Amoxicillin
Amoxicillin
FULL PRESCRIBING INFORMATION: CONTENTS*
- Rx only
- AMOXICILLIN DESCRIPTION
- CLINICAL PHARMACOLOGY
- AMOXICILLIN INDICATIONS AND USAGE
- AMOXICILLIN CONTRAINDICATIONS
- WARNINGS
- PRECAUTIONS
- AMOXICILLIN ADVERSE REACTIONS
- OVERDOSAGE
- AMOXICILLIN DOSAGE AND ADMINISTRATION
- HOW SUPPLIED
- CLINICAL STUDIES
- REFERENCES
- Manufacturer Information
FULL PRESCRIBING INFORMATION
Rx only
AMOXICILLIN DESCRIPTION
SRRRp
1619352
CLINICAL PHARMACOLOGY
Microbiology
in vitroINDICATIONS AND USAGE
Enterococcus faecalis
Staphylococcus
Streptococcus pneumoniae
Streptococcus
Escherichia coli
Haemophilus influenzae
Neisseria gonorrhoeae
Proteus mirabilis
Helicobacter pylori
Dilution Techniques
1ampicillinS. pneumoniaeS. pneumoniae
Enterococcus
MIC (mcg/mL) |
Interpretation |
≤8 |
Susceptible (S) |
≥16 |
Resistant (R) |
Staphylococcus a
MIC (mcg/mL) |
Interpretation |
≤0.25 |
Susceptible (S) |
≥0.5 |
Resistant (R) |
Streptococcus S. pneumoniae
MIC (mcg/mL) |
Interpretation |
≤0.25 |
Susceptible (S) |
0.5 to 4 |
Intermediate (I) |
≥8 |
Resistant (R) |
S. pneumoniaeb
Amoxicillin
MIC (mcg/mL) |
Interpretation |
≤2 |
Susceptible (S) |
4 |
Intermediate (I) |
≥8 |
Resistant (R) |
NOTE:
MIC (mcg/mL) |
Interpretation |
≤8 |
Susceptible (S) |
16 |
Intermediate (I) |
≥32 |
Resistant (R) |
H. influenzaec
MIC (mcg/mL) |
Interpretation |
≤1 |
Susceptible (S) |
2 |
Intermediate (I) |
≥4 |
Resistant (R) |
H. influenzae Haemophilus1
ampicillin
Microorganism |
MIC Range mcg/mL) |
E. coli ATCC 25922 |
2 to 8 |
E. faecalis ATCC 29212 |
0.5 to 2 |
H. influenzae ATCC 49247d |
2 to 8 |
S. aureus ATCC 29213 |
0.25 to 1 |
amoxicillin
Microorganism |
MIC Range (mcg/mL) |
S. pneumoniae ATCC 49619e |
0.03 to 0.12 |
H. influenzae1
S. pneumoniae
Diffusion Techniques
2S. pneumoniaeampicillin
Enterococcus
Zone Diameter (mm) |
Interpretation |
≥17 |
Susceptible (S) |
≤16 |
Resistant (R) |
Zone Diameter (mm) |
Interpretation |
≥29 |
Susceptible (S) |
≤28 |
Resistant (R) |
Zone Diameter (mm) |
Interpretation |
≥26 |
Susceptible (S) |
19 to 25 |
Intermediate (I) |
≤18 |
Resistant (R) |
NOTE:Spneumoniae
S. pneumoniae
S. pneumoniaeS. pneumoniae
Zone Diameter (mm) |
Interpretation |
≥17 |
Susceptible (S) |
14 to 16 |
Intermediate (I) |
≤13 |
Resistant (R) |
Zone Diameter (mm) |
Interpretation |
≥22 |
Susceptible (S) |
19 to 21 |
Intermediate (I) |
≤18 |
Resistant (R) |
H. influenzaeHaemophilus
2
ampicillin
Microorganism |
Zone Diameter (mm) |
E. coli ATCC 25922 |
16 to 22 |
H. influenzae ATCC 49247h |
13 to 21 |
S. aureus ATCC 25923 |
27 to 35 |
oxacillin
Microorganism |
Zone Diameter (mm) |
S. pneumoniae ATCC 49619i |
8 to 12 |
H. influenzae2
S. pneumoniae
2
Helicobacter pylori
In vitroH. pylori
AMOXICILLIN INDICATIONS AND USAGE
Infections of the ear, nose, and throatStreptococcusS. pneumoniaeStaphylococcusH. influenzae
Infections of the genitourinary tractE. coli, P. mirabilisE. faecalis
Infections of the skin and skin structureStreptococcusStaphylococcusE. coli
Infections of the lower respiratory tractStreptococcusS. pneumoniae, StaphylococcusH. influenzae
Gonorrhea, acute uncomplicated (ano-genital and urethral infections)N. gonorrhoeae
H. pylori eradication to reduce the risk of duodenal ulcer recurrence
Amoxicillin/clarithromycin/lansoprazole
H. pyloriH. pyloriH. pyloriCLINICAL STUDIESDOSAGE AND ADMINISTRATION
Amoxicillin/lansoprazole
H. pyloriwho are either allergic or intolerant to clarithromycin or in whom resistance to clarithromycin is known or suspected.H. pyloriCLINICAL STUDIESDOSAGE AND ADMINISTRATION
AMOXICILLIN CONTRAINDICATIONS
WARNINGS
SERIOUS ANAPHYLACTIC REACTIONS REQUIRE IMMEDIATE EMERGENCY TREATMENT WITH EPINEPHRINE. OXYGEN, INTRAVENOUS STEROIDS, AND AIRWAY MANAGEMENT, INCLUDING INTUBATION, SHOULD ALSO BE ADMINISTERED AS INDICATED.
Clostridium difficile C. difficile.
C. difficile C. difficile
C. difficileC. difficile
PRECAUTIONS
General
Information for Patients
Laboratory Tests
Drug Interactions
in vitro
Drug/Laboratory Test Interactions
®®
Carcinogenesis, Mutagenesis, Impairment of Fertility
2
Pregnancy
Teratogenic Effects
Labor and Delivery
Nursing Mothers
Pediatric Use
DOSAGE AND ADMINISTRATION: Neonates and Infants
Geriatric Use
AMOXICILLIN ADVERSE REACTIONS
Infections and Infestations
Gastrointestinal
WARNINGS
Hypersensitivity Reactions
WARNINGS
NOTE:
Liver
Renal
OVERDOSAGE
Hemic and Lymphatic Systems
Central Nervous System
Miscellaneous
Combination Therapy with Clarithromycin and Lansoprazole
Amoxicillin/Clarithromycin/Lansoprazole
Amoxicillin/Lansoprazole
OVERDOSAGE
3
AMOXICILLIN DOSAGE AND ADMINISTRATION
Neonates and Infants Aged ≤12 Weeks (≤3 Months)
Adults and Pediatric Patients >3 Months
* Dosing for infections caused by less susceptible organisms should follow the recommendations for severe infections. † The children’s dosage is intended for individuals whose weight is less than 40 kg. Children weighing 40 kg or more should be dosed according to the adult recommendations. |
|||
Infection |
Severity* |
Usual Adult Dose |
Usual Dose for Children >3 Months† |
Ear/Nose/Throat |
Mild/Moderate |
500 mg every 12 hours or 250 mg every 8 hours |
25 mg/kg/day in divided doses every 12 hours or 20 mg/kg/day in divided doses every 8 hours |
Severe |
875 mg every 12 hours or 500 mg every 8 hours |
45 mg/kg/day in divided doses every 12 hours or 40 mg/kg/day in divided doses every 8 hours |
|
Lower Respiratory Tract |
Mild/Moderate or Severe |
875 mg every 12 hours or 500 mg every 8 hours |
45 mg/kg/day in divided doses every 12 hours or 40 mg/kg/day in divided doses every 8 hours |
Skin/Skin Structure |
Mild/Moderate |
500 mg every 12 hours or 250 mg every 8 hours |
25 mg/kg/day in divided doses every 12 hours or 20 mg/kg/day in divided doses every 8 hours |
Severe |
875 mg every 12 hours or 500 mg every 8 hours |
45 mg/kg/day in divided doses every 12 hours or 40 mg/kg/day in divided doses every 8 hours |
|
Genitourinary Tract |
Mild/Moderate |
500 mg every 12 hours or 250 mg every 8 hours |
25 mg/kg/day in divided doses every 12 hours or 20 mg/kg/day in divided doses every 8 hours |
Severe |
875 mg every 12 hours or 500 mg every 8 hours |
45 mg/kg/day in divided doses every 12 hours or 40 mg/kg/day in divided doses every 8 hours |
|
Gonorrhea Acute, uncomplicated ano-genital and urethral infections in males and females |
|
3 grams as single oral dose |
Prepubertal children: 50 mg/kg amoxicillin, combined with 25 mg/kg probenecid as a single dose. NOTE: SINCE PROBENECID IS CONTRAINDICATED IN CHILDREN UNDER 2 YEARS, DO NOT USE THIS REGIMEN IN THESE CASES. |
PRECAUTIONS: Laboratory Tests
General
Streptococcus pyogenes
H. pylori Eradication to Reduce the Risk of Duodenal Ulcer Recurrence
Amoxicillin/clarithromycin/lansoprazole
INDICATIONS AND USAGE
Amoxicillin/lansoprazole
INDICATIONS AND USAGE
Dosing Recommendations for Adults with Impaired Renal Function
There are currently no dosing recommendations for pediatric patients with impaired renal function.
Directions for Mixing Oral Suspension
200 mg/5 mL
Amount of Water
Bottle SizeRequired for Reconstitution
400 mg/5 mL
Amount of Water
Bottle Size Required for Reconstitution
NOTE:
HOW SUPPLIED
Amoxicillin for Oral Suspension, USP: Each 5 mL of reconstituted bubble-gum-flavored pink suspension contains 200 or 400 mg amoxicillin as the trihydrate.
Amoxicillin is supplied as follows:
NDC | Strength | Quantity/Form |
55045-2992-2 | 400 mg/5 mL | 100 mL |
Store dry powder at 20° to 25°C (68° to 77°F); excursions permitted to 15° to 30°C (59° to 86°F) [see USP Controlled Room Temperature].
CLINICAL STUDIES
H. pylori Eradication to Reduce the Risk of Duodenal Ulcer Recurrence
H. pyloriH. pylori
H. pylori
H. pylori
H. pylori Eradication Rates – Triple Therapy (amoxicillin/clarithromycin/lansoprazole)
Percent of Patients Cured [95% Confidence Interval] (Number of Patients)
* This analysis was based on evaluable patients with confirmed duodenal ulcer (active or within 1 year) and H. pylori infection at baseline defined as at least 2 of 3 positive endoscopic tests from CLOtest®, (Delta West Ltd., Bentley, Australia), histology, and/or culture. Patients were included in the analysis if they completed the study. Additionally, if patients dropped out of the study due to an adverse event related to the study drug, they were included in the analysis as failures of therapy. † Patients were included in the analysis if they had documented H. pylori infection at baseline as defined above and had a confirmed duodenal ulcer (active or within 1 year). All dropouts were included as failures of therapy. ‡ (p<0.05) versus lansoprazole/amoxicillin and lansoprazole/clarithromycin dual therapy. § (p<0.05) versus clarithromycin/amoxicillin dual therapy. |
||
Study |
Triple Therapy |
Triple Therapy |
Evaluable Analysis* |
Intent-to-Treat Analysis† |
|
Study 1 |
92‡ [80 - 97.7] (n = 48) |
86‡ [73.3 - 93.5] (n = 55) |
Study 2 |
86§ [75.7 - 93.6] (n = 66) |
83§ [72 - 90.8] (n = 70) |
H. pylori Eradication Rates – Dual Therapy (amoxicillin/lansoprazole)
Percent of Patients Cured [95% Confidence Interval] (Number of Patients)
* This analysis was based on evaluable patients with confirmed duodenal ulcer (active or within 1 year) and H. pylori infection at baseline defined as at least 2 of 3 positive endoscopic tests from CLOtest®, histology, and/or culture. Patients were included in the analysis if they completed the study. Additionally, if patients dropped out of the study due to an adverse event related to the study drug, they were included in the analysis as failures of therapy. † Patients were included in the analysis if they had documented H. pylori infection at baseline as defined above and had a confirmed duodenal ulcer (active or within 1 year). All dropouts were included as failures of therapy. ‡ (p<0.05) versus lansoprazole alone. § (p<0.05) versus lansoprazole alone or amoxicillin alone. |
||
Study |
Dual Therapy |
Dual Therapy |
Evaluable Analysis* |
Intent-to-Treat Analysis† |
|
Study 1 |
77‡ [62.5 - 87.2] (n = 51) |
70‡ [56.8 - 81.2] (n = 60) |
Study 2 |
66§ [51.9 - 77.5] (n = 58) |
61§ [48.5 - 72.9] (n = 67) |
REFERENCES
- National Committee for Clinical Laboratory Standards. Methods for Dilution Antimicrobial Susceptibility Tests for Bacteria that Grow Aerobically – Fourth Edition; Approved Standard NCCLS Document M7-A4, Vol. 17, No. 2. NCCLS, Wayne, PA, January 1997.
- National Committee for Clinical Laboratory Standards. Performance Standards for Antimicrobial Disk Susceptibility Tests – Sixth Edition; Approved Standard NCCLS Document M2-A6, Vol. 17, No. 1. NCCLS, Wayne, PA, January 1997.
- Swanson-Biearman B, Dean BS, Lopez G, Krenzelok EP. The effects of penicillin and cephalosporin ingestions in children less than six years of age. Vet Hum Toxicol. 1988;30:66-67.
CLINITEST is a registered trademark of Miles, Inc.
CLINISTIX is a registered trademark of Bayer Corporation.
CLOtest is a registered trademark of Kimberly-Clark Corporation.
Manufacturer Information
Manufactured By:
Aurobindo Pharma Limited
Hyderabad-500 072, India
Manufactured for:
Aurobindo Pharma USA, Inc.
2400 Route 130 North
Dayton, NJ 08810
As NDC:
65862-0071-01 For 55045-2992-2 Amoxicillin 400 mg
Repackaged By:
Dispensing Solutions Inc.
3000 West Warner Ave
Santa Ana, CA 92704
United States
AmoxicillinAmoxicillin POWDER, FOR SUSPENSION
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