LOVENOX®- Talk to Your Doctor About DVT Blood Clot
sanofi-aventis homepage sanofi-aventis homepage  
KNOW LOVENOX®

Talking to Your Doctor

DVT blood clots may develop in people with certain medical and surgical conditions, including:

  • Certain types of cancer
  • Congestive heart failure
  • Flare-ups of chronic obstructive pulmonary disease (COPD)
  • Certain surgeries, particularly hip- or knee-replacement surgery, as well as abdominal surgery
  • Acute illness resulting in extended periods of immobility

If you are in the hospital or plan to be in the hospital, you need to proactively discuss your risk of developing DVT blood clots with the healthcare professionals who are managing your care. These include your doctors, surgeons, and nurses, who will help you determine if you are at risk of developing DVT blood clots.

During your discussions with your medical team prior to your hospital stay, you may want to use this list of Questions to Ask Your Doctor regarding DVT blood clots and treatment with LOVENOX®. It includes questions such as:

"How long can I expect to be in the hospital?"
"Are there any different medications I'll be receiving while I'm in the hospital?"
"Is LOVENOX® right for me?"

By proactively discussing your risk with your healthcare professional, you are taking the first step toward reducing your risk.

Download the full list of Questions to Ask Your Doctor   Download the full list of Questions to Ask Your Doctor (PDF)

You need the Adobe® Reader® installed on your computer to view PDF documents. You can download a copy of the Adobe® Reader® by clicking the link below.

Adobe Download Page

Adobe® and Adobe® Reader® are registered trademarks of Adobe Systems Incorporated.

LOVENOX® can help reduce the risk of developing DVT blood clots, which may lead to PE, in patients undergoing abdominal surgery, hip- or knee-replacement surgery, or in acutely ill medical patients with severely restricted mobility.

INDICATIONS

LOVENOX® is indicated for the prophylaxis of deep vein thrombosis, which may lead to pulmonary embolism:

  • in patients undergoing abdominal surgery who are at risk for thromboembolic complications;
  • in patients undergoing hip-replacement surgery, during and following hospitalization;
  • in patients undergoing knee-replacement surgery;
  • in medical patients who are at risk for thromboembolic complications due to severely restricted mobility during acute illness.

LOVENOX® injection is indicated for:

  • the inpatient treatment of acute deep vein thrombosis, with or without pulmonary embolism, when administered in conjunction with warfarin sodium;
  • the outpatient treatment of acute deep vein thrombosis, without pulmonary embolism, when administered in conjunction with warfarin sodium.
Important Safety Information

Certain procedures, called "epidural/spinal anesthesia" and "spinal puncture," may be used as a normal part of hospitalization. Patients requiring these procedures while being treated with LOVENOX® or other low-molecular-weight heparins are at risk of developing a blood clot in or around the spine. This condition may result in long-term or permanent paralysis.

LOVENOX® is not the same as "unfractionated heparin" or other drugs called "low-molecular-weight heparins." Therefore, these drugs cannot be used interchangeably with LOVENOX®.

LOVENOX® can alter the blood’s ability to clot. Patients treated with LOVENOX®, who also have conditions affecting the clotting system, must be carefully monitored by their physician. Adjusting the dose of LOVENOX® may be necessary for patients who have certain forms of kidney disease. All patients receiving LOVENOX®, as well as other anticoagulants, should be carefully monitored for bleeding by their physician. Bleeding can occur at any site with LOVENOX® use.

Platelet drops, known as "thrombocytopenia," can occur with LOVENOX® use. Cases of a related condition called "heparin-induced thrombocytopenia" have been observed in clinical practice. If you have had this condition, you must notify your healthcare professional. Your physician may perform blood tests to monitor for the occurrence of any drop in platelet count.

The use of LOVENOX® has not been adequately studied in pregnant women with artificial (mechanical) heart valves.

LOVENOX® should not be used in patients with an allergy or sensitivity reaction to the active ingredient called enoxaparin sodium, heparin, or pork products, and in patients with active major bleeding.

Common side effects include mild local reactions or irritation at the site of injection, pain, bruising, and redness of skin.

For specific questions about your health, you should always consult your physician or a qualified healthcare professional who is responsible for your care.

Please see Full Prescribing Information including boxed WARNING for additional important information.