Do not use FILOKYP:
- If you are hypersensitive (allergic) to carfilzomib or any of the other ingredients of this medicine (listed in section 6).
- If you are pregnant or breastfeeding.
Tell your doctor or healthcare professional before being given the injection if:
- You have heart problems, including a history of chest pain (angina pectoris), heart attack, irregular heartbeat, high blood pressure or if you have ever taken a medicine for your heart.
- You have lung problems, including a history of shortness of breath at rest or with activity (dyspnoea).
- You have kidney problems, including kidney failure or if you have ever received dialysis.
- You have liver problems, including a history of hepatitis, fatty liver, or if you have ever been told your liver is not working properly.
- You have unusual bleeding, including easy bruising, bleeding from an injury, such as a cut that does not stop bleeding in a normal amount of time, or internal bleeding which can indicate you have low platelets.
- You have blood clots in your veins or lungs.
- You have any other major medical disease for which you were hospitalised or received medication.
You may need extra tests to check that your heart, kidneys and liver are working properly.
Using other medicines with FILOKYP:
Always tell your healthcare professional the name of all the medications you are currently taking, have recently taken, or might take in the future. This includes any medicines obtained without a prescription, such as vitamins or herbal remedies (This includes complementary or traditional medicines).
Tell your doctor or nurse if you are taking medicines used to prevent pregnancy such as oral contraceptives or other hormonal contraceptives since these may not be suitable for use with FILOKYP.
Pregnancy, breastfeeding and fertility:
For women receiving FILOKYP If you are pregnant or breastfeeding, think you may be pregnant or are planning to have a baby, please consult your doctor, pharmacist or other health care provider for advice before taking this medicine. FILOKYP should not be used if you are trying to become pregnant or are pregnant. Treatment with FILOKYP has not been evaluated in pregnant women. While receiving FILOKYP and for 30 days after stopping treatment, you should use a reliable method of birth control to ensure you do not become pregnant. You should talk to your doctor or nurse about reliable methods of birth control. It is important that you tell your doctor if you are pregnant, think you may be pregnant, or plan on becoming pregnant. If you become pregnant while receiving FILOKYP, notify your doctor immediately. If you are breastfeeding, you should not receive FILOKYP. It is not known if FILOKYP passes into breast milk in humans. It is important to tell your healthcare professional if you are breastfeeding or plan to do so.
For men receiving FILOKYP While receiving FILOKYP and for 90 days after stopping treatment, you should use a reliable method of birth control, such as a condom, to ensure your partner does not become pregnant. You should talk to your doctor or nurse about reliable methods of birth control. If your partner becomes pregnant while you are receiving FILOKYP or within 90 days after stopping treatment, notify your doctor or nurse immediately.
Driving and using machinery:
Patients being treated with FILOKYP may experience fatigue, dizziness, fainting, and/or a drop in blood pressure. This may impair your ability to drive or operate machinery. If you have these symptoms; you should not drive a car or operate machinery. It is not always possible to predict to what extent FILOKYP may interfere with the daily activities of a patient. Patients should ensure that they do not engage in the above activities until they are aware of the measure to which FILOKYP affects them.
FILOKYP contains sodium:
The medicine contains 216 mg sodium (main component of cooking/table salt) in 60 ml vial this is equivalent to 11 % of the WHO recommended maximum daily intake of 2 g sodium for an adult.
FILOKYP contains cyclodextrin:
This medicine contains 3,000 mg cyclodextrin (betadex sulfobutyl ether sodium) per 60 mg vial. This is equivalent to 88 mg/kg for a 70 kg adult.