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Medical Information
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EKR Corporate

 

Medical Information

Healthcare professionals and patients can request specific medical information, report adverse events, or provide feedback about Ready-to-Use CARDENE I.V. by contacting the Medical Information Department:

Phone: 877-207-5802

Email: medinfo@ekrtx.com

Mail: EKR Therapeutics, Inc.
1545 US Highway 206, 3rd Floor
Bedminster, NJ 07921

FAX: 866-457-0803

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Contact a Representative

To have a local sales representative contact you:

Email: medinfo@ekrtx.com

Phone: 877-207-5802

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EKR Corporate

Mail: EKR Therapeutics, Inc.
1545 US Highway 206, 3rd Floor
Bedminster, NJ 07921

Phone: 877-435-2524

View our Terms of Use.

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Important Safety Information
Close monitoring of the blood pressure is required during therapy. CARDENE I.V. is contraindicated in patients with known hypersensitivity to the drug and in patients with advanced aortic stenosis. Reduction of diastolic pressure and reduced afterload may worsen rather than improve myocardial oxygen balance. Caution is advised when administering CARDENE I.V. to patients with impaired renal or hepatic function, in combination with a beta-blocker in patients with congestive heart failure, or portal hypertension. Observe caution in patients with significant left ventricular dysfunction due to possible negative inotropic effect. CARDENE I.V. gives no protection against the dangers of abrupt beta-blocker withdrawal; beta-blocker dosage should be gradually reduced. Levels of cyclosporine should be closely monitored during therapy. The most common side effects of CARDENE I.V. are headache (14.6%), hypotension (5.6%), nausea/vomiting (4.9%), and tachycardia (3.5%). Less frequent adverse effects, in each case occurring at 1.4%, include ECG abnormalities, postural hypotension, ventricular extrasystoles, injection-site reaction, dizziness, sweating and polyuria.

Please see full prescribing information.

 

© EKR Therapeutics, Inc. All rights reserved. August 2009.