Classification: Cefditoren, As This Agent May Cause
Cefixime is an oral third-generation cephalosporin antibiotic prescribed for gonorrhea and other bacterial infections. It works by binding to the bacterial cell wall membrane and causing cell death. Common side effects include diarrhea and rash. The medication should be taken with food once daily for 5 days to treat gonorrhea, and as a single 400mg dose for other infections. Patients should finish the full course of medication and see a doctor if side effects occur.
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Classification: Cefditoren, As This Agent May Cause
Cefixime is an oral third-generation cephalosporin antibiotic prescribed for gonorrhea and other bacterial infections. It works by binding to the bacterial cell wall membrane and causing cell death. Common side effects include diarrhea and rash. The medication should be taken with food once daily for 5 days to treat gonorrhea, and as a single 400mg dose for other infections. Patients should finish the full course of medication and see a doctor if side effects occur.
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Prescribed Medication Prescribed Dosage, Frequency and Route of Administration:
Brand Name: Suprax 00 mg once daily; Gonorrhea—400
mg single dose. Generic Name: Cefixime Therapeutic Dosage: 400mg /tab OD x 5 days Drug Classification Mechanisms of Action (General Action) Patient Teaching Nursing Responsibilities Classification Bind to the bacterial cell wall membrane, Instruct patient to take medication around the Assess for infection (vital signs; appearance of Therapeutic: anti-infectives causing cell clock wound, sputum, urine, and stool; WBC) at Pharmacologic: third-generation death. Therapeutic Effects: Bactericidal and to finish the medication completely, even if beginning cephalosporins action feeling of and throughout therapy. against susceptible bacteria. Spectrum: better. Take missed doses as soon as possible ● Before initiating therapy, obtain a history to Similar to unless almost time for next dose; do not double determine that of second-generation cephalosporins, doses. Advise patient that sharing of this previous use of and reactions to penicillins or but activity medication cephalosporins. Persons with a negative history of against staphylococci is less, whereas may be dangerous. penicillin sensitivity may still have an allergic activity against ● Pedi: Instruct parents or caregivers to use response. gram-negative pathogens is greater, even calibrated ● Obtain specimens for culture and sensitivity for organisms measuring device with liquid preparations. before resistant to first- and second-generation ● Advise patient to report signs of superinfection initiating therapy. First dose may be given before agents (furry overgrowth on the tongue, vaginal itching receiving Laboratory Tests/Results Contraindications or results. Relevant to the Medication discharge, loose or foul-smelling stools) and ● Observe for signs and symptoms of anaphylaxis Lab Test Considerations: May allergy. (rash, pruritus, laryngeal edema, wheezing cause positive results Hypersensitivity to cephalosporins; ● Instruct patient to notify health care continue drug and notify health care professional for Coombs’ test in patients Serious hypersensitivity to penicillins; professional if immediately if these symptoms occur. Keep receiving high Pedi: rash, fever and diarrhea develop, especially if epinephrine, doses or in neonates whose mothers Premature neonates up to a postmenstrual stool an antihistamine, and resuscitation equipment were given age of 41 wk contains blood, pus, or mucus. Advise patient not close by in the event of an anaphylactic reaction. cephalosporins before delivery. (ceftriaxone only); Pedi: to ● Monitor bowel function. Diarrhea, abdominal ● Monitor prothrombin time and Hyperbilirubinemic neonates treat diarrhea without consulting health care cramping, fever, and bloody stools should be assess patient for (may lead to bilirubin encephalopathy); professional. reported bleeding (guaiac stools; check for Pedi: Neonates to health care professional promptly as a sign hematuria, bleeding _28 days requiring calcium-containing IV of Clostridium difficile-associated diarrhea gums, ecchymosis) daily in patients solutions (q (CDAD). receiving risk of precipitation formation); Carnitine May begin up to several wk following cessation of cefditoren, as this agent may cause deficiency or hypoprothrombinemia. inborn errors of metabolism (cefditoren therapy. ● May causeqserum AST, ALT, only); Hypersensitivity ● Assess patient for skin rash frequently during alkaline phosphatase, to milk protein (ceftidoren only; contains therapy. bilirubin, LDH, BUN, and serum sodium Discontinue at first sign of rash; may be creatinine. caseinate). lifethreatening. ● May rarely cause leukopenia, Stevens-Johnson syndrome may develop. neutropenia, agranulocytosis, Treat symptomatically; may recur once thrombocytopenia, eosinophilia, treatment is stopped. lymphocytosis, and thrombocytosis. Drug-Drug Interactions Food-Drug Interactions Drug-Drug: Probenecidpexcretion andqserum levels (cefdinir, cefditoren, cefixime, cefotaxime, cefpodoxime, ceftriaxone). Concurrent use of loop diuretics, aminoglycosides, or NSAIDs mayqrisk of nephrotoxicity. Antacidspabsorption of cefdinir, cefditoren, and cefpodoxime. Iron supplementspabsorption of cefdinir. H2-receptor antagonistspabsorption of cefditoren and cefpodoxime. Cefixime may qcarbamazepine levels. Ceftriaxone should not be administered concomitantly with any calcium-containing solutions. Ceftriaxone mayqrisk of bleeding with warfarin.
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