Air Polymer-Type A — Active Pharmaceutical Ingredient

Air Polymer-Type A is an active pharmaceutical ingredient found in 1 FDA-approved drug product. Forms: FOAM. Routes: INTRAUTERINE.

This content is for informational purposes only. Always consult a healthcare professional.

Air Polymer-Type A (1 brand name, 1 dosage form, 1 route)

Available dosage forms: FOAM.

Routes of administration: INTRAUTERINE.

Brand Names

  • EXEM FOAM KIT

Indications and Usage

ExEm ® Foam is indicated for sonohysterosalpingography to assess fallopian tube patency in women with known or suspected infertility.

Contraindications

ExEm Foam is contraindicated for use in: Pregnancy [see Warnings and Precautions (5.1)] . Patients with known or suspected lower genital tract inflammation or infection [see Warnings and Precautions (5.2)]. Patients who have had a gynecologic procedure within the last 30 days [see Warnings and Precautions (5.2)]. Patients with vaginal bleeding Due to the risk of intravasation of ExEm Foam as a result of exposure of the endometrial vessels during bleeding, and Due to the potential risk of endometriosis as a result of seeding the peritoneum with endometrial tissue. Patients with known or suspected reproductive tract neoplasia due to the risk of peritoneal spread of neoplasm .

Mechanism of Action

ExEm Foam (air polymer-type A) intrauterine foam is formed by mixing the clear Gel [polymer-type A (hydroxyethyl cellulose), glycerin, and purified water] with air and Sterile Purified Water, creating an echogenic contrast agent. When visualized with ultrasound, the foam appears echogenic or bright within the fallopian tubes and peritoneal cavity.

⚠ Caution
Medical Disclaimer: This information is for educational purposes only. Always consult a healthcare professional before taking any medication.