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TESTOPEL® TREATMENT
FOR LOW TESTOSTERONE IN ADULT MALES
Testopel®
is indicated for the treatment of conditions associated with low or absent
testosterone in adult males. This
condition is also referred to as Low Testosterone (Low T) or Testosterone
Deficiency Syndrome. Testopel® is
unique. It is the only FDA-approved
implantable testosterone pellet. Placed
every 3 to 6 months in your doctor’s office, Testopel® is the only testosterone
replacement therapy that normalizes testosterone levels for 3-6 months per
dose. Other testosterone therapies may
require frequent injections into the muscle or daily topical application. If
you have been diagnosed with testosterone deficiency, speak with your physician
about your treatment options to determine if Testopel is right for you.
Commonly Asked Questions About
Testopel®:
Q: What is the
size of a Testopel® pellet?
A: Each cylindrical
Testopel pellet is small, about 4 mm long (about half the width of a dime) and
about
the diameter of a ball point pen refill.
Q: Where is
Testopel® inserted?
A: It is placed
just under the skin in the hip area.
Q: How is the
pellet inserted?
A: The insertion
will take place in the doctor’s office and only takes 5-10 minutes. Local anesthesia
(Lidocaine) will numb the area. A Band-Aid will cover the insertion
site.
Q: How will my
doctor know when to replace my Testopel®?
A: Your doctor
may either schedule a follow-up visit or if you feel your symptoms returning,
you
should contact your doctor so your
testosterone levels can be measured.
Generally, it will last 3-4
months.
Q: Are there any
complications to the insertion?
A: You may have
some discomfort for a few days. There
may be some bruising, too. Infections
are
very rare but can be treated with
antibiotics.
Q: When can I
resume sexual activity?
A: Immediately.
Q: What can I
expect after my Testopel® replacement?
A: You can
return to work immediately. It is
advisable not to swim, use a hot tub or lift heavy weights
for a few days after Testopel® is placed,
but you may otherwise resume normal
activity. You
may
experience soreness and/or bruising at the insertion site. Please follow your doctor’s
instructions.
Q: Are there
patients who should not receive Testopel® treatment?
A: Yes. You should not receive any testosterone
replacement therapy if you have ever had prostate
or breast cancer. You should not use it if you have experienced
an allergic reaction to it. Please
see the warnings and contraindications
sections of the complete prescribing information.
Q: Will my
insurance pay for Testopel®?
A: The majority
of insurance plans will cover Testopel®.
It can be treated as either a medical or
pharmacy benefit depending on your
plan. You would need to contact your
insurance company to
verify if treatment is covered on your
policy.
Contact
your doctor for complete information, risks and benefits regarding Testopel
treatment®. You can also go to www.testopel.com.