Augmentin Powder For Oral Suspension 125-31.25Mg Drug Medication Dosage Information
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Augmentin: Powder for oral suspension (125-31.25mg)

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Augmentin 125mg/5ml for Susp
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Augmentin 125mg/5ml for Susp
Drug Image file default-drug-image.png
Augmentin 125mg/5ml for Susp
Drug Image file default-drug-image.png
Augmentin 125mg/5ml for Susp
Drug Image file default-drug-image.png
Augmentin 125mg/5ml for Susp

What is this Medicine?

AMOXICILLIN; CLAVULANIC ACID (a mox i SILL in; KLAV yoo lan ic AS id) is a penicillin antibiotic. It is used to treat certain kinds of bacterial infections. It will not work for colds, flu, or other viral infections.

CVS Pharmacy Patient Statistics for Augmentin: Powder for oral suspension(125-31.25mg)
Generic vs. Brand Name Usage*
*Brand contains same active ingredient but may not represent FDA-approved generic equivalent
Usage By Strength
In-Depth Information
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Augmentin 125mg/5ml Powder for Suspension

NDC: 435980012
  • Prescription Required
  • Not a Controlled Drug
    (CSA Schedule)
  • FDA Approved




FDA approved for the following conditions:
Impetigo, Cystitis, Skin And Skin Structure Infections, Urinary Tract Infection (UTI), Otitis Media

Sometimes used for but not FDA approved for the following conditions:
Pneumonia, Febrile Neutropenia, Pericoronitis, Dental Infection, Dentoalveolar Infection, Sinusitis, Periodontitis, Lower Respiratory Tract Infections, Actinomycotic Mycetoma, Melioidosis, Community-acquired Pneumonia

Storage Information
Store in original container
Discard any unused reconstituted product after 10 days
Store unreconstituted product at or below 77 degrees F
Store reconstituted product in refrigerator (36 to 46 degrees F)
Augmentin 125mg/5ml Powder for Suspension

Reported Side Effects for Augmentin 125mg/5ml Powder for Suspension

High Platelet Count Incidence:
<1.0%*
Severity: MODERATE
Onset: DELAYED
Yeast Infection Incidence:
1.0-6.0%*
Severity: MODERATE
Onset: DELAYED
Skin Rash Incidence:
1.0-3.0%*
Severity: MILD
Onset: EARLY
Vomiting Incidence:
1.0-8.0%*
Severity: MILD
Onset: EARLY
Vaginal Infection Incidence:
1.0%*
Severity: MODERATE
Onset: DELAYED
Upset Stomach Incidence:
2.1-3.0%*
Severity: MILD
Onset: EARLY
Hives Incidence:
3.0%*
Severity: MILD
Onset: RAPID
Loose Stools Incidence:
4.0-34.3%*
Severity: MILD
Onset: EARLY
Diaper Rash Incidence:
5.0-6.0%*
Severity: MILD
Onset: DELAYED
*This is an approximate aggregated range of reported side effects from clinical studies performed on this drug. Your experience with this drug may be different.
Pregnancy & Lactation Information
FIRST Trimester

Class B - Animal studies have revealed no evidence of harm to the fetus, however, there are no adequate and well-controlled studies in pregnant women. OR Animal studies have shown an adverse effect, but adequate and well-controlled studies in pregnant women have failed to demonstrate a risk to the fetus in any trimester.

SECOND Trimester

Class B - Animal studies have revealed no evidence of harm to the fetus, however, there are no adequate and well-controlled studies in pregnant women. OR Animal studies have shown an adverse effect, but adequate and well-controlled studies in pregnant women have failed to demonstrate a risk to the fetus in any trimester.

THIRD Trimester

Class B - Animal studies have revealed no evidence of harm to the fetus, however, there are no adequate and well-controlled studies in pregnant women. OR Animal studies have shown an adverse effect, but adequate and well-controlled studies in pregnant women have failed to demonstrate a risk to the fetus in any trimester.

Lactation

Compatible - This drug is generally safe to take by nursing mothers.


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