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Omnicef (generic name: cefdinir; brand names include: Sefdin / Adcef) is a semi-synthetic broad-spectrum antibiotic that belongs to a group of medicines known as third generation cephalosporin antibiotics.

Omnicef is one of the highest-selling cephalosporin antibiotics in the United States.

Omnicef is used for the treatment of various bacterial infections including pneumonia, bronchitis, otitis media, sinusitis, pharyngitis/tonsillitis, and skin and skin structure infections.





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Genitourinary side effects have included vaginal moniliasis (4% of women), vaginitis (1% of women), leukorrhea (0.2% of women), increased urine leukocytes (2%), increased urine protein (1%), increased microhematuria (1%), increased urine glucose (0.9%), increased urine specific gravity (0.6%), decreased urine specific gravity (0.2%), increased urine pH (0.2%). Cephalosporins as a class have been associated with false-positive tests for urine glucose. Acute Maxillary Sinusitis 300 mg q12h or 10 days diaper rash in an infant taking liquid cefdinir; Ocular adverse effects reported during postmarketing experience with cefdinir (the active ingredient contained in Omnicef) regardless of causality, have included conjunctivitis. Acute Bacterial Otitis Media caused by Haemophilus influenzae (including β-lactamase producing strains), Streptococcus pneumoniae (penicillin-susceptible strains only), and Moraxella catarrhalis (including β-lactamase producing strains). HOW SUPPLIED Before using this medication, tell your doctor or pharmacist your medical history, especially of: kidney disease, intestinal disease (colitis). Important information about Omnicef http://edmedics.net/frblg/achat-clomid/#prise-clomid-etant-enceinte
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Antibiotic medicines can cause diarrhea, which may be a sign of a new infection. If you have diarrhea that is watery or bloody, stop taking Omnicef and call your doctor. Do not use anti-diarrhea medicine unless your doctor tells you to. pale or yellowed skin, dark colored urine, fever, confusion or weakness; Applies to cefdinir: oral capsule, oral powder for reconstitution caused by Haemophilus influenzae (including β-lactamase producing strains), Haemophilus parainfluenzae (including β-lactamase producing strains), Streptococcus pneumoniae (penicillin-susceptible strains only), and Moraxella catarrhalis (including β lactamase producing strains). Community-Acquired Pneumonia 300 mg q12h 10 days
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Directions for Mixing Omnicef (cefdinir) for Oral Suspension Final Concentration Final Volume (mL) Amount of Water Directions Uncomplicated Skin and Skin Structure Infections 300 mg q12h 10 days The recommended dosage and duration of treatment for infections in pediatric patients are described in the following chart; the total daily dose for all infections is 14 mg/kg, up to a maximum dose of 600 mg per day. Once-daily dosing for 10 days is as effective as BID dosing. Once-daily dosing has not been studied in skin infections; therefore, OMNICEF (cefdinir) for Oral Suspension should be administered twice daily in this infection. OMNICEF (cefdinir) for Oral Suspension may be administered without regard to meals. fever, chills, body aches, flu symptoms; To reduce the development of drug-resistant bacteria and maintain the effectiveness of OMNICEF (cefdinir) and other antibacterial drugs, OMNICEF (cefdinir) should be used only to treat or prevent infections that are proven or strongly suspected to be caused by susceptible bacteria. When culture and susceptibility information are available, they should be considered in selecting or modifying antibacterial therapy. In the absence of such data, local epidemiology and susceptibility patterns may contribute to the empiric selection of therapy. pale or yellowed skin, dark colored urine, fever, confusion or weakness; where creatinine clearance is in mL/min, age is in years, weight is in kilograms, and serum creatinine is in mg/dL.(3)
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125 mg/5 mL Metabolic side effects have included increased gamma-glutamyltransferase (1%), increased alanine aminotransferase (0.7%), decreased bicarbonate (0.6%), increased phosphorus (0.6%), decreased phosphorus (0.3%), increased aspartate aminotransferase (0.4%), increased alkaline phosphatase (0.3%), increased blood urea nitrogen (0.3%), increased bilirubin (0.2%), increased lactate dehydrogenase (0.2%), and increased potassium (0.2%). Other

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125 mg/5 mL a history of intestinal problems, such as colitis; or headache, dizziness; OMNI-PAC™ carton of 3 unit-of-use, 5-day, seizure (convulsions); pale or yellowed skin, dark colored urine, fever, confusion or weakness; unusual bleeding;