Patient leaflet - TAKHZYRO 300 MG SOLUTION FOR INJECTION
1. what takhzyro is and what it is used for
TAKHZYRO contains the active substance lanadelumab.
What TAKHZYRO is used for
TAKHZYRO is a medicine used in adults, and adolescents aged 12 years and older to prevent angioedema attacks, in patients with HAE.
What hereditary angioedema (HAE) is
- HAE is a condition which runs in families. With this condition your blood does not have enough of a protein called ‘C1 inhibitor’, or C1 inhibitor does not work properly. This leads to too much ‘plasma kallikrein’, which in turn produces higher levels of ‘bradykinin’ in your bloodstream. Too much bradykinin leads to symptoms of HAE like swelling and pain on the, hands and feet
- face, eyelids, lips or tongue
- voice-box (larynx), which may make breathing difficult
- genitals
How TAKHZYRO works
TAKHZYRO is a type of protein that blocks the activity of plasma kallikrein. This helps to reduce the amount of bradykinin in your bloodstream and prevents symptoms of HAE.
2. what you need to know before you use takhzyrodo not use takhzyro:if you are allergic to lanadelumab or any of the other ingredients of this medicine (listed in section 6).
Warnings and precautions
- Talk to your doctor, pharmacist or nurse before using TAKHZYRO.
- If you have a severe allergic reaction to TAKHZYRO with symptoms such as a rash, a tight chest, wheezing, or a fast heartbeat, tell your doctor, pharmacist or nurse immediately.
Keeping a record
It is strongly recommended that every time you have a dose of TAKHZYRO, you write down the name and batch number of the medicine. This is so that you keep a record of the batches used.
Laboratory tests
Tell your doctor if you are using TAKHZYRO before you have laboratory tests to measure how well your blood is clotting. This is because TAKHZYRO in the blood may interfere with some laboratory tests, leading to inaccurate results
Children and adolescents
TAKHZYRO is not recommended for use in children under 12 years of age. This is because it has not been studied in this age group.
Other medicines and TAKHZYRO
Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines.
TAKHZYRO is not known to affect other medicines or be affected by other medicines.
Pregnancy and breast-feeding
If you are pregnant or breast-feeding, think you may be pregnant or are planning to have a baby, ask your doctor or pharmacist for advice before starting to use Takhzryo. There is limited information on the safety of TAKHZYRO use during pregnancy and breast-feeding. As a precautionary measure, it is preferable to avoid the use of lanadelumab during pregnancy and breast-feeding. Your doctor will discuss with you the risks and benefits of taking this medicine.
Driving and using machines
This medicine has negligible influence on the ability to drive or use machines.
TAKHZYRO contains sodium
The medicine contains less than 1 mmol sodium (23 mg) per ml of solution, that is to say essentially ‘sodium-free’.
3. how to use takhzyro
TAKHZYRO is provided in single-use vials as ready-to-use solution. Your treatment will be started and managed under the supervision of a doctor experienced in the care of patients with HAE.
Always use this medicine exactly as described in this leaflet or as your doctor, pharmacist or nurse has told you. Check with your doctor, pharmacist or nurse if you are not sure or have any further questions on the use of this medicine.
How much TAKHZYRO to use
The recommended starting dose is 300 mg every 2 weeks. If you have not had an attack for a long period, your doctor may change the dose to 300 mg every 4 weeks, especially if you have a low body weight.
How to inject TAKHZYRO
If you inject TAKHZYRO yourself or if your caregiver injects it, you or your caregiver must carefully read and follow the instructions in section 7, “Instructions for use”.
- TAKHZYRO is for injection under the skin (‘subcutaneous injection’).
- The injection can be given either by yourself or a caregiver.
- A doctor, pharmacist or nurse should show you how to prepare and inject TAKHZYRO properly before you use it for the first time. Do not inject yourself or someone else until you have been trained to inject the medicine.
- Insert the needle into the fatty tissue in the tummy (abdomen), thigh or upper arm.
- Inject the medicine in a different place each time.
- Use each vial of TAKHZYRO only once.
If you use more TAKHZYRO than you should
Tell your doctor, pharmacist or nurse if you take too much TAKHZYRO.
If you forget to use TAKHZYRO
If you miss a dose of TAKHZYRO, inject your dose as soon as possible but there must be at least 10 days between each dose. If you are not sure when to inject TAKHZYRO after a missed dose, ask your doctor, pharmacist or nurse.
If you stop using TAKHZYRO
It is important that you keep injecting TAKHZYRO as instructed by your doctor even if you feel better.
If you have any further questions on the use of this medicine, ask your doctor, pharmacist or nurse.
4. possible side effects
Like all medicines, this medicine can cause side effects, although not everybody gets them.
If you have a severe allergic reaction to TAKHZYRO with symptoms such as a rash, tight chest, wheezing, or a fast heart beat, tell your doctor, pharmacist or nurse immediately.
Tell your doctor, pharmacist or nurse if you notice any of the following side effects.
Very common (may affect more than 1 in 10 people):
- Reactions where the injection is given – symptoms include pain, skin redness, bruising, discomfort, swelling, bleeding, itching, hardening of skin, tingling, warmth and rash.
- Allergic reactions including itching, discomfort and tingling of the tongue
- Dizziness, feeling faint
- Raised skin rash
- Muscle pain
- Blood tests showing liver changes
Reporting of side effects
If you get any side effects, talk to your doctor, pharmacist or nurse. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via
United Kingdom
Yellow Card Scheme
Website: or search for MHRA Yellow Card in the Google Play or
Apple App Store
By reporting side effects you can help provide more information on the safety of this medicine.
5. how to store takhzyro
Keep this medicine out of the sight and reach of children.
Do not use this medicine after the expiry date which is stated on the label after EXP. The expiry date refers to the last day of that month.
Store in a refrigerator (2°C-8°C). Do not freeze. Keep the vial in the outer carton in order to protect from light.
Vials may be stored below 25°C for a single period of 14 days, but not beyond the expiry date.
Do not return TAKHZYRO to refrigerated storage after storage at room temperature.
Do not use this medicine if you notice signs of deterioration such as particles in the vial or changed colour of the injection solution.
Do not throw away any medicines via wastewater or household waste. Ask your pharmacist how to throw away medicines you no longer use. These measures will help protect the environment.
6. contents of the pack and other informationwhat takhzyro contains the active substance is lanadelumab. each vial contains 300 mg of lanadelumab in 2ml solution.
- The other ingredients are disodium phosphate dihydrate, citric acid monohydrate, histidine, sodium
chloride, polysorbate 80 and water for injections – see section 2 “TAKHZYRO contains sodium”’
What TAKHZYRO looks like and contents of the pack
TAKHZYRO is presented as a clear, colourless to slightly yellow solution for injection in a glass vial.
TAKHZYRO is available as a single pack containing one 2 ml vial and in multipacks comprising 2 or 6 cartons, each carton containing 1 vial.
Not all pack sizes may be marketed.
Each pack also contains the following items:
- Empty 3 ml syringe
- 18 gauge blunt tip vial access needle
- 27 gauge x 13 mm pointed tip administration (injection) needle.
Marketing Authorisation Holder
Takeda Pharmaceuticals International AG Ireland Branch
Block 3 Miesian Plaza
50–58 Baggot Street Lower
Dublin 2
Ireland
Tel: +80066838470
E-mail:
Manufacturer
Shire Pharmaceuticals Ireland Limited
Blocks 2 & 3 Miesian Plaza
50–58 Baggot Street Lower
Dublin 2
Ireland
Tel: +80066838470
E-mail:
This leaflet was last revised in 10/2021.
7. instructions for use
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e) Push the plunger slowly until all the medicine has been injected. Release the skin fold and gently remove the needle. Do not recap the needle.
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f) Place the 27 gauge x 13 mmpointed-tip injection needle and the syringe in a sharps container.