Classes
DEA Class; Rx
Common Brand Names; Amoxil, Moxatag (DSC), Trimox
- Penicillins, Amino
Description
Oral semisynthetic aminopenicillin similar to ampicillin; not stable to beta-lactamases of either gram-positive or gram-negative bacteria
Used commonly for otitis media, pneumonia, sinusitis, and skin infections
Higher doses necessary for respiratory infections due to S. pneumoniae resistance
Indications
Indicated for the treatment of Ear, Nose, & Throat Infections
Indicated for the treatment of Genitourinary Tract Infections
Indicated for the treatment of Skin & Skin Structure Infections
Indicated for the treatment of Lower Respiratory Tract Infections
Indicated for the treatment of Helicobacter Pylori
Indicated for the treatment of Anthrax
Indicated for the treatment of Infective Endocarditis
Indicated for the treatment of Lyme Disease (Off-label), Chlamydial Infection in Pregnant Women (Off-label)
Contraindications
Documented hypersensitivity to penicillins, cephalosporins, imipenem
Adverse Effects
- Anaphylaxis
- Anemia
- AST/ALT elevation
- Mucocutaneous candidiasis
- Diarrhea
- Headache
- Nausea
- Vomiting
- Rash
- Pseudomembranous colitis
- Serum sickness-like reactions
- Mucocutaneous candidiasis
- Gastrointestinal (eg, black hairy tongue and hemorrhagic/pseudomembranous colitis, which may occur during or after treatment)
Warnings
Anaphylaxis has been reported rarely but is more likely to occur following parenteral therapy with penicillins
Clostridium difficile-associated diarrhea (CDAD) has been reported with use of nearly all antibacterial agents; severity may range from mild diarrhea to fatal colitis; CDAD may occur over 2 months after discontinuation of therapy; if CDAD is suspected or confirmed, discontinue immediately and begin appropriate fluid and electrolyte management, protein supplementation, antibiotic treatment of C difficile, and surgical evaluation
Do not administer in patients with infectious mononucleosis because of risk of development of erythematous skin rash
Do not administer to patients in the absence of a proven or suspected bacterial infection because of risk of development of drug-resistant bacteria
Superinfections with bacterial or fungal pathogens may occur during therapy; if suspected, discontinue immediately and begin appropriate treatment
Chewable tablets contain aspartame, which contains phenylalanine
Use caution in patients with allergy to cephalosporins, carbapenems
Endocarditis prophylaxis: use for only high-risk patients, as per recent AHA guidelines
High doses may cause false urine glucose test by some methods
May cause severe cutaneous adverse reactions (SCAR), such as Stevens-Johnson syndrome (SJS), toxic epidermal necrolysis (TEN), drug reaction with eosinophilia and systemic symptoms (DRESS), and acute generalized exanthematous pustulosis (AGEP); if patients develop a skin rash they should be monitored closely and therapy discontinued if lesions progress
Pregnancy and Lactation
Available data from published epidemiologic studies and pharmacovigilance case reports over several decades with amoxicillin use have not established drug-associated risks of major birth defects, miscarriage, or adverse maternal or fetal outcomes
Data from a published clinical lactation study reports that amoxicillin is present in human milk; published adverse effects with amoxicillin exposure in breastfed infant include diarrhea
Maximum Dosage
1,750 mg/day PO is FDA-approved maximum; however, doses up to 3 g/day PO have been used off-label.
1,750 mg/day PO is FDA-approved maximum; however, doses up to 3 g/day PO have been used off-label.
45 mg/kg/day (Max: 1,750 mg/day) PO is FDA-approved maximum; however, doses up to 100 mg/kg/day (Max: 4 g/day) PO have been used off-label.
45 mg/kg/day (Max: 1,750 mg/day) PO is FDA-approved maximum; however, doses up to 100 mg/kg/day (Max: 4 g/day) PO have been used off-label.
4 to 11 months: 45 mg/kg/day PO is FDA-approved maximum; however, doses up to 100 mg/kg/day PO have been used off-label.
1 to 3 months: 30 mg/kg/day PO is FDA-approved maximum; however, doses up to 100 mg/kg/day PO have been used off-label.
30 mg/kg/day PO is FDA-approved maximum; however, doses up to 75 mg/kg/day PO have been used off-label.
How supplied
Amoxicillin
oral solution
- 125mg/5mL
- 200mg/5mL
- 250mg/5mL
- 400mg/5mL
capsule
- 250mg
- 500mg
tablet
- 500mg
- 875mg
tablet, chewable
- 125mg
- 250mg