Dipyridamole Oral Tablet 25Mg Drug Medication Dosage Information
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Dipyridamole: Oral tablet (25mg)

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Drug Image file DrugItem_3844.JPG
Dipyridamole 25mg Tab
Barr Laboratories Inc a Division of Teva USA
Pill Identification: b  |  252
Drug Image file DrugItem_11594.JPG
Dipyridamole 25mg Tab
Zydus Pharmaceuticals (USA) Inc
Pill Identification: ZE 43 
Drug Image file default-drug-image.png
Dipyridamole 25mg Tab

What is this Medicine?

DIPYRIDAMOLE (dye peer ID a mole) is used in patients who have had heart valve replacements. It prevents blood clots and reduces the risk of complications.

CVS Pharmacy Patient Statistics for Dipyridamole: Oral tablet(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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Dipyridamole 25mg Tablet

NDC: 005550252
  • Prescription Required
  • Not a Controlled Drug
    (CSA Schedule)
  • FDA Approved




FDA approved for the following conditions:
Arterial Thromboembolism Prophylaxis, Prosthetic Heart Valves

Sometimes used for but not FDA approved for the following conditions:
Valvular Heart Disease, Myocardial Infarction Prophylaxis, Transient Ischemic Attack (TIA), Proteinuria, Cardiomyopathy

Storage Information
Store at room temperature (between 59 to 86 degrees F)
Dipyridamole 25mg Tablet
Drug Image file DrugItem_3844.JPG
Barr Laboratories Inc a Division of Teva USA
Pill Identification: b  |  252
Shape: round
Color: white

Reported Side Effects for Dipyridamole 25mg Tablet

Headache Incidence:
<12.2%*
Severity: MILD
Onset: EARLY
Drowsiness Incidence:
<0.1%*
Severity: MILD
Onset: EARLY
Breathing Difficulties Incidence:
0.2%*
Severity: SEVERE
Onset: RAPID
Feeling Sick Incidence:
0.3%*
Severity: MILD
Onset: EARLY
Rapid Heart Rate Incidence:
0.3%*
Severity: MODERATE
Onset: EARLY
Joint Pain Incidence:
0.3%*
Severity: MILD
Onset: DELAYED
Vomiting Incidence:
0.4%*
Severity: MILD
Onset: EARLY
Stomach Pain Incidence:
0.7-6.1%*
Severity: MILD
Onset: EARLY
Muscle Pain Incidence:
0.9%*
Severity: MILD
Onset: EARLY
Upset Stomach Incidence:
1.0%*
Severity: MILD
Onset: EARLY
Tired Incidence:
1.2%*
Severity: MILD
Onset: EARLY
Paresthesias Incidence:
1.3%*
Severity: MILD
Onset: DELAYED
Skin Rash Incidence:
2.3%*
Severity: MILD
Onset: EARLY
Rapid Heart Rate Incidence:
3.2%*
Severity: MODERATE
Onset: RAPID
Low Blood Pressure Incidence:
4.6%*
Severity: MODERATE
Onset: RAPID
Upset Stomach Incidence:
4.6%*
Severity: MILD
Onset: EARLY
Lightheadedness Incidence:
11.8-13.6%*
Severity: MILD
Onset: EARLY
*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

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


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Patient Experiences with Dipyridamole

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