Dipyridamole

Pronunciation

Dosage Form: tablet, film coated

Dipyridamole TABLETS, USP

Rx only

Dipyridamole Description

Dipyridamole USP is a platelet inhibitor chemically described as 2,2',2'',2'''-[(4,8-Dipiperidinopyrimido[5,4-d]pyrimidine-2,6-diyl)dinitrilo]-tetraethanol. It has the following structural formula:

C24H40N8O4 M.W. 504.63

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Dipyridamole is an odorless yellow crystalline powder, having a bitter taste. It is soluble in dilute acids, methanol and chloroform, and practically insoluble in water.

Each Dipyridamole tablet USP, for oral administration, contains 25 mg, 50 mg, or 75 mg Dipyridamole, USP and contains the following inactive ingredients: colloidal silicon dioxide, hypromellose, lactose anhydrous, magnesium stearate, microcrystalline cellulose, polyethylene glycol, polysorbate 80, propylene glycol, stearic acid, sodium starch glycolate, and titanium dioxide.

Dipyridamole - Clinical Pharmacology

It is believed that platelet reactivity and interaction with prosthetic cardiac valve surfaces, resulting in abnormally shortened platelet survival time, is a significant factor in thromboembolic complications occurring in connection with prosthetic heart valve replacement.

Dipyridamole USP tablets have been found to lengthen abnormally shortened platelet survival time in a dose-dependent manner.

In three randomized controlled clinical trials involving 854 patients who had undergone surgical placement of a prosthetic heart valve, Dipyridamole tablets, in combination with warfarin, decreased the incidence of postoperative thromboembolic events by 62 to 91% compared to warfarin treatment alone. The incidence of thromboembolic events in patients receiving the combination of Dipyridamole tablets and warfarin ranged from 1.2 to 1.8%. In three additional studies involving 392 patients taking Dipyridamole tablets and coumarin-like anticoagulants, the incidence of thromboembolic events ranged from 2.3 to 6.9%.

In these trials, the coumarin anticoagulant was begun between 24 hours and 4 days postoperatively, and the Dipyridamole tablets were begun between 24 hours and 10 days postoperatively. The length of follow-up in these trials varied from 1 to 2 years.

Dipyridamole tablets do not influence prothrombin time or activity measurements when administered with warfarin.

Mechanism of Action

Dipyridamole inhibits the uptake of adenosine into platelets, endothelial cells and erythrocytes in vitro and in vivo; the inhibition occurs in a dose-dependent manner at therapeutic concentrations (0.5 to 1.9 mcg/mL). This inhibition results in an increase in local concentrations of adenosine which acts on the platelet A2-receptor thereby stimulating platelet adenylate cyclase and increasing platelet cyclic-3',5'-adenosine monophosphate (cAMP) levels. Via this mechanism, platelet aggregation is inhibited in response to various stimuli such as platelet activating factor (PAF), collagen and adenosine diphosphate (ADP).

Dipyridamole inhibits phosphodiesterase (PDE) in various tissues. While the inhibition of cAMP-PDE is weak, therapeutic levels of Dipyridamole inhibit cyclic-3',5'-guanosine monophosphate-PDE (cGMP-PDE), thereby augmenting the increase in cGMP produced by EDRF (endothelium-derived relaxing factor, now identified as nitric oxide).

Hemodynamics

In dogs intraduodenal doses of Dipyridamole of 0.5 to 4 mg/kg produced dose-related decreases in systemic and coronary vascular resistance leading to decreases in systemic blood pressure and increases in coronary blood flow. Onset of action was in about 24 minutes and effects persisted for about 3 hours.

Similar effects were observed following IV Dipyridamole in doses ranging from 0.025 to 2 mg/kg.

In man the same qualitative hemodynamic effects have been observed. However, acute intravenous administration of Dipyridamole may worsen regional myocardial perfusion distal to partial occlusion of coronary arteries.

Pharmacokinetics and Metabolism

Following an oral dose of Dipyridamole tablets, the average time to peak concentration is about 75 minutes. The decline in plasma concentration following a dose of Dipyridamole tablets fits a two-compartment model. The alpha half-life (the initial decline following peak concentration) is approximately 40 minutes. The beta half-life (the terminal decline in plasma concentration) is approximately 10 hours. Dipyridamole is highly bound to plasma proteins. It is metabolized in the liver where it is conjugated as a glucuronide and excreted with the bile.

Indications and Usage for Dipyridamole

Dipyridamole USP tablets are indicated as an adjunct to coumarin anticoagulants in the prevention of postoperative thromboembolic complications of cardiac valve replacement.

Contraindications

Hypersensitivity to Dipyridamole and any of the other components.

Precautions

General

Coronary Artery Disease

Dipyridamole has a vasodilatory effect and should be used with caution in patients with severe coronary artery disease (e.g., unstable angina or recently sustained myocardial infarction). Chest pain may be aggravated in patients with underlying coronary artery disease who are receiving Dipyridamole.

Hepatic Insufficiency

Elevations of hepatic enzymes and hepatic failure have been reported in association with Dipyridamole administration.

Hypotension

Dipyridamole should be used with caution in patients with hypotension since it can produce peripheral vasodilation.

Laboratory Tests

Dipyridamole has been associated with elevated hepatic enzymes.

Drug Interactions

No pharmacokinetic drug-drug interaction studies were conducted with Dipyridamole USP tablets. The following information was obtained from the literature.

Adenosine

Dipyridamole has been reported to increase the plasma levels and cardiovascular effects of adenosine. Adjustment of adenosine dosage may be necessary.

Cholinesterase Inhibitors

Dipyridamole may counteract the anticholinesterase effect of cholinesterase inhibitors, thereby potentially aggravating myasthenia gravis.

Carcinogenesis, Mutagenesis, Impairment of Fertility

In studies in which Dipyridamole was administered in the feed to mice (up to 111 weeks in males and females) and rats (up to 128 weeks in males and up to 142 weeks in females), there was no evidence of drug related carcinogenesis. The highest dose administered in these studies (75 mg/kg/day) was, on a mg/m2 basis, about equivalent to the maximum recommended daily human oral dose (MRHD) in mice and about twice the MRHD in rats. Mutagenicity tests of Dipyridamole with bacterial and mammalian cell systems were negative. There was no evidence of impaired fertility when Dipyridamole was administered to male and female rats at oral doses up to 500 mg/kg/day (about 12 times the MRHD on a mg/m2 basis). A significant reduction in number of corpora lutea with consequent reduction in implantations and live fetuses was, however, observed at 1250 mg/kg (more than 30 times the MRHD on a mg/m2 basis).

Pregnancy

Teratogenic Effects

Pregnancy Category B

Reproduction studies have been performed in mice, rabbits and rats at oral Dipyridamole doses of up to 125 mg/kg, 40 mg/kg and 1000 mg/kg, respectively (about 1½, 2 and 25 times the maximum recommended daily human oral dose, respectively, on a mg/m2 basis) and have revealed no evidence of harm to the fetus due to Dipyridamole. There are, however, no adequate and well-controlled studies in pregnant women. Because animal reproduction studies are not always predictive of human response, Dipyridamole should be used during pregnancy only if clearly needed.

Nursing Mothers

As Dipyridamole is excreted in human milk, caution should be exercised when Dipyridamole tablets are administered to a nursing woman.

Pediatric Use

Safety and effectiveness in the pediatric population below the age of 12 years has not been established.

Adverse Reactions

Adverse reactions at therapeutic doses are usually minimal and transient. On long-term use of Dipyridamole USP tablets initial side effects usually disappear. The following reactions in Table 1 were reported in two heart valve replacement trials comparing Dipyridamole tablets and warfarin therapy to either warfarin alone or warfarin and placebo:

Table 1: Adverse Reactions Reported in 2 Heart Valve Replacement Trials
Adverse Reaction Dipyridamole Tablets/ Warfarin Placebo/Warfarin
Number of patients 147 170
Dizziness 13.6% 8.2%
Abdominal distress 6.1% 3.5%
Headache 2.3% 0%
Rash 2.3% 1.1%

Other reactions from uncontrolled studies include diarrhea, vomiting, flushing and pruritus. In addition, angina pectoris has been reported rarely, and there have been rare reports of liver dysfunction. On those uncommon occasions when adverse reactions have been persistent or intolerable, they have ceased on withdrawal of the medication.

When Dipyridamole tablets were administered concomitantly with warfarin, bleeding was no greater in frequency or severity than that observed when warfarin was administered alone. In rare cases, increased bleeding during or after surgery has been observed.

In postmarketing reporting experience, there have been rare reports of hypersensitivity reactions (such as rash, urticaria, severe bronchospasm, and angioedema), larynx edema, fatigue, malaise, myalgia, arthritis, nausea, dyspepsia, paresthesia, hepatitis, thrombocytopenia, alopecia, cholelithiasis, hypotension, palpitation, and tachycardia.

Overdosage

In case of real or suspected overdose, seek medical attention or contact a Poison Control Center immediately. Careful medical management is essential. Based upon the known hemodynamic effects of Dipyridamole, symptoms such as warm feeling, flushes, sweating, restlessness, feeling of weakness and dizziness may occur. A drop in blood pressure and tachycardia might also be observed.

Symptomatic treatment is recommended, possibly including a vasopressor drug. Gastric lavage should be considered. Administration of xanthine derivatives (e.g., aminophylline) may reverse the hemodynamic effects of Dipyridamole overdose. Since Dipyridamole is highly protein bound, dialysis is not likely to be of benefit.

Dipyridamole Dosage and Administration

Adjunctive Use In Prophylaxis Of Thromboembolism After Cardiac Valve Replacement

The recommended dose is 75 to 100 mg four times daily as an adjunct to the usual warfarin therapy. Please note that aspirin is not to be administered concomitantly with coumarin anticoagulants.

How is Dipyridamole Supplied

Dipyridamole Tablets USP, 25 mg are available as white, round, film-coated, unscored, biconvex tablets, debossed with "252" on one side and stylized b on the other side, available in bottles of 100 and 1000 tablets.

Dipyridamole Tablets USP, 50 mg are available as white, round, film-coated, unscored, biconvex tablets, debossed with "285" on one side and stylized b on the other side, available in bottles of 100 and 1000 tablets.

Dipyridamole Tablets USP, 75 mg are white, round, film-coated, unscored, biconvex tablet. Debossed "286" on one side and "BARR" on the other side, available in bottles of 100 and 1000 tablets.

Store at 20º to 25ºC (68º to 77ºF) [See USP Controlled Room Temperature].

Dispense with a tight, light-resistant container as defined in the USP, with a child-resistant closure (as required).

KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN.

TEVA PHARMACEUTICALS USA

Sellersville, PA 18960

Iss. 2/2011

PRINCIPAL DISPLAY PANEL

Dipyridamole Tablets USP 25mg 100s Label Text

NDC 0555-0252-02

Dipyridamole
Tablets USP
25 mg

Rx only

100 TABLETS

TEVA

PRINCIPAL DISPLAY PANEL

Dipyridamole Tablets USP 50mg 100s Label Text

NDC 0555-0285-02

Dipyridamole
Tablets USP
50 mg

Rx only

100 TABLETS

TEVA

PRINICIPAL DISPLAY PANEL

Dipyridamole Tablets USP 75 mg 100s Label Text

NDC 0555-0286-02

Dipyridamole
Tablets USP
75 mg

Rx only

100 TABLETS

TEVA

Dipyridamole 
Dipyridamole tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:0555-0252
Route of Administration ORAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Dipyridamole (Dipyridamole) Dipyridamole 25 mg
Inactive Ingredients
Ingredient Name Strength
SILICON DIOXIDE  
HYPROMELLOSE 2910 (3 MPA.S)  
HYPROMELLOSE 2910 (6 MPA.S)  
ANHYDROUS LACTOSE  
MAGNESIUM STEARATE  
CELLULOSE, MICROCRYSTALLINE  
POLYETHYLENE GLYCOLS  
POLYSORBATE 80  
PROPYLENE GLYCOL  
STEARIC ACID  
SODIUM STARCH GLYCOLATE TYPE A POTATO  
TITANIUM DIOXIDE  
Product Characteristics
Color WHITE Score no score
Shape ROUND Size 6mm
Flavor Imprint Code b;252
Contains         
Packaging
# Item Code Package Description
1 NDC:0555-0252-02 100 TABLET, FILM COATED in 1 BOTTLE
2 NDC:0555-0252-05 1000 TABLET, FILM COATED in 1 BOTTLE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA087184 10/01/1980
Dipyridamole 
Dipyridamole tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:0555-0285
Route of Administration ORAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Dipyridamole (Dipyridamole) Dipyridamole 50 mg
Inactive Ingredients
Ingredient Name Strength
SILICON DIOXIDE  
HYPROMELLOSE 2910 (3 MPA.S)  
HYPROMELLOSE 2910 (6 MPA.S)  
ANHYDROUS LACTOSE  
CELLULOSE, MICROCRYSTALLINE  
MAGNESIUM STEARATE  
POLYETHYLENE GLYCOLS  
POLYSORBATE 80  
PROPYLENE GLYCOL  
STEARIC ACID  
SODIUM STARCH GLYCOLATE TYPE A POTATO  
TITANIUM DIOXIDE  
Product Characteristics
Color WHITE Score no score
Shape ROUND Size 7mm
Flavor Imprint Code b;285
Contains         
Packaging
# Item Code Package Description
1 NDC:0555-0285-02 100 TABLET, FILM COATED in 1 BOTTLE
2 NDC:0555-0285-05 1000 TABLET, FILM COATED in 1 BOTTLE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA087716 01/01/1982
Dipyridamole 
Dipyridamole tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:0555-0286
Route of Administration ORAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Dipyridamole (Dipyridamole) Dipyridamole 75 mg
Inactive Ingredients
Ingredient Name Strength
SILICON DIOXIDE  
HYPROMELLOSE 2910 (3 MPA.S)  
HYPROMELLOSE 2910 (6 MPA.S)  
ANHYDROUS LACTOSE  
MAGNESIUM STEARATE  
CELLULOSE, MICROCRYSTALLINE  
POLYETHYLENE GLYCOLS  
POLYSORBATE 80  
PROPYLENE GLYCOL  
STEARIC ACID  
SODIUM STARCH GLYCOLATE TYPE A POTATO  
TITANIUM DIOXIDE  
Product Characteristics
Color WHITE Score no score
Shape ROUND Size 9mm
Flavor Imprint Code BARR;286
Contains         
Packaging
# Item Code Package Description
1 NDC:0555-0286-02 100 TABLET, FILM COATED in 1 BOTTLE
2 NDC:0555-0286-05 1000 TABLET, FILM COATED in 1 BOTTLE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA087717 01/01/1982
Labeler - Barr Laboratories Inc. (802716563)
Revised: 10/2013
 
Barr Laboratories Inc.
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