FDA label 84e8333d-4eab-4ae5-8fa2-e08b668123df

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

SPL set ID
9d3f66e4-ef19-4341-a19f-3d3d0786fbfc
SPL ID
84e8333d-4eab-4ae5-8fa2-e08b668123df
Version
2
Effective date
2011-06-07
Source export date
2026-08-01
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-01/29baabee7fa6726d72190670d84f1571113181a958a8119cbe97e8f0d1d955b2/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:16:36

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS Serious adverse reactions associated with the administration of intravenous dipyridamole have included cardiac death, fatal and non-fatal myocardial infarction, ventricular fibrillation, symptomatic ventricular tachycardia, stroke, transient cerebral ischemia, seizures, anaphylactoid reaction, and bronchospasm. There have been reported cases of asystole, sinus node arrest, sinus node depression and conduction block. Patients with abnormalities of cardiac impulse formation/conduction or severe coronary artery disease may be at increased risk for these events. In a study of 3911 patients given intravenous dipyridamole as an adjunct to thallium myocardial perfusion imaging, two types of serious adverse events were reported: 1) four cases of myocardial infarction (0.1%), two fatal (0.05%) and two non-fatal (0.05%); and 2) six cases of severe bronchospasm (0.2%). Although the incidence of these serious adverse events was small (0.3%, 10 of 3911), the potential clinical information to be gained through use of intravenous dipyridamole thallium imaging (see INDICATION AND USAGE noting the rate of false positive and false negative results) must be weighed against the risk to the patient. Patients with a history of unstable angina may be at a greater risk for severe myocardial ischemia. Patients with a history of asthma may be at a greater risk for bronchospasm during dipyridamole injection use. When thallium myocardial perfusion imaging is performed with intravenous dipyridamole, parenteral aminophylline should be readily available for relieving adverse events such as bronchospasm or chest pain. Vital signs should be monitored during, and for 10–15 minutes following, the intravenous infusion of dipyridamole and an electrocardiographic tracing should be obtained using at least one chest lead. Should severe chest pain or bronchospasm occur, parenteral aminophylline may be administered by slow intravenous injection (50–100 mg over 30–60 seconds) in doses ranging from 50 to 250 mg. In the case of severe hypotension, the patient should be placed in a supine position with the head tilted down if necessary, before administration of parenteral aminophylline. If 250 mg of aminophylline does not relieve chest pain symptoms within a few minutes, sublingual nitroglycerin may be administered. If chest pain continues despite use of aminophylline and nitroglycerin, the possibility of myocardial infarction should be considered. If the clinical condition of a patient with an adverse event permits a one minute delay in the administration of parenteral aminophylline, thallium-201 may be injected and allowed to circulate for one minute before the injection of aminophylline. This will allow initial thallium perfusion imaging to be performed before reversal of the pharmacologic effects of dipyridamole injection on the coronary circulation.

Adverse reactions cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Adverse reactions sections page 1 of 1 · 2 matching rows.

adverse reactions

ADVERSE REACTIONS Adverse reaction information concerning intravenous dipyridamole is derived from a study of 3911 patients in which intravenous dipyridamole was used as an adjunct to thallium myocardial perfusion imaging and from spontaneous reports of adverse reactions and the published literature. Serious adverse events (cardiac death, fatal and non-fatal myocardial infarction, ventricular fibrillation, asystole, sinus node arrest, symptomatic ventricular tachycardia, stroke, transient cerebral ischemia, seizures, anaphylactoid reaction and bronchospasm) are described above. (See WARNINGS ). In the study of 3911 patients, the most frequent adverse reactions were: chest pain/angina pectoris (19.7%), electrocardiographic changes (most commonly ST-T changes) (15.9%), headache (12.2%), and dizziness (11.8%). Adverse reactions occurring in greater than 1% of the patients in the study are shown in the following table: Incidence (%) of Drug-Related Adverse Events Chest pain/angina pectoris 19.7 Headache 12.2 Dizziness 11.8 Electrocardiographic Abnormalities/ST-T changes 7.5 Electrocardiographic Abnormalities/Extrasystoles 5.2 Hypotension 4.6 Nausea 4.6 Flushing 3.4 Electrocardiographic Abnormalities/Tachycardia 3.2 Dyspnea 2.6 Pain Unspecified 2.6 Blood Pressure Lability 1.6 Hypertension 1.5 Paresthesia 1.3 Fatigue 1.2 Less common adverse reactions occurring in 1% or less of the patients within the study included: Cardiovascular System Electrocardiographic abnormalities unspecified (0.8%), arrhythmia unspecified (0.6%), palpitation (0.3%), ventricular tachycardia (0.2%, see WARNINGS ), bradycardia (0.2%), myocardial infarction (0.1%, see WARNINGS ), AV block (0.1%), syncope (0.1%), orthostatic hypotension (0.1%), atrial fibrillation (0.1%), supraventricular tachycardia (0.1%), ventricular arrhythmia unspecified (0.03%, see WARNINGS ), heart block unspecified (0.03%), cardiomyopathy (0.03%), edema (0.03%). Central and Peripheral Nervous System Hypothesia (0.5%), hypertonia (0.3%), nervousness/anxiety (0.2%), tremor (0.1%), abnormal coordination (0.03%), somnolence (0.03%), dysphonia (0.03%), migraine (0.03%), vertigo (0.03%). Gastrointestinal System Dyspepsia (1.0%), dry mouth (0.8%), abdominal pain (0.7%), flatulence (0.6%), vomiting (0.4%), eructation (0.1%), dysphagia (0.03%), tenesmus (0.03%), appetite increased (0.03%). Respiratory System Pharyngitis (0.3%), bronchospasm (0.2%, see WARNINGS ), hyperventilation (0.1%), rhinitis (0.1%), coughing (0.03%), pleural pain (0.03%). Other Myalgia (0.9%), back pain (0.6%), injection site reaction unspecified (0.4%), diaphoresis (0.4%), asthenia (0.3%), malaise (0.3%), arthralgia (0.3%), injection site pain (0.1%), rigor (0.1%), earache (0.1%), tinnitus (0.1%), vision abnormalities unspecified (0.1%), dysgeusia (0.1%), thirst (0.03%), depersonalization (0.03%), eye pain (0.03%), renal pain (0.03%), perineal pain (0.03%), breast pain (0.03%), intermittent claudication (0.03%), leg cramping (0.03%). In additional postmarketing experience, there have been rare reports of allergic reaction including urticaria, pruritus, dermatitis and rash.

adverse reactions table

<table width="70%"> <col width="70%" align="left" valign="top"/> <col width="30%" align="center" valign="top"/> <thead> <tr> <th/> <th>Incidence (%) of Drug-Related Adverse Events</th> </tr> </thead> <tbody> <tr> <td>Chest pain/angina pectoris</td> <td>19.7</td> </tr> <tr> <td>Headache</td> <td>12.2</td> </tr> <tr> <td>Dizziness</td> <td>11.8</td> </tr> <tr> <td colspan="2">Electrocardiographic</td> </tr> <tr> <td> Abnormalities/ST-T changes</td> <td>7.5</td> </tr> <tr> <td colspan="2">Electrocardiographic</td> </tr> <tr> <td> Abnormalities/Extrasystoles</td> <td>5.2</td> </tr> <tr> <td>Hypotension</td> <td>4.6</td> </tr> <tr> <td>Nausea</td> <td>4.6</td> </tr> <tr> <td>Flushing</td> <td>3.4</td> </tr> <tr> <td colspan="2">Electrocardiographic</td> </tr> <tr> <td> Abnormalities/Tachycardia</td> <td>3.2</td> </tr> <tr> <td>Dyspnea</td> <td>2.6</td> </tr> <tr> <td>Pain Unspecified</td> <td>2.6</td> </tr> <tr> <td>Blood Pressure Lability</td> <td>1.6</td> </tr> <tr> <td>Hypertension</td> <td>1.5</td> </tr> <tr> <td>Paresthesia</td> <td>1.3</td> </tr> <tr> <td>Fatigue</td> <td>1.2</td> </tr> </tbody> </table>