Dipyridamole

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)

Brand name
Dipyridamole
Generic name
DIPYRIDAMOLE
Manufacturer
REMEDYREPACK INC.
Product type
HUMAN PRESCRIPTION DRUG
SPL set ID
226099e2-70bb-4b9b-bb52-c20fbca2aec5
SPL ID
509b6d30-eda6-417e-e063-6294a90a4a94
Version
1
Effective date
2026-04-29
Source export date
2026-09-28
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:19:12
Harmonized routes table
Harmonized routes
ORAL

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 reactions at therapeutic doses are usually minimal and transient. On long-term use of dipyridamole 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/ Placebo/ Warfarin Warfarin Number of patients 147 170 Dizziness 13.6% 8.2% Abdominal distress 6. 1% 3.5% Headache 2.3% 0.0% 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 post-marketing 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.

adverse reactions table

<table ID="ID44" width="426" styleCode="Noautorules"><caption>Table 1 Adverse Reactions Reported in 2 Heart Valve Replacement Trials</caption><col width="145"/><col width="183"/><col width="98"/><tbody><tr><td align="left" styleCode="Lrule Toprule Rrule" valign="top"><content styleCode="bold">Adverse Reaction</content> </td><td align="center" styleCode=" Toprule Rrule" valign="top"><content styleCode="bold">Dipyridamole Tablets/</content> </td><td align="center" styleCode=" Toprule Rrule" valign="top"><content styleCode="bold">Placebo/</content> </td></tr><tr><td align="left" styleCode="Lrule Botrule Rrule" valign="top"> </td><td align="center" styleCode=" Botrule Rrule" valign="top"><content styleCode="bold">Warfarin</content> </td><td align="center" styleCode=" Botrule Rrule" valign="top"><content styleCode="bold">Warfarin</content> </td></tr><tr><td align="left" styleCode=" Lrule Rrule" valign="top">Number of patients </td><td align="center" styleCode=" Rrule" valign="top">147 </td><td align="center" styleCode=" Rrule" valign="top">170 </td></tr><tr><td align="left" styleCode=" Lrule Rrule" valign="top">Dizziness </td><td align="center" styleCode=" Rrule" valign="top">13.6% </td><td align="center" styleCode=" Rrule" valign="top">8.2% </td></tr><tr><td align="left" styleCode=" Lrule Rrule" valign="top">Abdominal distress </td><td align="center" styleCode=" Rrule" valign="top">6. 1% </td><td align="center" styleCode=" Rrule" valign="top">3.5% </td></tr><tr><td align="left" styleCode=" Lrule Rrule" valign="top">Headache </td><td align="center" styleCode=" Rrule" valign="top">2.3% </td><td align="center" styleCode=" Rrule" valign="top">0.0% </td></tr><tr><td align="left" styleCode="Lrule Botrule Rrule" valign="top">Rash </td><td align="center" styleCode=" Botrule Rrule" valign="top">2.3% </td><td align="center" styleCode=" Botrule Rrule" valign="top">1.1% </td></tr></tbody></table>

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.