ARESTIN® Student Access is a program, sponsored by OraPharma, Inc., the makers of ARESTIN® (minocycline HCI) Microspheres, 1mg, and designed with the help of dental educators, to provide dental students with clinical information and hands-on training in comprehensive periodontal treatment including ARESTIN® + scaling and root planing (SRP).

For Faculty
For Faculty
Faculty
Introduce students to patient selection and comprehensive periodontal disease treatment that includes ARESTIN® + SRP. Program materials for instructors include PowerPoint® lectures, classwork, laboratories, clinical exercises, and evaluations.
For Students
For Students
Students
Learn about periodontal disease, patient selection, and comprehensive treatment of periodontal disease that includes ARESTIN® + SRP. Program includes classroom lectures, lab work, and clinical experience. Program materials for students include an ARESTIN® Student Trial Kit and reading materials.

ARESTIN® is indicated as an adjunct to scaling and root planing (SRP) procedures for reduction of pocket depth in patients with adult periodontitis. ARESTIN® may be used as part of a periodontal maintenance program, which includes good oral hygiene and SRP.

IMPORTANT SAFETY INFORMATION

ARESTIN® should not be used in any patient who has a known sensitivity to minocycline or tetracyclines. The use of drugs of the tetracycline class during tooth development may cause permanent discoloration of the teeth, and therefore should not be used in children or in pregnant or nursing women. Hypersensitivity reactions that included, but were not limited to, anaphylaxis, angioneurotic edema, urticaria, rash, swelling of the face and pruritus have been reported with the use of ARESTIN®. In clinical trials, the most frequently reported nondental treatment-emergent adverse events were headache, infection, flu syndrome and pain.

Please see Full Prescribing Information

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch, or call 1-800-FDA-1088.

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