"Coadministration of tetanus toxoid, reduced diphtheria toxoid, and acellular pertussis (Tdap) and influenza vaccines in pregnant women does not appear to raise the risk for medically attended adverse acute outcomes or birth outcomes compared with"...
- PROSTIN E2 Vaginal Suppository is indicated for the termination of pregnancy from the 12th through the 20th gestational week as calculated from the first day of the last normal menstrual period.
- PROSTIN E2 is also indicated for evacuation of the uterine contents in the management of missed abortion or intrauterine fetal death up to 28 weeks of gestational age as calculated from the first day of the last normal menstrual period.
- PROSTIN E2 is indicated in the management of nonmetastatic gestational trophoblastic disease (benign hydatidiform mole).
DOSAGE AND ADMINISTRATION
STORE IN A FREEZER NOT ABOVE -20°C (-4°F) BUT BRING TO ROOM TEMPERATURE JUST PRIOR TO USE.
REMOVE FOIL BEFORE USE.
Additional intravaginal administration of each subsequent suppository should be at 3- to 5-hour intervals until abortion occurs. Within the above recommended intervals administration time should be determined by abortifacient progress, uterine contractility response, and by patient tolerance. Continuous administration of the drug for more than 2 days is not recommended.
PROSTIN E2 Vaginal Suppositories are available in foil strips of 5 individually sealed suppositories, NDC 0009-0827-03. Each suppository contains 20 mg of dinoprostone in a mixture of glycerides of fatty acids.
STORE IN A FREEZER NOT ABOVE -20°C (-4°F).
This product's label may have been updated. For current full prescribing information, please visit www.pfizer.com
Distributed by: Pharmacia & Upjohn Co., Division of Pfizer Inc., New York NY, 10017. Revised: Dec 2014This monograph has been modified to include the generic and brand name in many instances.
Last reviewed on RxList: 6/13/2016
Additional Prostin E2 Information
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