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DRUG MECHANISM OF INDICATIONS CONTRAINDICATIO SIDE EFFECTS NURSING

ACTION N CONSIDERATIONS
IPRATROPIUM/ALBUTE Albuterol: Beta2- This product is used Hypersensitivity to Headache,  Monitor rate, depth,
ROL adrenergic to treat and prevent albuterol, ipratropium, dizziness, nausea, rhythm, type of
bronchodilator symptoms atropine and derivatives, dry mouth, shaking respiration; quality and
Brand name: Ipratropium (wheezing and soy, or peanut (tremors), rate of pulse.
Salbutamol  Assess lung sounds for
Ipratropium: shortness of breath) nervousness, or
wheezing
Classification:
Anticholinergic caused by cold symptoms (bronchoconstriction) and
Clinical: Bronchodilators (parasympatholytic) ongoing lung such as stuffy nose, rales.
agent; inhibits vagally disease (chronic sneezing, cough, or  Protect solution for
Dosage: mediated reflexes by obstructive sore throat. inhalation from light.
Nebulizer solution (generic) antagonizing pulmonary Store unused vials in foil
(2.5mg/0.5mg)/3mL acetylcholine action; disease-COPD whi pouch.
prevents increase in ch includes  Use nebulizer mouthpiece
Onset: intracellular calcium bronchitis and instead of face mask to
5-15 minutes concentration caused by emphysema). avoid blurred vision or
interaction of aggravation of narrow-
Administration: angle glaucoma.
acetylcholine with
Nebulizer solution  Can mix albuterol in
Administer via jet nebulizer muscarinic receptors on nebulizer for up to 1 hr.
connected to air compressor bronchial smooth  Ensure adequate
with adequate air flow muscle hydration, control
Equip with mouthpiece or environmental
suitable air mask temperature to prevent
hyperpyrexia.
 Have patient void before
taking medication to
avoid urinary retention.
 Teach patient proper use
of inhaler.

DRUG MECHANISM OF INDICATIONS CONTRAINDICATIO SIDE EFFECTS NURSING


ACTION N CONSIDERATIONS
Generic name: Mucolytic splits Inhalation: Adjunctive None known. IV: (10%): BASELINE ASSESSMENT
ACETYLCYSTEINE linkage of treatment for Nausea, vomiting. Mucolytic: Assess pretreatment
respirations for rate, depth,
mucoproteins, abnormally viscid (7%– 6%): Acute rhythm. IV antidote: Obtain
(Acetadote, Mucomyst, reducing viscosity of mucous secretions flushing, erythema. baseline labs and drug screen.
Parvolex, Fluimucil) pulmonary secretions. present in acute and (4%): Pruritus. For use as antidote, obtain
Acetaminophen chronic acetaminophen level to
determine need for treatment
Classification: toxicity: bronchopulmonary Frequent: with acetylcysteine.
PHARMACOTHERAPEUT Hepatoprotective by disease and pulmonary Inhalation:
IC: Respiratory inhalant, restoring heptic complications of cystic Stickiness on face, INTERVENTION/EVALUAT
intratracheal. glutathione and fibrosis and surgery, transient ION If bronchospasm occurs,
discontinue treatment, notify
CLINICAL: Mucolytic, enhancing nontoxic diagnostic bronchial unpleasant odor. physician; bronchodilator may
antidote. conjugation of studies. be added to therapy. Monitor
acetaminophen. Occasional: rate, depth, rhythm, type of
Dosage: Inhalation: respiration (abdominal,
Inhalation, Nebulization Therapeutic Effect: Increased bronchial thoracic). Observe sputum for
color, consistency, amount. IV
ADULTS, ELDERLY, Facilitates removal of secretions, throat antidote: Administer within 8 hrs
CHILDREN: 3–5 ml (20% pulmonary secretions irritation, nausea, of acetaminophen ingestion for
solution) 3–4 times a day or by coughing, postural vomiting, and maximal hepatic protection;
6–10 ml (10% solution) 3–4 drainage, mechanical rhinorrhea. Rare: ideally, within 4 hrs after
immediate-release and 2 hrs
times a day. Range: 1–10 ml means. Protects Inhalation: Rash. after liquid acetaminophen
(20% solution) q2–6h or 2–20 against PO: Facial edema, formulations.
ml (10% solution) q2–6h. acetaminophen bronchospasm,
overdose-induced wheezing, nausea, PATIENT/FAMILY
Administration: hepatotoxicity vomiting TEACHING •  Slight,
disagreeable sulfuric odor from
IV solution may be noticed during
initial administration but
Onset: Not indicated disappears quickly.  • 
Adequate hydration is important
part of therapy.  • Follow
guidelines for proper coughing
and deep breathing techniques.

DRUG MECHANISM INDICATIONS CONTRAINDICATIO SIDE EFFECTS NURSING


OF ACTION N CONSIDERATIONS
Generic name: Piperacillin: Treatment of Hypersensitivity to any Frequent: BASELINE ASSESSMENT
PIPERACILLIN SODIUM / Inhibits cell wall moderate to severe penicillin. Diarrhea, Question for history of allergies,
TAZOBACTAM SODIUM synthesis by bacterial headache, esp. to penicillins,
binding to infections, constipation, cephalosporins.
(Tazocin , Zosyn) bacterial cell including nausea, insomnia,
membranes. community- rash. INTERVENTION/EVALUAT
Classification: acquired/ ION Monitor daily pattern of
PHARMACOTHERAPEUT Therapeutic nosocomial Occasional: bowel activity, stool
IC: Penicillin Effect: pneumonia, intra- Vomiting, consistency; mild GI effects may
CLINICAL: Antibiotic Bactericidal. abdominal, pelvic, dyspepsia, be tolerable, but increasing
Tazobactam: skin, and skin pruritus, fever, severity may indicate onset of
Dosage: Inactivates structure agitation, antibiotic-associated colitis.
Severe Infections IV: bacterial beta- infections. candidiasis, Be alert for superinfection:
ADULTS, ELDERLY, and lactamase. Tazobactam dizziness, fever, vomiting, diarrhea, and
CHILDREN 12 YRS AND expands abdominal pain, anal/genital pruritus, oral
OLDER: 4.5 g q6–8h or Therapeutic piperacillin edema, anxiety, mucosal changes (ulceration,
3.375 g q6h. Maximum: 18 g Effect: Protects activity to include dyspnea, rhinitis. pain, and erythema).
daily. piperacillin from beta-lactamase- Monitor I&O, urinalysis.
enzymatic producing strains Monitor serum electrolytes, esp.
Administration: degradation, of S. aureus, H. potassium, and renal function
IV Reconstitution  extends its influenzae, tests.
•  Reconstitute each 1 g with spectrum of Bacteroides.
5 ml D5W or 0.9% NaCl. activity, prevents
Shake vigorously to bacterial
dissolve.  overgrowth.
•  Further dilute with at least
50 ml D5W or 0.9% NaCl.

Onset: Immediate

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