1. What is innohep and what it is used for
2. What you need to know before starting to use innohep
3. How to use innohep
4. Possible side effects
5. Storage of innohep
6. Contents of the pack and additional information l
innohepis a medication that inhibits the natural ability of blood to form clots (coagulate).
-innohep is used to treat blood clots and prevent the formation of more clots in adults.
You should consult a doctor if you get worse or do not improve.
No use Innohep
-If you are allergic to tinzaparin sodium or any of the other components of this medication (listed in section 6).
-If you have or have had heparin-induced thrombocytopenia.
-If you have a severe bleeding (for example, in the brain, spinal cord, eyes, or stomach).
-If you have a severe heart infection (septic endocarditis).
-If you have a scheduled spinal or epidural anesthesia or lumbar puncture.
Warnings and Precautions
Consult your doctor or nurse before starting to use Innohep
Children and Adolescents
Innohep is not indicated for use in children and adolescents.
Use of Innohep with Other Medications
Inform your doctor or pharmacist if you are using, have used recently, or may need to use any other medication. Some medications may interact with the effect of Innohep.
Inform your doctor if you are using any of the following medications as you may bleed more easily:
-Medications for the treatment of inflammation and pain, especially nonsteroidal anti-inflammatory drugs (NSAIDs), such as acetylsalicylic acid
-Medications used to dissolve blood clots in the blood (thrombolytic agents)
-Medications that block the action of vitamin K (vitamin K antagonists).
-Activated protein C.
-Direct inhibitors of factor Xa and IIa.
Pregnancy and Breastfeeding
If you are pregnant or breastfeeding, or think you may be pregnant, consult your doctor or pharmacist before using this medication.
Innohep in pre-filled syringes can be used during all trimesters of pregnancy.
If epidural anesthesia is necessary, inform your doctor that you are using Innohep.
Inform your doctor or nurse if you have a heart valve prosthesis
Driving and Operating Machines
Innohep does not affect the ability to drive or operate machines.
Innohep Contains Sodium Metabisulfite
-As Innohep contains sodium metabisulfite as an excipient, it may cause rare severe allergic reactions and bronchospasm.
-This medication contains 40 mg of sodium (main component of table salt/for cooking) in each ml. This is equivalent to 2% of the maximum daily sodium intake recommended for an adult.
Follow exactly the administration instructions of this medication indicated by your doctor or nurse. In case of doubt, consult your doctor or nurse again..
During treatment, your doctor may request that you undergo routine blood tests to evaluate the effect of innohep.
Innohep must be injected under the skin (subcutaneous injection). Avoid administering other medications via intramuscular injection during innohep treatment due to the risk of hematoma.
The recommended dose is:
175 UI anti-Xa per kg of body weight administered once a day.
Your doctor will indicate the suitable dose for you.
The treatment should be administered once a day for 6 days, and may be extended up to 6 months. The need to extend treatment for more than 6 months should be evaluated by your doctor. Your doctor will indicate the duration of your treatment.
Instructions on how to inject innohep:
1.Wash your hands carefully before injecting this medication. Clean the skin around the injection site with an alcohol swab and let it dry without rubbing it.
2.Open the syringe container by lifting the color-coded cap completely back and remove the syringe.
Inspect the syringe contents before use. If you observe turbidity or a precipitate in the medication, do not use it and take another syringe. The medication may exhibit a yellowish color during storage, but it can be used as long as the solution is transparent and does not exceed the expiration date. Each syringe can be used only once.
3.Push the safety device downwards, separating it from the protective cap of the needle.
4.Remove the protective cap from the needle without twisting it. Adjust the syringe contents to the prescribed dose by your doctor. Discard the excess volume by pressing the plunger in a vertical position. Do not pull the plunger back or remove the air bubble contained in the syringe. If the air bubble is not correctly positioned next to the plunger, gently tap the syringe until the air bubble is in its place.
5.Take a skin fold, without pressing, between the thumb and index finger of one hand and with the other hand,insert the needle vertically and slowly into the skin fold, that is, at a right angle to the skin.
6.Inject the necessary dose slowly into the fatty tissue, for example, the skin of the abdominal area, the anterior area of the thighs, the lower back, or the posterior area of the arms. Wait a few seconds to allow the solution to distribute before removing the needle and releasing the skin fold.
7.Clean the area with a gauze if blood has come out. Choose a different injection site for the next time (for example, alternating between the left and right abdominal areas).
8.Push the safety device back to its original position so that it is parallel to the needle. Then, with the safety device flat on a rigid surface, press down until the needle is locked in the device.
9.The used syringe, with the needle pointing downwards, can be inserted into the same syringe container or a puncture waste container. In this way, the syringe is safe, and the syringe container or puncture waste container can be delivered to a hospital or pharmacy for destruction.
If you use more innohep than you should
If you are treated with more innohep than you need, bleeding may occur. Consult your doctor or nurse immediately if you do not feel well or think you have administered too much innohep.
If you forgot to use innohep
You should not inject a double dose to compensate for the missed dose. If you have forgotten to administer more than one dose, consult your doctor as soon as possible.
If you interrupt the treatment with innohep
If you interrupt the administration of innohep, the effect of making blood thinner will cease. Do not interrupt innohep treatment without consulting your doctor or nurse.
If you have any other doubts about the use of this medication, ask your doctor or nurse.
Like all medications, innohep may cause side effects, although not everyone will experience them.
Severe side effects:
In rare cases, severe side effects have been observed that require immediate medical attention during innohep treatment. If you experience any of the following symptoms, consult your doctor immediately or go to the nearest hospital for emergency treatment.
With innohep administration, the following side effects have been observed:
Frequent: may affect up to 1 in 10 people
Rare: may affect up to 1 in 100 people
Rare: may affect up to 1 in 1,000 people
Pediatric population
There is limited information, from a clinical trial and post-marketing data, indicating that the adverse reaction profile in children and adolescents is comparable to that observed in adults.
Reporting of side effects
If you experience any type of side effect, consult your doctor, pharmacist, or nurse, even if it is a possible side effect not listed in this prospectus. You can also report them directly through theSpanish System for Pharmacovigilance of Medicinal Products for Human Use: https://www.notificaram.es. By reporting side effects, you can contribute to providing more information on the safety of this medication.
-Keep this medication out of the sight and reach of children.
No use this medication after the expiration date that appears on the packaging. The expiration date is the last day of the month indicated.
-No special storage conditions are required.
-Do not usethis medicationif you observe turbidity or a precipitate in the syringe.
-The solution may present a yellowish color during storage, but this does not affect the quality of the product, which is still safe for use.
Composition of innohep
-The active ingredient is tinzaparina sodium. Each ml of injectable solution contains 20,000 UI anti-Xa of tinzaparina sodium.
-The other components are sodium metabisulphite (E 223), sodium hydroxide and water for injections.
Appearance of the product and contents of the packaging
Injectable solution.
Glass transparent syringes containing a colourless or pale yellow solution, free from turbidity and deposit, when left to stand.
Packaging sizes:
Only some packaging sizes may be commercially available.
Holder of the marketing authorization and responsible for manufacturing
Holder of the marketing authorization:
LEO Pharma A/S
Industriparken 55,
DK-2750 Ballerup
Denmark
Responsible for manufacturing:
Laboratoires LEO S.A.
39 Route de Chartres,
FR-28500 Vernouillet Cedex
France
Date of the last review of this leaflet:December 2019.
The detailed and updated information on this medicine is available on the website of the Spanish Agency for Medicines and Medical Devices (AEMPS) http://www.aemps.gob.es/.
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