Pfizer for Professionals Pfizer for Professionals




Pfizer Medical Information
(Search Medical Responses)
WyethHCP.com
(Access Wyeth for Professionals)
Explore Other Online Resources
ppn-vr-sso-links.htm
To report an adverse event or to speak to a member of Pfizer Medical Information, please call 1-800-438-1985

Share Your Feedback
Prescribing Information
CAVERJECT IMPULSE® Dual Chamber System alprostadil for injection
Overdosage
Return to the CAVERJECT IMPULSE Product Center

Overdosage was not observed in clinical trials with CAVERJECT. If intracavernous overdose of CAVERJECT occurs, the patient should be under medical supervision until any systemic effects have resolved and/or until penile detumescence has occurred. Symptomatic treatment of any systemic symptoms would be appropriate.


CAVERJECT IMPULSE Safety Information
 

Important Safety Information

CAVERJECT IMPULSE is indicated for the treatment of erectile dysfunction due to neurogenic, vasculogenic, psychogenic, or mixed etiology.

The most common side effect of CAVERJECT IMPULSE was penile pain, reported by 37% of patients in clinical studies. Only 3% discontinued CAVERJECT IMPULSE for this reason.

CAVERJECT IMPULSE should not be used in men hypersensitive to alprostadil, men with conditions that may predispose them to priapism, men with anatomical deformities of the penis, men with penile implants, or men for whom sexual activity is not advisable or is contraindicated. Penile fibrosis, including Peyronie's disease, was reported in clinical trials with CAVERJECT IMPULSE.

Patients should be instructed to report any erection lasting 4 hours or longer. Treatment of priapism should not be delayed more than 6 hours.

Each patient should be titrated to the lowest effective dose.

The product information in this site is intended only for residents of the United States.

caverject_impulse_safety_information.htm
SetPProProdListVar.htm
SetPFPGroupVar.htm