ROPIVACAINE KABI 7.5 mg/mL INJECTABLE SOLUTION
How to use ROPIVACAINE KABI 7.5 mg/mL INJECTABLE SOLUTION
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This page provides general information and does not replace a doctor’s consultation. Always consult a doctor before taking any medication. Seek urgent medical care if symptoms are severe.
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Introduction
Package Leaflet: Information for the User
Ropivacaína Kabi 7.5 mg/ml injectable solution EFG
Ropivacaína, hydrochloride
Read all of this leaflet carefully before you are given this medicine because it contains important information for you.
- Keep this leaflet, you may need to read it again.
- If you have any further questions, ask your doctor, nurse or pharmacist.
- If you experience any side effects, talk to your doctor, nurse or pharmacist, even if they are not listed in this leaflet. See section 4.
The name of this medicine is “Ropivacaína Kabi 7.5 mg/ml injectable solution EFG”, but in the rest of this leaflet it will be referred to as “Ropivacaína Kabi”.
Contents of the pack:
- What Ropivacaína Kabi is and what it is used for
- What you need to know before you are given Ropivacaína Kabi
- How to use Ropivacaína Kabi
- Possible side effects
- Storage of Ropivacaína Kabi
- Contents of the pack and other information
1. What Ropivacaína Kabi is and what it is used for
- Ropivacaína Kabi contains ropivacaína hydrochloride
- It belongs to a group of medicines called local anesthetics
Ropivacaína Kabi 7.5 mg/ml injectable solution is indicated for adults and adolescents over 12 years to numb (anesthetize) specific parts of the body. It is used to stop pain or provide pain relief. It can be used for:
- Numbing parts of the body during surgery, including cesarean sections
Relieving pain during childbirth, after surgery, or after an accident
2. What you need to know before you are given Ropivacaína Kabi
Ropivacaína Kabi will not be given to you
- if you are allergic (hypersensitive) to ropivacaína hydrochlorideor to any of the other ingredients of this medicine (listed in section 6)
- if you are allergic to any other local anesthetic of the same class (such as lidocaine or bupivacaine)
- if you have been told you have low blood volume(hypovolemia)
- directly into the bloodstreamto numb a specific area of your body
- or in the neck of the uterusto relieve pain during childbirth
If you are not sure if any of the above applies to you, talk to your doctor before you are given Ropivacaína Kabi.
Warnings and precautions
Special care should be taken to avoid any injectionof Ropivacaína Kabi directly into the bloodstreamto prevent any immediate toxic effects. It should not be injected into inflamed areas.
Tell your doctor, nurse or other healthcare professional before you are given Ropivacaína Kabi:
- if your state of health is not gooddue to age or other factors
- if you have heart problems(complete or partial blockage of heart conduction)
- if you have advanced liver disease
- if you have severe kidney problems
Tell your doctor if you have any of these problems, as it may be necessary to adjust the dose of Ropivacaína Kabi.
Tell your doctor, nurse or other healthcare professional before you are given Ropivacaína Kabi:
- if you have acute porphyria(problems with the production of red blood cell pigment, which can sometimes cause neurological symptoms)
Tell your doctor if you or a family member has porphyria, as it may be necessary to use another anesthetic.
Tell your doctor about any illness or medical condition you have before starting treatment.
Children
Special care should be taken:
- In newborns, as they are more susceptible to Ropivacaína Kabi 2 mg/ml solution for infusion
- In children under 12 years, as some injections of Ropivacaína Kabi 2 mg/ml solution for infusion have not been established to numb parts of the body
Using Ropivacaína Kabi with other medicines
Tell your doctor or healthcare professional that you are using, have recently used, or may need to use any other medicine. This is because Ropivacaína Kabi can affect how some medicines work, and other medicines can affect Ropivacaína Kabi.
In particular, tell your doctor if you are using any of the following medicines:
- Other local anesthetics
- Potent pain-relieving medicines, such as morphine or codeine
- Medicines used to treat irregular heartbeats(arrhythmias), such as lidocaine or mexiletine
Your doctor needs to know this to calculate the correct dose of Ropivacaína Kabi to give you.
Also, tell your doctor if you are using any of the following medicines:
- Medicines for depression (such as fluvoxamine)
- Antibiotics to treat bacterial infections (such as enoxacin)
This is because your body takes longer to eliminate Ropivacaína Kabi if you are using these medicines. If you are using any of these medicines, prolonged use of Ropivacaína Kabi should be avoided.
Pregnancy and breastfeeding
If you are pregnant or breastfeeding, think you may be pregnant, or plan to become pregnant, talk to your doctor before you are given this medicine.
It is not known if ropivacaína affects pregnancy or if it passes into breast milk.
Ask your doctor or pharmacist for advice before taking any medicine.
Driving and using machines
Ropivacaína Kabi can cause drowsiness and affect your reaction speed. Do not drive or use tools or machines after taking Ropivacaína Kabi, until the next day.
Ropivacaína Kabi contains sodium chloride
This medicine contains 2.99 mg of sodium (a major component of table salt/cooking salt) per milliliter. This is equivalent to 0.15% of the maximum recommended daily sodium intake for an adult.
3. How to use Ropivacaína Kabi
Ropivacaína Kabi will be given to you by a doctor. The dose your doctor gives you will depend on the type of pain relief you need. It will also depend on your size, age, and physical condition.
Ropivacaína Kabi will be given to you as an injection. The part of the body where it will be used will depend on why you are being given Ropivacaína Kabi. Your doctor will give you Ropivacaína Kabi in one of the following places:
- The part of the body that needs to be numbed
- Near the part of the body that needs to be numbed
- In an area away from the part of the body that needs to be numbed. This is the case if you are given an epidural infusion (in the area near the spine)
When Ropivacaína Kabi is used in one of these ways, it prevents nerves from sending pain messages to the brain. It prevents you from feeling pain, heat, or cold where it is used, however, you may still have other sensations such as pressure or touch.
Your doctor knows the correct way to give you this medicine.
Dosage
The dose used will depend on why you are being given the medicine and your health, age, and weight.
Duration of treatment
The administration of ropivacaína usually lasts between 2 and 10 hoursin the case of anesthesiaprior to certain surgical operations and up to 72 hoursin the case of pain reliefduring and after surgery.
If you are given more Ropivacaína Kabi than you should
Severe side effects due to the administration of more Ropivacaína Kabi than necessary require special treatment, and the doctor treating you is prepared to handle these situations.
The first signs that you have been given too much Ropivacaína Kabi are usually the following:
- Ear and vision problems (vision)
- Numbness of lips, tongue, and around the mouth
- Dizziness or lightheadedness
- Tingling
- Speech disorders characterized by poor articulation (dysarthria)
- Muscle stiffness, muscle spasms, convulsions
- Low blood pressure
- Slow or irregular heartbeat
These symptoms can precede cardiac arrest, respiratory arrest, or severe convulsions.
To reduce the risk of severe side effects, your doctor will stop the administration of Ropivacaína Kabi as soon as these signs appear. This means that if any of these signs occur to you, or if you think you may have received too much Ropivacaína Kabi, tell your doctor or healthcare professional immediately.
More severe side effects from being given too much Ropivacaína Kabi include problems with speech, muscle stiffness, tremors, agitation, seizures, and loss of consciousness.
Tell your doctor or healthcare professional if you notice any of the above symptoms.
4. Possible side effects
Like all medicines, this medicine can cause side effects, although not everybody gets them.
Important side effects to look out for:
Sudden allergic reactionsthat can be life-threatening(such as anaphylaxis, including anaphylactic shock) are rare, affecting between 1 and 10 patients in every 10,000. Possible symptoms include:
- Sudden appearance of rash,
- Itching or irritation (urticaria),
- Swelling of the face, lips, tongue, or other parts of the body,
- Shortness of breath, difficulty breathing,
- Feeling of loss of consciousness.
If you think you are having an allergic reaction to Ropivacaína Kabi, tell your doctor or healthcare professional immediately.
Other possible side effects:
Very common(may affect more than 1 in 10 people)
- Low blood pressure (hypotension). This can make you feel dizzy or lightheaded
- Nausea
Common(may affect up to 1 in 10 people)
- Tingling (paresthesia)
- Dizziness
- Headache
- Slow or fast heartbeat (bradycardia, tachycardia)
- High blood pressure (hypertension)
- Vomiting
- Difficulty urinating (urinary retention)
- High temperature (fever), shivering (chills)
- Muscle stiffness (rigor)
- Back pain
Uncommon(may affect up to 1 in 100 people)
- Anxiety
- Decreased skin sensitivity
- Fainting
- Breathing difficulties
- Low body temperature (hypothermia)
- Some symptoms may occur if the injection is given into a blood vessel by mistake, or if you have been given too much Ropivacaína Kabi (see also section 3 “If you are given more Ropivacaína Kabi than you should” above). This includes seizures, dizziness or lightheadedness, numbness of the lips and around the mouth, tongue numbness, hearing problems, vision problems, speech problems, muscle stiffness, and tremors
Rare(may affect up to 1 in 1,000 people)
- Heart attack (cardiac arrest)
- Irregular heartbeat (cardiac arrhythmias)
Frequency not known(cannot be estimated from the available data):
- Horner's syndrome
Other possible side effects include:
- Numbness, due to nerve irritation caused by the needle or injection. This usually does not last long
- Involuntary muscle movements (dyskinesia)
Possible side effects detected with other local anesthetics that may also be caused by Ropivacaína Kabi include:
- Nerve damage. Rarely (affecting between 1 and 10 patients in every 10,000), this can cause permanent problems
- If Ropivacaína Kabi is given into the spinal fluid, the whole body may become numb (anesthetized)
- Receiving an epidural injection (injection into the space around the spinal nerves) can cause an interruption of a nerve pathway from the brain to the head and neck, especially in pregnant women, which can sometimes cause a condition called Horner's syndrome. This is characterized by a decrease in pupil size, drooping of the upper eyelid, and lack of sweat production from the sweat glands. It will resolve on its own when treatment is stopped
Children
In children, the side effects are the same as in adults, except for low blood pressure, which occurs less frequently in children (affecting between 1 and 10 children in every 100) and general discomfort, which occurs more frequently in children (affecting more than 1 in 10).
Reporting of side effects:
If you experience any side effects, talk to your doctor, nurse, or pharmacist, even if they are not listed in this leaflet. You can also report side effects directly through the Spanish Medicines Monitoring System for Human Use: https://www.notificaram.es. By reporting side effects, you can help provide more information on the safety of this medicine.
5. Storage of Ropivacaína Kabi
This medicine does not require special storage conditions.
Keep out of sight and reach of children.
Do not use this medicine after the expiry date stated on the blister, ampoule, or carton. The expiry date is the last day of the month stated.
Do not use this medicine if you notice a precipitate in the injectable solution.
Normally, your doctor or hospital will store Ropivacaína Kabi and are responsible for the quality of the product once opened if it is not used immediately. They are also responsible for disposing of any unused Ropivacaína Kabi correctly.
Medicines should not be disposed of via wastewater or household waste. If you are unsure, ask your pharmacist how to dispose of medicines that are no longer needed. This will help protect the environment.
6. Container contents and additional information
Ropivacaína Kabi composition
- The active ingredient is ropivacaine hydrochloride 7.5 mg/ml. Each 10 ml polypropylene ampoule contains 75 mg of ropivacaine (hydrochloride).
Each 20 ml polypropylene ampoule contains 150 mg of ropivacaine (hydrochloride).
- The excipients are sodium chloride, hydrochloric acid (for pH adjustment), sodium hydroxide (for pH adjustment), and water for injectable preparations.
Product appearance and container contents
Ropivacaína Kabi injectable solution is a clear and colorless solution for injection.
Ropivacaína Kabi 7.5 mg/ml injectable solution is available in 10 ml and 20 ml transparent polypropylene ampoules.
Package sizes:
1, 5, and 10 ampoule(s)
1, 5, and 10 ampoule(s) in blister packaging
Only some package sizes may be marketed.
Marketing authorization holder and manufacturer
Marketing authorization holder
Fresenius Kabi España S.A.U.
C/ Marina 16-18
08005 Barcelona
Spain
Manufacturer
HP Halden Pharma AS
Svinesundsveien 80
1788 Halden
Norway
This medicinal product is authorized in the Member States of the European Economic Area and in the United Kingdom (Northern Ireland) under the following names:
Netherlands | Ropivacaïne Fresenius Kabi 7,5 mg/ml solution for injection |
Austria | Ropivacainhydrochlorid Kabi 7,5 mg/ml injection solution |
Belgium | Ropivacaïne Fresenius Kabi 7,5 mg/ml solution for injection/injectable solution/injection solution |
Bulgaria | Ropivacain Kabi 7,5 mg/ml, ??????????? ??????? |
Cyprus | Ropivacaine Kabi 7,5 mg/ml, εν?σιμο δι?λυμα |
Germany | Ropivacainhydrochlorid Kabi 7,5 mg/ml injection solution |
Denmark | Ropivacaine Fresenius Kabi, injection fluid, solution, 7.5 mg/ml |
Estonia | Ropivacaine Kabi |
Greece | Ropivacaine Kabi 7,5 mg/ml, εν?σιμο δι?λυμα |
Spain | Ropivacaina Kabi 7,5 mg/ml injectable solution EFG |
Finland | Ropivacain Fresenius Kabi 7,5 mg/ml injection fluid, solution |
France | Ropivacaïne Kabi 7,5 mg/ml, injectable solution |
Hungary | Ropivacaine Fresenius Kabi 7,5 mg/ml solution for injection |
Ireland | Ropivacaine 7.5 mg/ml solution for injection |
Italy | Ropivacaina Kabi |
Latvia | Ropivacaine Kabi 7,5 mg/ml solution for injection |
Lithuania | Ropivacaine hydrochloride Kabi 7,5 mg/ml injectable solution |
Luxembourg | Ropivacaïne Fresenius Kabi 7,5 mg/ml injection solution |
Malta | Ropivacaine Kabi 7,5 mg/ml |
Norway | Ropivacain Fresenius Kabi 7,5 mg/ml injection fluid, solution |
Poland | Ropivacaine Kabi |
Portugal | Ropivacaína Kabi |
Slovenia | Ropivakainijev klorid Kabi 7,5 mg/ml solution for injection |
Sweden | Ropivacain Fresenius Kabi 7,5 mg/ml, injection fluid, solution |
United Kingdom (Northern Ireland) | Ropivacaine 7.5 mg/ml solution for injection |
Date of the last revision of this leaflet: November 2024
“Detailed and updated information on this medicinal product is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS)http://www.aemps.gob.es/”
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This information is intended only for healthcare professionals:
Handling
Ropivacaína Kabi should only be used by, or under the supervision of, clinical personnel with experience in regional anesthesia (see section 3).
Shelf life after opening
Use immediately.
Ropivacaína Kabi products are intended for single use. Discard any unused solution.
The medicinal product should be visually inspected before use. The solution should only be used if it is clear, practically free of particles, and if the container is not damaged.
The intact container should not be re-autoclaved.
Incompatibilities
In the absence of compatibility studies, this medicinal product should not be mixed with others.
Precipitation may occur in alkaline solutions, as ropivacaine shows poor solubility at pH > 6.0.
Disposal
Disposal of unused medicinal products and all materials that have come into contact with them should be carried out in accordance with local regulations.
- Country of registration
- Dosage formINJECTABLE, 7.5 mg/ml
- ATC codeN01BB09
- Availability in pharmacies
Supply issue reported
Data from the Spanish Agency of Medicines (AEMPS) indicates a supply issue affecting this medicine.<br><br>Availability may be limited in some pharmacies.<br><br>For updates or alternatives, consult your pharmacist. - Active substance
- Prescription requiredYes
- Manufacturer
- This information is for reference only and does not constitute medical advice. Always consult a doctor before taking any medication. Oladoctor is not responsible for medical decisions based on this content.
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