Aceon Oral Tablet 2Mg Drug Medication Dosage Information
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Aceon: Oral tablet (2mg)

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Drug Image file DrugItem_4762.JPG
Aceon 2mg Tab
AbbVie US LLC
Pill Identification: ACN 2  |  SLV SLV

What is this Medicine?

PERINDOPRIL (per IN doe pril) is an ACE inhibitor. This medicine is used to treat high blood pressure. This medicine is also used in patients with coronary artery disease. It may reduce the risk of heart attack in these patients.

In-Depth Information
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Aceon 2mg Tablet

NDC: 000321101
  • Prescription Required
  • Not a Controlled Drug
    (CSA Schedule)
  • FDA Approved




FDA approved for the following conditions:
Reduction Of Cardiovascular Mortality, Myocardial Infarction Prophylaxis, Hypertension

Sometimes used for but not FDA approved for the following conditions:
Heart Failure

Storage Information
Protect from moisture
Store at controlled room temperature (between 68 and 77 degrees F)
Aceon 2mg Tablet
Drug Image file DrugItem_4762.JPG
AbbVie US LLC
Pill Identification: ACN 2  |  SLV SLV
Shape: oblong
Color: white

Reported Side Effects for Aceon 2mg Tablet

Anemia Incidence:
<1.0%*
Severity: MODERATE
Onset: DELAYED
Liver Infection Incidence:
<1.0%*
Severity: MODERATE
Onset: DELAYED
Liver Failure Incidence:
<1.0%*
Severity: SEVERE
Onset: DELAYED
Death Of Liver Tissue Incidence:
<1.0%*
Severity: SEVERE
Onset: DELAYED
Pancytopenia Incidence:
<1.0%*
Severity: SEVERE
Onset: DELAYED
Kidney Failure Incidence:
<1.0%*
Severity: SEVERE
Onset: DELAYED
Low Platelet Count Incidence:
<1.0%*
Severity: MODERATE
Onset: DELAYED
Angioedema Incidence:
<1.0%*
Severity: SEVERE
Onset: RAPID
No White Blood Cells Incidence:
<1.0%*
Severity: SEVERE
Onset: DELAYED
Low White Blood Cells Incidence:
0.1%*
Severity: MODERATE
Onset: DELAYED
Low White Blood Cell Counts Incidence:
0.1%*
Severity: MODERATE
Onset: DELAYED
Low Blood Pressure Incidence:
0.3-0.8%*
Severity: MILD
Onset: EARLY
Elevated Hepatic Enzymes Incidence:
0.5-1.6%*
Severity: MODERATE
Onset: DELAYED
Postural Low Blood Pressure Incidence:
0.8%*
Severity: MODERATE
Onset: DELAYED
Back Pain Incidence:
5.8%*
Severity: MILD
Onset: DELAYED
Lightheadedness Incidence:
8.2%*
Severity: MILD
Onset: EARLY
Cough Incidence:
12.0%*
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 D - Adequate well-controlled or observational studies in pregnant women have demonstrated a risk to the fetus. However, the benefits of therapy may outweigh the potential risk. For example, the drug may be acceptable if needed in a life-threatening situation or serious disease for which safer drugs cannot be used or are ineffective.

Second Trimester

Class D - Adequate well-controlled or observational studies in pregnant women have demonstrated a risk to the fetus. However, the benefits of therapy may outweigh the potential risk. For example, the drug may be acceptable if needed in a life-threatening situation or serious disease for which safer drugs cannot be used or are ineffective.

Third Trimester

Class D - Adequate well-controlled or observational studies in pregnant women have demonstrated a risk to the fetus. However, the benefits of therapy may outweigh the potential risk. For example, the drug may be acceptable if needed in a life-threatening situation or serious disease for which safer drugs cannot be used or are ineffective.

Lactation

Caution - Not enough information is available to rule out harm to infants when this drug is taken by nursing mothers.


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