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-Gestational age 32 to 37 weeks: 50 mg/kg orally in divided doses every 12 hours . -Dispense in a tight container. . -At least 40 kg: 250 mg orally every 8 hours or 500 mg every 12 hours . Up to 1 week of age: . 
Immediate-release: . cough . Canadian labeling: Additional contraindications (not in US labeling): Infectious mononucleosis (suspected or confirmed) . Probenecid: May increase the serum concentration of Penicillins. Monitor therapy . -Immediate-release: 500 mg orally 3 times a day for 7 to 10 days . rash . May be taken with or without food. . IDSA recommendations: . Test Interactions . difficulty with swallowing . Store at room temperature away from moisture, heat, and light. . For Healthcare Professionals . 
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Mild to Moderate Infection: . IDSA and the Pediatric Infectious Diseases Society recommendations: . -Patients may require prophylaxis to complete an antimicrobial regimen of up to 60 days from onset of illness. . Suspension Reconstituted, Oral: .This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088. . -Bioterrorism-related cases: To complete an antimicrobial regimen of up to 60 days from onset of illness . Duration of Therapy: . -Gestational age 32 to 37 weeks: 50 mg/kg orally in divided doses every 12 hours .fever . Children в‰Ґ6 years and Adolescents: Oral: 250 mg every 12 hours; Note: The decision to discontinue penicillin prophylaxis after 5 years of age in children who have not experienced invasive pneumococcal infection and have received recommended pneumococcal immunizations is patient and clinician dependent. . Some side effects may not be reported. You may report them to the FDA. . Comments: .IDSA and the Pediatric Infectious Diseases Society recommendations: . Data not available . Get emergency medical help if you have signs of an allergic reaction to amoxicillin capsules dosage  (hives, difficult breathing, swelling in your face or throat) or a severe skin reaction (fever, sore throat, burning eyes, skin pain, red or purple skin rash with blistering and peeling). . -The full course of therapy should be completed. .-Recommended as an alternative oral regimen for postexposure prophylaxis and cutaneous anthrax without systemic involvement; recommended for penicillin-susceptible strains . Rhinosinusitis, acute bacterial: Immediate release: Treatment of infections due to beta-lactamase-negative Streptococcus spp. (alpha- and beta-hemolytic isolates only), S. pneumoniae, Staphylococcus spp., or H. influenzae. . Common (1% to 10%): Candidiasis, fungal/mycotic infection . Treatment of pulmonary exacerbations in patients without beta-lactamase-positive Haemophilus influenzae or Pseudomonas aeruginosa: Oral: 500 mg 3 times daily (Barker 2018; Finegold 1981) or 1 g 3 times daily (Prigogine 1988) for up to 14 days (Barker 2018; ERS <Polverino>2017]). . 
 
amoxicillin 1000 mg tablet  belongs to the group of medicines known as penicillins. . Inhalational, postexposure prophylaxis: Infants, Children, and Adolescents: Oral: 75 mg/kg/day in divided doses every 8 hours for 60 days after exposure; maximum dose: 1,000 mg/dose (AAP <Bradley>2014]). . Vitamin K Antagonists (eg, warfarin): Penicillins may enhance the anticoagulant effect of Vitamin K Antagonists. Monitor therapy . Dosage form specific issues: . 
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-Current guidelines should be consulted for additional information. . black, hairy tongue . Based on the IDSA guidelines for the management of prosthetic joint infection (PJI), amoxicillin adverse effects  is an effective and recommended agent for chronic oral antimicrobial suppression of PJI with beta-hemolytic streptococci, Enterococcus spp. (penicillin susceptible), and Cutibacterium spp. after completion of parenteral therapy. . Warnings/Precautions . 
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