Medical term:
Omnicef
cefdinir
Pharmacologic class: Third-generation cephalosporin
Therapeutic class: Anti-infective
Pregnancy risk category B
Action
Interferes with bacterial cell-wall synthesis and division by binding to cell wall, causing cell to die. Active against gram-negative and gram-positive bacteria, with expanded activity against gram-negative bacteria. Exhibits minimal immunosuppressant activity.
Availability
Capsules: 300 mg
Oral suspension: 125 mg/5 ml in 60-and 100-ml bottles
Indications and dosages
➣ Acute bacterial otitis media caused by Haemophilus influenzae, Streptococcus pneumoniae, and Moraxella catarrhalis
Adults and children ages 13 and older: 300 mg P.O. q 12 hours or 600 mg P.O. q 24 hours for 10 days
Children ages 6 months to 12 years: 7 mg/kg P.O. q 12 hours for 5 to 10 days or 14 mg/kg P.O. q 24 hours for 10 days
➣ Uncomplicated skin and soft-tissue infections caused by Staphylococcus aureus and Streptococcus pyogenes
Adults and children ages 13 and older: 300 mg P.O. q 12 hours for 10 days. Maximum dosage is 600 mg/day.
➣ Acute maxillary sinusitis caused by H. influenzae, S. pneumoniae, and M. catarrhalis
Adults and children ages 13 and older: 300 mg P.O. q 12 hours or 600 mg P.O. q 24 hours for 10 days. Maximum dosage is 600 mg/day.
Children ages 6 months to 12 years: 7 mg/kg P.O. q 12 hours or 14 mg/kg P.O. q 24 hours for 10 days
➣ Pharyngitis or tonsillitis caused by S. pyogenes, chronic bronchitis caused by H. influenzae, S. pneumoniae, and M. catarrhalis
Adults and children ages 13 and older: 300 mg P.O. q 12 hours for 5 to 10 days or 600 mg P.O. q 24 hours for 10 days. Maximum dosage is 600 mg/day.
➣ Community-acquired pneumonia caused by H. influenzae, Haemophilus parainfluenzae, S. pneumoniae, and M. catarrhalis
Adults and children ages 13 and older: 300 mg P.O. q 12 hours for 10 days. Maximum dosage is 600 mg/day.
Dosage adjustment
• Renal impairment
Contraindications
• Hypersensitivity to cephalosporins or penicillins
Precautions
Use cautiously in:
• renal impairment, phenylketonuria
• history of GI disease (especially colitis)
• elderly patients
• pregnant or breastfeeding patients
• children.
Administration
• Obtain specimens for culture and sensitivity tests as necessary before starting therapy.
• Give with or without food.
• Administer 2 hours before or after iron supplements or antacids containing aluminum or magnesium.
• Give capsules, if possible, to diabetic patients (oral suspension contains 2.86 g of sucrose per teaspoon).
Adverse reactions
CNS: headache, lethargy, paresthesia, syncope, seizures
CV: hypotension, palpitations, chest pain, vasodilation
EENT: hearing loss
GI: nausea, vomiting, diarrhea, abdominal cramps, oral candidiasis,
pseudomembranous colitis
GU: vaginal candidiasis, nephrotoxicity
Hematologic: lymphocytosis, eosinophilia, bleeding tendency, hemolytic anemia, hypoprothrombinemia, neutropenia, thrombocytopenia, agranulocytosis, bone marrow depression
Hepatic: hepatomegaly, hepatic failure
Musculoskeletal: arthralgia
Respiratory: dyspnea
Skin: chills, fever, urticaria, maculopapular or erythematous rash
Other: superinfection, anaphylaxis, serum sickness
Interactions
Drug-drug. Aminoglycosides, loop diuretics: increased risk of nephrotoxicity
Antacids, iron-containing preparations: decreased cefdinir absorption
Probenecid: decreased excretion and increased blood level of cefdinir
Drug-diagnostic tests. Alanine aminotransferase, alkaline phosphatase, aspartate aminotransferase, bilirubin, blood urea nitrogen, creatinine, eosinophils, gamma-glutamyltransferase, lactate dehydrogenase: increased levels
Coombs' test, urinary 17-ketosteroids, nonenzyme-based urine glucose tests (such as Clinitest): false-positive results
Hemoglobin, platelets, white blood cells: decreased values
Drug-herbs. Angelica, anise, arnica, asafetida, bogbean, boldo, celery, chamomile, clove, danshen, fenugreek, feverfew, garlic, ginger, ginkgo, horse chestnut, horseradish, licorice, meadowsweet, onion, ginseng, papain, passionflower, poplar, prickly ash, quassia, red clover, turmeric, wild carrot, wild lettuce, willow: increased risk of bleeding
Patient monitoring
• Monitor CBC and kidney and liver function test results.
• Monitor for signs and symptoms of superinfection and other serious adverse reactions.
Patient teaching
• Tell patient he may take drug with or without food.
• Instruct patient to report persistent diarrhea (more than four episodes daily) and other adverse effects.
• If patient uses antacids or iron-containing preparations (such as iron supplements), tell him to take these 2 hours before or after cefdinir.
• Inform patient that drug may temporarily discolor stools.
• As appropriate, review all other significant and life-threatening adverse reactions and interactions, especially those related to the drugs, tests, and herbs mentioned above.
cefdinir
(sef-di-nir) ,Omnicef
(trade name)Classification
Therapeutic: anti infectivesPharmacologic: third generation cephalosporins
Indications
- Community-acquired pneumonia (adults only),
- Acute exacerbations of chronic bronchitis (adults only),
- Acute maxillary sinusitis,
- Pharyngitis and tonsillitis,
- Uncomplicated skin and skin structure infections,
- Acute bacterial otitis media (children only).
Action
Therapeutic effects
- Staphylococcus aureus,
- Streptococcus pneumoniae,
- Streptococcus pyogenes.
- Haemophilus influenzae(including β-lactamase-producing strains),
- Haemophilus parainfluenzae(including β-lactamase-producing strains),
- Moraxella catarrhalis (including β-lactamase-producing strains).
Pharmacokinetics
Time/action profile (blood levels)
ROUTE | ONSET | PEAK | DURATION |
PO | rapid | 2–4 hr | 12–24 hr |
Contraindications/Precautions
Adverse Reactions/Side Effects
Central nervous system
- seizures (life-threatening)
- headache
Gastrointestinal
- pseudomembranous colitis (life-threatening)
- diarrhea (most frequent)
- vomiting (most frequent)
- abdominal pain
- nausea
Genitourinary
- vaginal moniliasis
- vaginitis
Dermatologic
- rash (most frequent)
- pruritus
Miscellaneous
- allergic reactions including anaphylaxis (life-threatening)
Interactions
Drug-Drug interaction
Antacids and iron supplements ↓ absorption (administer at least 2 hr before or 2 hr after).Probenecid ↓ excretion and ↑ blood levels.Route/Dosage
Renal Impairment
(Adults and Children ≥13 yr) CCr <30 mL/min—300 mg every 24 hr.Renal Impairment
(Children 6 mo-12 yr) CCr <30 mL/min—7 mg/kg every 24 hr.Availability (generic available)
Nursing implications
Nursing assessment
- Assess patient for infection (vital signs; appearance of wound, sputum, urine, and stool; WBC) at beginning of and throughout therapy.
- Before initiating therapy, obtain a history to determine previous use of and reactions to penicillins or cephalosporins. Persons with a negative history of penicillin sensitivity may still have an allergic response.
- Obtain specimens for culture and sensitivity before initiating therapy. First dose may be given before receiving results.
- Observe patient for signs and symptoms of anaphylaxis (rash, pruritus, laryngeal edema, wheezing). Discontinue drug and notify physician or other health care professional immediately if these symptoms occur. Keep epinephrine, an antihistamine, and resuscitation equipment close by in case of an anaphylactic reaction.
- Monitor bowel function. Diarrhea, abdominal cramping, fever, and bloody stools should be reported to health care professional promptly as a sign of pseudomembranous colitis. May begin up to several weeks following cessation of therapy.
- Lab Test Considerations: May cause positive results for Coombs’ test.
- May cause increased serum AST, ALT, alkaline phosphatase, bilirubin, LDH, and BUN.
- May rarely cause leukopenia, eosinophilia, lymphocytosis, and thrombocytosis.
Potential Nursing Diagnoses
Risk for infection (Indications, Side Effects)Diarrhea (Adverse Reactions)
Deficient knowledge, related to medication regimen (Patient/Family Teaching)
Implementation
- Oral: Administer around the clock. May be administered without regard to food. Shake oral suspension well before administering. Suspension can be stored at room temperature for up to 10 days.
- Do not administer within 2 hr before or after antacids or iron supplements.
Patient/Family Teaching
- Instruct patient to take medication around the clock at evenly spaced times and to finish the medication completely as directed, even if feeling better. Take missed doses as soon as possible unless almost time for next dose; do not double doses. Instruct patient to use calibrated measuring device with suspension. Advise patient that sharing this medication may be dangerous.
- Advise patient to report signs of superinfection (furry overgrowth on the tongue, vaginal itching or discharge, loose or foul-smelling stools) and allergy.
- Instruct patient to notify health care professional if fever and diarrhea develop, especially if diarrhea contains blood, mucus, or pus. Advise patient not to treat diarrhea without consulting health care professional.
Evaluation/Desired Outcomes
- Resolution of signs and symptoms of infection. Length of time for complete resolution depends on the organism and site of infection.
Omnicef
(ōm′nĭ-sĕf′)Omnicef®
Cefdinir Infectious disease A cephalosporin used for community-acquired pneumonia, exacerbation of chronic bronchitis, bacterial sinusitis, pharyngitis and tonsillitis related to strep throat, uncomplicated skin infections; in children, for acute bacterial otitis media. See Cephalosporin.Latest Searches:
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