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Drug Study - Chole
Drug Study - Chole
PHARMACOLOGIC ACTION
INDICATIONS
SIDE EFFECTS
NURSING CONSIDERATIONS
Binds to mu-opioid receptors and inhibits the reuptake of norepinephrine and serotonin; causes many effects similar to the opioidsdizziness, somnolence, nausea, constipation, but does not have the respiratory depressant effects.
Relief of moderate to severe pain Relief of moderate to severe chronic pain in adults who need aroundthe-clock treatment for extended periods
Dizziness sedation drowsiness headache confusion dreaming sweating anxiety seizures hypotension tachycardia bradycardia pruritus rash pallor urticaria dry mouth constipation flatulence impaired visual acuity Nausea
Assess type, location, and intensity of pain before and 2-3 hr (peak) after administration. Assess BP & RR before and periodically during administration. Assess bowel function routinely. Assess previous analgesic history. Prolonged use may lead to physical and psychological dependence and
tolerance, although these may be milder than with opioids. Monitor patient for seizures. May occur within recommended dose range. Risk increased with higher doses and inpatients taking antidepressants, analgesics, or other drugs that decreses the seizure threshold. Overdose may cause respiratory depression and seizures. Encourage patient to cough and breathe deeply every 2 hr to prevent atelectasis and pneumonia.
PHARMACOLOGIC ACTION Anti-inflammatory and analgesic activity; inhibits prostaglandins and leukotriene synthesis
SIDE EFFECTS drowsiness abnormal thinking dizziness euphoria headache asthma dyspnea edema pallor vasodilation
NURSING CONSIDERATIONS Patients who have asthma, aspirininduced allergy, and nasal polyps are at increased risk for developing hypersensitivity reactions Assess pain prior to and 1-2 hr following administration. Ketorolac therapy should always be given initially by the IM or IV route. Oral therapy should be used only as a continuation of parenteral therapy. Caution patient to
GI Bleeding abnormal taste diarrhea dry mouth dyspepsia GI pain nausea oliguria renal toxicity urinary frequency pruritis purpura sweating urticaria prolonged bleeding
avoid concurrent use of alcohol, aspirin, NSAIDs, acetaminophen, or other OTC medications without consulting health care professional Advise patient to consult if rash, itching, visual disturbances, tinnitus, weight gain, edema, black stools, persistent headache, or influenza-like syndromes occur. Effectiveness of therapy can be demonstrated by decrease in severity of pain. Patients who do not respond to one NSAIDs may respond to another.
time
Histamine-2 antagonist
PHARMACOLOGIC ACTION Competitively inhibits the action of histamine at the H2 receptors of the parietal cells of the stomach, inhibits basal gastric secretion and gastric acid secretion that stimulated by food, insulin,
INDICATION
short term treatment of active duodenal ulcer maintenance therapy for duodenal ulcer at
SIDE EFFECTS Headache Malaise dizziness somnolence insomia vertigo tachycardia bradycardia rash
NURSING CONSIDERATIONS Assess patient for epigastric or abdominal pain and frank or occult blood in the stool, emesis, or gastric aspirate.
Nurse should
reduced dosage short term treatment and maintenance therapy of active, benign gastric ulcer Short term treatment of GERD Pathologic hypersecreto ry condition treatment of erosive esophagitis treatment for heartburn, acid indigestion, sour stomach
alopecia constipation diarrhea nausea vomitting abdominal pain hepatitis impotence or decrease libido local burning or itching on IV site
know that it may cause false-positive results for urine protein; test with sulfosalicylic acid.
Inform patient that it may cause drowsiness or dizziness Inform patient that increased fluid and fiber intake may minimize constipation. Advise patient to report onset of black, tarry stools; fever, sore throat; diarrhea; dizziness; rash; confusion; or hallucinations to health care professional promptly. Inform patient that medication may temporarily cause stools and tongue to appear gray
black.