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Carboprost tromethamine stimulates the myometrium of the pregnant uterus to contract. Midazolam hydrochloride is a benzodiazepine (short-acting); CNS depressant. Contraindications: - Contraindicated with allergy to prostaglandin preparations, acute PID; active cardiac,hepatic,pulmonary, renal disease.
Carboprost tromethamine stimulates the myometrium of the pregnant uterus to contract. Midazolam hydrochloride is a benzodiazepine (short-acting); CNS depressant. Contraindications: - Contraindicated with allergy to prostaglandin preparations, acute PID; active cardiac,hepatic,pulmonary, renal disease.
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Carboprost tromethamine stimulates the myometrium of the pregnant uterus to contract. Midazolam hydrochloride is a benzodiazepine (short-acting); CNS depressant. Contraindications: - Contraindicated with allergy to prostaglandin preparations, acute PID; active cardiac,hepatic,pulmonary, renal disease.
Copyright:
Attribution Non-Commercial (BY-NC)
Formatos disponibles
Descargue como ODT, PDF, TXT o lea en línea desde Scribd
Brand Name: Hemabate Classification: Prostaglandin; Abortifacient Therapeutic Actions: • Stimulates the myometrium of the pregnant uterus to contract; similar to the contractions of the uterus during labor, thus evacuating the contents of the uterus. Indications: - Termination of pregnancy 13-20 wk from the first day of the LMP - Evacuation of the uterus in instance of missed abortion or intrauterine fetal death in the 2nd trimester - Postpartum hemorrhage due to uterine atony unresponsive to conventional methods Contraindications: - Contraindicated with allergy to prostaglandin preparations, acute PID; active cardiac,hepatic, pulmonary, renal disease Adverse Effects: CNS: headache, paersthesias, flushing, anxiety, weakness, syncope, dizziness CV: hypotension, arrhythmias, chest pain GI: vomiting, diarrhes, nausea Nursing Considerations: - Assess allergy to the drug - Monitor uterine tone and vaginal discharge during procedure and several days after to assess drug effects and recovery - Ensure adequate hydration
Generic Name: Midazolam hydrochloride
Brand Name: Versed Classification: Benzodiazepine (short-acting); CNS depressant Therapeutic actions: - Exact mechanisms of action not understood; acts mainly at the limbic system and reticular formation; potentiates the effects of GABA, an inhibitory neurotransmitter; anxiolytic and amnesia effects occur at doses below those needed to cause sedation, ataxia; has little effect on cortical function. Indications - IV or IM: Sedation, anxiolysis, and amnesia prior to diagnostic, therapeutic, or endoscopic procedures or surgery - Induction of general anesthesia - Continuous sedation of intubated and mechanically ventilated patients as a component of anesthesia or during treatment in the critical care setting - Unlabeled uses: Treatment of epileptic seizure or refractory status epilepticus
Contraindications and cautions
- Contraindicated with hypersensitivity to benzodiazepines; psychoses, acute narrow-angle glaucoma, shock, coma, acute alcoholic intoxication; pregnancy (cleft lip or palate, inguinal hernia, cardiac defects, microcephaly, pyloric stenosis have been reported when used in first trimester; neonatal withdrawal syndrome reported in infants); neonates. - Use cautiously in elderly or debilitated patients; with impaired liver or kidney function, lactation. Adverse effects CNS: Transient, mild drowsiness (initially); sedation, depression, lethargy, apathy, fatigue, light-headedness, disorientation, restlessness, confusion, crying, delirium, headache, slurred speech, dysarthria, stupor, rigidity, tremor, dystonia, vertigo, euphoria, nervousness, difficulty in concentration, vivid dreams, psychomotor retardation, extrapyramidal symptoms; mild paradoxical excitatory reactions (during first 2 wk of treatment), visual and auditory disturbances, diplopia, nystagmus, depressed hearing, nasal congestion CV: Bradycardia, tachycardia, CV collapse, hypertension, hypotension, palpitations, edema Dermatologic: Urticaria, pruritus, skin rash, dermatitis GI: Constipation, diarrhea, dry mouth, salivation, nausea, anorexia, vomiting, difficulty in swallowing, gastric disorders, elevations of blood enzymes: LDH, alkaline phosphatase, AST, ALT, hepatic dysfunction, jaundice GU: Incontinence, urinary retention, changes in libido, menstrual irregularities Hematologic: Decreased Hct, blood dyscrasias Other: Phlebitis and thrombosis at IV injection sites, hiccups, fever, diaphoresis, paresthesias, muscular disturbances, gynecomastia; pain, burning, and redness after IM injection Dependence: Drug dependence with withdrawal syndrome when drug is discontinued (more common with abrupt discontinuation of higher dosage used for longer than 4 mo)
Nursing considerations
- History: Hypersensitivity to benzodiazepines; psychoses, acute
narrow-angle glaucoma, shock, coma, acute alcoholic intoxication with depression of vital signs; elderly or debilitated patients; impaired liver or kidney function; pregnancy, lactation - Physical: Weight; skin color, lesions; orientation, affect, reflexes, sensory nerve function, ophthalmologic examination; P, BP; respiratory rate, adventitious sounds; bowel sounds, normal output, liver evaluation; normal output; LFTs, renal function tests, CBC - Do not administer intra-arterially, which may produce arteriospasm or gangrene. - Do not use small veins (dorsum of hand or wrist) for IV injection. - Administer IM injections deep into muscle. - Arrange to reduce dose of midazolam if patient is also being given opioid analgesics; reduce dosage by at least 50% and monitor patient closely. - Monitor level of consciousness before, during, and for at least 2–6 hr after administration of midazolam. - Carefully monitor P, BP, and respirations carefully during administration. - Keep resuscitative facilities readily available; have flumazenil available as antidote if overdose should occur. - Keep patients in bed for 3 hr; do not permit ambulatory patients to operate a vehicle following an injection. - Establish safety precautions if CNS changes occur (use side rails, accompany ambulating patient). - Client may experience these side effects: Drowsiness, dizziness (these may become less pronounced after a few days; avoid driving a car or engaging in other dangerous activities if these occur); GI upset; dreams, difficulty concentrating, fatigue, nervousness, crying (it may help to know that these are effects of the drug; consult your health care provider if these become bothersome). - Report severe dizziness, weakness, drowsiness that persists, rash or skin lesions, visual or hearing disturbances, difficulty voiding.
Generic Name: Hyoscine-N-butylbromide
Brand Name: Buscopan Classification: Antispasmodic; Anticholinergic Therapeutic Actions: - acts by interfering with the transmission of nerve impulses by acetylcholine in the parasympathetic nervous system. Indications: - Buscopan Tablets are indicated for the relief of spasm of the genito- urinary tract or gastro- intestinal tract and for the symptomatic relief of Irritable Bowel Syndrome Contraindications: - Buscopan Tablets should not be administered to patients with myasthenia gravis, megacolon and narrow angle glaucoma. In addition, they should not be given to patients with a known hypersensitivity to hyoscine-N-butylbromide or any other component of the product. Adverse Effects: CNS: dizziness, anaphylactic reactions, anaphylactic shock, increased ICP, disorientation, restlessness, irritability, dizziness, drowsiness, headache, confusion, hallucination, delirium, impaired memory CV: hypotension, tachycardia, palpitations, flushing GI: Dry mouth, constipation, nausea, epigastric distress DERM: flushing, dyshidrosis GU: Urinary retention, urinary hesitancy Resp: dyspnea, bronchial plugging, depressed respiration EENT: mydriasis, dilated pupils, blurred vision, photopobia, increased intraocular pressure, difficulty of swallowing. Nursing Considerations: - Drug compatibility should be monitored closely in patients requiring adjunctive therapy - Avoid driving & operating machinery after parenteral administration. - Avoid strict heat - Raise side rails as a precaution because some patients become temporarily excited or disoriented and some develop amnesia or become drowsy. - Reorient patient, as needed, Tolerance may develop when therapy is prolonged - Atropine-like toxicity may cause dose related adverse reactions. Individual tolerance varies greatly - Overdose may cause curare-like effects, such as respiratory paralysis. Keep emergency equipment available.