Let's take a minute to talk about your medication. 

This is Monoclate-P. This medicine contains a blood clotting factor called 'Factor VIII'. People with hemophilia A do not have enough Factor VIII, and they are at risk for bleeding. Monoclate-P raises the levels of Factor VIII in the blood, which can prevent and control bleeding. 

Monoclate-P is given into a vein. This is known as an 'intravenous' or 'IV' infusion. You may receive your doses in a clinic, at your doctor's office, or at home. Before using this medicine at home, though, you must receive full training from your healthcare provider and read the "Instructions for Use". 

Common side effects include having mild chills or nausea. Sometimes, the injection site may sting a little. You should call your doctor if these effects or others do not go away, or if they get worse instead of better. 

As with any medicine, more serious side effects can occur. With Monoclate-P, these can include an allergic reaction. You should stop the dose and get medical help right away if you have a rash, hives, itching, wheezing, or tightness in the chest. Also, stop and get help right away for dizziness, tingling or swelling in your throat, or any other unusual changes to your body.

Because Monoclate-P is made with human blood, there is risk that it could transmit a disease, like a viral infection. Talk to your doctor or pharmacist for more information.

It is important to know that your body may form inhibitors to Factor VIII. Inhibitors can prevent Monoclate-P from working. So, call your doctor right away if your bleeding is not controlled after using this medicine. 

For best results with Monoclate-P, plan ahead for refills, and talk to your healthcare team before you travel.