azithromycin package insert ceftin

Dosing (Adults): (Oral): 500mg to 1g po q12h or 250mg to 1gm q6h. CEFTIN is a semisynthetic, broad-spectrum cephalosporin antibiotic for oral administration. CEFTIN and other antibacterial drugs, CEFTIN should be used only to treat or prevent infections that are proven or strongly suspected to be caused by bacteria. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure.Hemolytic anemia, leukopenia, pancytopenia, thrombocytopenia.Hepatic impairment including hepatitis and cholestasis, jaundice.Angioedema, erythema multiforme, Stevens‑Johnson syndrome, toxic epidermal necrolysis, urticaria.Cefuroxime axetil may affect the gut flora, leading to lower estrogen reabsorption and reduced efficacy of combined oral estrogen/progesterone contraceptives.

0000002783 00000 n 0000010095 00000 n Thirteen (1.4%) U.S. pediatric subjects discontinued therapy due to the taste and/or problems with drug administration.The adverse reactions in Table 7 are for U.S. subjects (n = 931) treated with Ceftin in multiple‑dose clinical trials.The following adverse reactions occurred in less than 1% but greater than 0.1% of U.S. subjects (n = 931) treated with Ceftin for oral suspension in multiple‑dose clinical trials.The following adverse reactions have been identified during post-approval use of Ceftin.

0000005618 00000 n The discontinuations were primarily for gastrointestinal disturbances, usually diarrhea or vomiting. 0000006737 00000 n 0000000954 00000 n Ceftin is contraindicated in patients with a known hypersensitivity to Ceftin or other β-lactam antibacterial drugs If CDAD is suspected or confirmed, ongoing antibiotic use not directed against The possibility of superinfections with fungal or bacterial pathogens should be considered during therapy.Prescribing Ceftin either in the absence of a proven or strongly suspected bacterial infection or a prophylactic indication is unlikely to provide benefit to the patient and increases the risk of the development of drug‑resistant bacteria.Ceftin for oral suspension 125 mg/5 mL contains phenylalanine 11.8 mg per 5 mL (1 teaspoonful) of reconstituted suspension. In the absence of such data, local epidemiology and susceptibility patterns may contribute to the empiric selection of therapy.Administer Ceftin tablets as described in the dosage guidelines table below with or without food.Acute bacterial maxillary sinusitis (mild to moderate)Administer Ceftin for oral suspension as described in the dosage guidelines table below with food.Prepare a suspension at the time of dispensing as follows:A dosage interval adjustment is required for patients whose creatinine clearance is less than 30 mL/min, as listed in Table 4 below, because cefuroxime is eliminated primarily by the kidney [see Clinical Pharmacology (12.3)].A single additional standard dose should be given at the end of each dialysisCeftin tablets are white, capsule‑shaped, film‑coated tablets available in the following strengths:Ceftin for oral suspension is provided as dry, white to off‑white, tutti‑frutti–flavored powder. ZITHROMAX for oral suspension is supplied in bottles containing azithromycin dihydrate powder equivalent to 300 mg, 600 mg, 900 mg, or 1200 mg azithromycin per bottle and the following inactive ingredients: sucrose; sodium phosphate, tribasic, anhydrous; hydroxypropyl cellulose; xanthan gum; FD&C Red #40; and spray dried artificial cherry, creme de vanilla, and banana flavors.

They can also spread through oral sex and cause infections within the genital area. Reported clinical experience has not identified differences in responses between the elderly and younger adult patients, but greater sensitivity of some older individuals cannot be ruled out.Cefuroxime is substantially excreted by the kidney, and the risk of adverse reactions may be greater in patients with impaired renal function.

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