Managing Side Effects With LUPRON DEPOT

Managing side effects

Some side effects are common when taking hormone therapy like LUPRON DEPOT. It’s important to understand potential side effects and be prepared to manage those that are bothersome.

Photo of 2 men playing one-on-one basketball on an outdoor court.

Always report side effects to your doctor

Your doctor is the best equipped to evaluate your side effects and recommend ways to manage them. The information here is not intended to replace the advice of your doctor.

Hot flashes

Hot flashes are the most common side effect of hormone therapies like LUPRON DEPOT. They feel like a sudden rush of warmth in the upper body, usually the face, neck, and chest. You may want to cool yourself down while experiencing a hot flash, but if you lose too much body heat, you may feel cold afterward.

Fatigue or weakness

Getting enough sleep, eating healthy foods, and exercising can help reduce your fatigue. Fatigue can be caused by other health conditions not related to your treatment, so it’s important to report any fatigue to your doctor.

Injection site reactions or pain

You may experience some soreness, redness, or itchiness after each injection, which may last a day or more. Talk to your doctor about ways to manage this possible side effect.

“I exercise every morning because I find that it helps. After my workout, I’m ready to face the day.”

Freeze-frame image from Larry’s video as he discusses his exercise routine.

Individual results may vary.

“I exercise every morning because I find that it helps. After my workout, I’m ready to face the day.”

– Larry, LUPRON DEPOT advanced prostate cancer patient

– Larry, LUPRON DEPOT advanced prostate cancer patient.

SEE LARRY’S STORY

Individual results may vary.

USE

LUPRON DEPOT^®(leuprolide acetate for depot suspension) 7.5 mg for 1-month, 22.5 mg for 3-month, 30 mg for 4-month, and 45 mg for 6-month administration are prescribed for the treatment of advanced prostate cancer.
LUPRON DEPOT is a prescription medication that must be administered in your doctor’s office.

Important Safety Information

LUPRON DEPOT is not for people who have had any type of allergic reaction to LUPRON DEPOT or similar drugs.
LUPRON DEPOT causes an increase in testosterone during the first few weeks of therapy.
- Some men may experience temporary new or worsening symptoms of prostate cancer, including urinary symptoms and/or bone pain.
- If your cancer has spread to the spine or urinary tract, urinary blockage or pressure on the spine may occur and can sometimes lead to paralysis, which may be life-threatening.
- You may require close medical attention during the first few weeks of therapy. Notify your doctor if you develop any new or worsened symptoms after beginning LUPRON DEPOT treatment.
High blood sugar and increased risk of diabetes can occur in men using LUPRON DEPOT. Your doctor will monitor your blood sugar during treatment.
Increased risk of heart attack, sudden death, and stroke can occur in men using LUPRON DEPOT. Discuss this increased risk with your doctor before starting treatment and report any new symptoms during treatment.
LUPRON DEPOT can affect the electrical activity of your heart. Your doctor must determine if the benefits of using LUPRON DEPOT outweigh the risks, especially if you have congenital long QT syndrome, abnormal blood tests for electrolytes, congestive heart failure, or if you take medications to regulate your heartbeat.
Convulsions have been observed in patients taking leuprolide acetate, including patients who have a history of seizures, epilepsy, or brain disorders (related to blood vessels, nerves, or tumors), and in those taking medications associated with convulsions. Convulsions have also been reported in patients without any of these conditions.
Regular blood tests are needed to check your testosterone and prostate-specific antigen (PSA) levels.
LUPRON DEPOT may cause fetal harm if administered to a pregnant woman.
LUPRON DEPOT may cause impotence.
The most common side effects of LUPRON DEPOT include hot flashes/sweats; injection site reaction/pain; general pain; swelling; testicular shrinkage; difficulty urinating; fatigue/weakness; headache; and joint, gastrointestinal, and respiratory problems.

For more information, talk with your healthcare provider.

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.

If you are having difficulty paying for your medicine, AbbVie may be able to help. Visit AbbVie.com/myAbbVieAssist to learn more.

US-LUPR-220200

Please click here for Full Prescribing information.

USE

LUPRON DEPOT^® (leuprolide acetate for depot suspension) 7.5 mg for 1-month, 22.5 mg for 3-month, 30 mg for 4-month, and 45 mg for 6-month administration are prescribed for the treatment of advanced prostate cancer. LUPRON DEPOT is a prescription medication that must be administered in your doctor’s office.

Important Safety Information

LUPRON DEPOT is not for people who have had any type of allergic reaction to LUPRON DEPOT or similar drugs. LUPRON DEPOT causes an increase in testosterone during the first few weeks of therapy.Some men may experience temporary new or worsening symptoms of prostate cancer, including urinary symptoms and/or bone pain.

Important Safety Information

LUPRON DEPOT is not for people who have had any type of allergic reaction to LUPRON DEPOT or similar drugs. LUPRON DEPOT causes an increase in testosterone during the first few weeks of therapy.Some men may experience temporary new or worsening symptoms of prostate cancer, including urinary symptoms and/or bone pain.

Important Safety Information

LUPRON DEPOT is not for people who have had any type of allergic reaction to LUPRON DEPOT or similar drugs. LUPRON DEPOT causes an increase in testosterone during the first few weeks of therapy.Some men may experience temporary new or worsening symptoms of prostate cancer, including urinary symptoms and/or bone pain.

USE

LUPRON DEPOT^® (leuprolide acetate for depot suspension) 7.5 mg for 1-month, 22.5 mg for 3-month, 30 mg for 4-month, and 45 mg for 6-month administration are prescribed for the treatment of advanced prostate cancer. LUPRON DEPOT is a prescription medication that must be administered in your doctor’s office.

Important Safety Information

LUPRON DEPOT is not for people who have had any type of allergic reaction to LUPRON DEPOT or similar drugs. LUPRON DEPOT causes an increase in testosterone during the first few weeks of therapy.Some men may experience temporary new or worsening symptoms of prostate cancer, including urinary symptoms and/or bone pain.

USE

LUPRON DEPOT^® (leuprolide acetate for depot suspension) 7.5 mg for 1-month, 22.5 mg for 3-month, 30 mg for 4-month, and 45 mg for 6-month administration are prescribed for the treatment of advanced prostate cancer. LUPRON DEPOT is a prescription medication that must be administered in your doctor’s office.

Important Safety Information

LUPRON DEPOT is not for people who have had any type of allergic reaction to LUPRON DEPOT or similar drugs. LUPRON DEPOT causes an increase in testosterone during the first few weeks of therapy.Some men may experience temporary new or worsening symptoms of prostate cancer, including urinary symptoms and/or bone pain.

USE

LUPRON DEPOT^®(leuprolide acetate for depot suspension) 7.5 mg for 1-month, 22.5 mg for 3-month, 30 mg for 4-month, and 45 mg for 6-month administration are prescribed for the treatment of advanced prostate cancer.
LUPRON DEPOT is a prescription medication that must be administered in your doctor’s office.

Important Safety Information

LUPRON DEPOT is not for people who have had any type of allergic reaction to LUPRON DEPOT or similar drugs.
LUPRON DEPOT causes an increase in testosterone during the first few weeks of therapy.
- Some men may experience temporary new or worsening symptoms of prostate cancer, including urinary symptoms and/or bone pain.
- If your cancer has spread to the spine or urinary tract, urinary blockage or pressure on the spine may occur and can sometimes lead to paralysis, which may be life-threatening.
- You may require close medical attention during the first few weeks of therapy. Notify your doctor if you develop any new or worsened symptoms after beginning LUPRON DEPOT treatment.
High blood sugar and increased risk of diabetes can occur in men using LUPRON DEPOT. Your doctor will monitor your blood sugar during treatment.
Increased risk of heart attack, sudden death, and stroke can occur in men using LUPRON DEPOT. Discuss this increased risk with your doctor before starting treatment and report any new symptoms during treatment.
LUPRON DEPOT can affect the electrical activity of your heart. Your doctor must determine if the benefits of using LUPRON DEPOT outweigh the risks, especially if you have congenital long QT syndrome, abnormal blood tests for electrolytes, congestive heart failure, or if you take medications to regulate your heartbeat.
Convulsions have been observed in patients taking leuprolide acetate, including patients who have a history of seizures, epilepsy, or brain disorders (related to blood vessels, nerves, or tumors), and in those taking medications associated with convulsions. Convulsions have also been reported in patients without any of these conditions.
Regular blood tests are needed to check your testosterone and prostate-specific antigen (PSA) levels.
LUPRON DEPOT may cause fetal harm if administered to a pregnant woman.
LUPRON DEPOT may cause impotence.
The most common side effects of LUPRON DEPOT include hot flashes/sweats; injection site reaction/pain; general pain; swelling; testicular shrinkage; difficulty urinating; fatigue/weakness; headache; and joint, gastrointestinal, and respiratory problems.

For more information, talk with your healthcare provider.

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.

If you are having difficulty paying for your medicine, AbbVie may be able to help. Visit AbbVie.com/myAbbVieAssist to learn more.

US-LUPR-220200