Amoxicillin, Clavulanate Potassium Powder For Oral Suspension 200-28.5Mg Drug Medication Dosage Information
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Amoxicillin, Clavulanate Potassium: Powder for oral suspension (200-28.5mg)

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Amox/Clav 200-28.5mg/5ml Pwd
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Amox/Clav 200-28.5mg/5ml Pwd
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Amox/Clav 200-28.5mg/5mL Pwd
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Amox/Clav 200-28.5mg/5ml Pwd
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Amox/Clav 200mg/5ml Pwd

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 Amoxicillin, Clavulanate Potassium: Powder for oral suspension(200-28.5mg)
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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Amoxicillin/Clavulanate Potassium 200mg-28.5mg/5ml Powder for Suspension

NDC: 666851011
  • 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 between 59 to 77 degrees F
Amoxicillin/Clavulanate Potassium 200mg-28.5mg/5ml Powder for Suspension

Reported Side Effects for Amoxicillin/Clavulanate Potassium 200mg-28.5mg/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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