Before using abarelix, tell your doctor if you
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have irregular heartbeats;
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have liver problems;
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have osteoporosis; or
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weigh more than 225 pounds.
You may not be able to use abarelix, or you may require a dosage adjustment or special monitoring during treatment.
Abarelix is not intended for use by women. Abarelix is in the FDA pregnancy category X. This means that abarelix will cause birth defects in an unborn baby. Do not use this medication if you are pregnant or if you could become pregnant during treatment.
Abarelix is not intended for use by women. It is not known whether abarelix passes into
breast milk.
Abarelix must be administered by a qualified healthcare provider.
Abarelix is administered as an injection into the muscle.
In some cases, the use of abarelix has resulted in serious allergic reactions. An allergic reaction may occur after any injection of the medication, including, but not limited to the first dose. Patients should be observed in the doctor’s office for at least 30 minutes following each dose so that immediate treatment of an allergic reaction can be obtained if needed.
Treatment with abarelix may become less effective over time in some patients. Monitoring blood levels of testosterone will be done on a regular basis with blood tests to monitor the effectiveness of the medication.
It is important to use abarelix regularly to get the most benefit.
Abarelix vials for injection should be stored at room temperature away from moisture and heat.
Contact your doctor if you miss a dose of abarelix.
In some cases, the use of abarelix has resulted in serious allergic reactions. An allergic reaction may occur after any injection of the medication, including, but not limited to the first dose. Patients should be observed in the doctor’s office for at least 30 minutes following each dose so that immediate treatment of an allergic reaction can be obtained if needed.
Other, less serious side effects may be more likely to occur. Talk to your doctor if you experience
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hot flashes;
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sleep disturbances;
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breast enlargement or pain;
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diarrhea or constipation;
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swelling;
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nausea;
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dizziness;
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headache;
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fatigue; or
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changes with or difficulty urinating.
Side effects other than those listed here may also occur. Talk to your doctor about any side effect that seems unusual or that is especially bothersome.
In some cases, the use of abarelix has resulted in serious allergic reactions. An allergic reaction may occur after any injection of the medication, including, but not limited to the first dose. Patients should be observed in the doctor’s office for at least 30 minutes following each dose so that immediate treatment of an allergic reaction can be obtained if needed.
Treatment with abarelix may become less effective over time in some patients. Monitoring blood levels of testosterone will be done on a regular basis with blood tests to monitor the effectiveness of the medication.
Abarelix is not intended for use by women. Abarelix is in the FDA pregnancy category X. This means that abarelix will cause birth defects in an unborn baby. Do not use this medication if you are pregnant or if you could become pregnant during treatment.
There are no restrictions on food, beverages, or activities while using abarelix. Follow any special instructions given by your doctor.
It is not known whether abarelix will interact with other medicines. Talk to your doctor and pharmacist before taking any prescription or over-the-counter medicines, including herbal products during treatment with abarelix.
An overdose of abarelix is unlikely to occur. If you do suspect that an overdose has occurred, contact your doctor, hospital emergency room, or poison control center for advice.