motrin IB nonopioid 800 mg PO t.i.d (taken with food) analgesics, NSAID Peak Onset Duration Normal dosage range 1-2 hr 30 min 4-6 hr Why is your patient getting this medication For IV meds, compatibility with IV drips and/or Mild to moderate pain, postpartum/post-op pain solutions N/A Mechanism of action and indications Nursing Implications (what to focus on) (Why med ordered) Contraindications/warnings/interactions Inhibits prostaglandin synthesis Hypersensitivity. Cross-sensitivity may exist with other NSAIDs, including aspirin, dehydration, or patients on nephrotoxic drugs (may ↑ risk of renal toxicity). Not recommended for pregnant patients; has been associated with persistent pulmonary hypertension in infants, has been used safely during lactation. Common side effects Headache, constipation, dyspepsia, nausea, vomiting, GI BLEEDING, HEPATITIS, EXFOLIATIVE DERMATITIS, STEVENS-JOHNSON SYNDROME, TOXIC EPIDERMAL NECROLYSIS, ALLERGIC REACTIONS INCLUDING ANAPHYLAXIS Interactions with other patient drugs, OTC or Lab value alterations caused by medicine herbal medicines (ask patient specifically) Serum potassium, BUN, serum creatinine, alkaline phosphatase, LDH, AST, and ALT may show ↑ levels. Blood glucose, hemoglobin, and hematocrit concentrations, leukocyte and platelet counts, and CCr may be ↓ Be sure to teach the patient the following about this medication For rapid initial effect, administer 30 min before or 2 hr after meals. May be administered with food, milk, or antacids to decrease GI irritation. Tablets may be crushed and mixed with fluids or food. May cause drowsiness or dizziness. Advise patient to avoid driving or other activities requiring alertness until response to medication is known. Advise patient to consult health care professional if rash, itching, visual disturbances, tinnitus, weight gain, edema, black stools, persistent headache, or influenza-like syndrome (chills, fever, muscle aches, pain) occurs. Nursing Process- Assessment Assessment Evaluation (Pre-administration assessment) Why would you hold or not give this Check after giving Assess for rhinitis, asthma, and urticaria med? Decrease in severity of pain. Assess pain (note type, location, and If pain has subsided, dangerous or intensity) prior to and 1-2 hr following undesirable side effects occur. administration.