Label: Information for the Patient
MEROPENEM SUN 1 g POWDER FOR INJECTABLE SOLUTION AND FOR IV INFUSION EFG
(meropenem trihydrate)
Read this label carefully before starting to use this medication, as it contains important information for you.
- Keep this label, as you may need to read it again.
- If you have any questions, consult your doctor, pharmacist, or nurse.
- This medication has been prescribed only for you and should not be given to others even if they have the same symptoms as you, as it may harm them.
- If you experience any adverse effects, consult your doctor, pharmacist, or nurse, even if they are not listed in this label. See section 4.
1. What Meropemen is and for what it is used
2. What you need to know before using Meropemen
3. How to use Meropemen
4. Possible adverse effects
5. Storage of Meropemen
6. Contents of the package and additional information
Meropenem belongs to a group of medications known as carbapenem antibiotics.
Antibiotics are used to treat bacterial infections and are not effective in treating viral infections such as the flu or common cold.
It is essential to follow the instructions regarding dosage, administration interval, and treatment duration provided by your doctor.
Do not store or reuse this medication. If you have any leftover antibiotic after treatment, return it to the pharmacy for proper disposal. Do not dispose of medications through the drain or trash.
It works by destroying bacteria that can cause severe infections.
Meropenem is used to treat the following infections in adults and children aged 3 months and older:
??Lung infection (pneumonia)
??Respiratory and lung infections in patients with cystic fibrosis
??Complicated urinary tract infections
??Complicated abdominal infections
??Infections that you may acquire during and after childbirth
??Complicated skin and soft tissue infections
??Acute bacterial infection of the brain (meningitis)
Meropenem may be used to treat patients with neutropenia who have fever suspected to be due to a bacterial infection.
Meropenem can be used to treat bacterial blood infection that may be associated with one of the previously mentioned infections.
Do not use Meropenem if
??You are allergic (hypersensitive) to meropenem or any of the other components of this medication (listed in section 6).
??You are allergic (hypersensitive) to other antibiotics such as penicillins, cephalosporins, or carbapenems, as you may also be allergic to meropenem.
Warnings and precautions
Consult your doctor, pharmacist, or nurse before using Meropenem if:
??You have health problems, such as liver or kidney problems.
??You have had severe diarrhea after taking other antibiotics.
You may develop a positive response to a test (Coombs test) indicating the presence of antibodies that can destroy red blood cells. Your doctor will discuss this with you.
You may develop signs and symptoms of severe skin reactions (see section 4). If this occurs, inform your doctor or nurse immediately so that they can treat the symptoms.
If you are in any of these situations, or if you have doubts, consult your doctor or nurse before using Meropenem.
Other medications and Meropenem
Inform your doctor, pharmacist, or nurse if you are using, have used recently, or may need to use any other medication, including those purchased without a prescription and herbal remedies.
This is because Meropenem may affect the way some medications work, and some of these may have an effect on Meropenem.
In particular, inform your doctor, pharmacist, or nurse if you are taking any of the following medications:
??Probenecid (used to treat gout).
??Valproic acid / sodium valproate / valpromide (used to treat epilepsy). Do not use Meropenem, as it may reduce the effect of sodium valproate.
??Oral anticoagulant (used to treat or prevent blood clots).
Pregnancy and breastfeeding
If you are pregnant or breastfeeding, or think you may be pregnant, consult your doctor or pharmacist before using this medication.
It is preferable to avoid using meropenem during pregnancy. Your doctor will decide whether to use meropenem.
It is essential to inform your doctor if you are breastfeeding or intend to breastfeed before receiving meropenem. Small amounts of this medication pass into breast milk. Therefore, your doctor will decide whether you should use meropenem during breastfeeding.
Driving and operating machinery
No studies have been conducted on the effects on the ability to drive and operate machinery.
However, Meropenem has been associated with headache, tingling or pins and needles in the skin (paresthesia); and involuntary muscle movements, leading to rapid and uncontrolled body agitation (convulsions), which is usually accompanied by loss of consciousness. Any of these effects may affect your ability to drive or operate machinery.
Meropenem contains sodium.
Meropenem 1 g:
This medication contains 90 mg of sodium (main component of table salt/for cooking) in each 1 g. This is equivalent to 4.5% of the maximum daily sodium intake recommended for an adult.
If you have a situation that requires controlling your sodium intake, inform your doctor, pharmacist, or nurse.
Follow exactly the administration instructions of this medication as indicated by your doctor or pharmacist. In case of doubt, consult your doctor or pharmacist again.
Use in adults
??The dose depends on the type of infection you present, the area of the body in which it is located, and its severity. Your doctor will decide what dose you need.
??The normal dose in adults is between 500 mg (milligrams) and 2 g (grams). Normally, you will be administered a dose every 8 hours. However, if your kidneys do not function well, you may receive the dose less frequently.
Use in children and adolescents
The dose for children over 3 months and up to 12 years is decided using the child's age and weight. The normal dose is between 10 mg and 40 mg of meropenem per kilogram (kg) of the child's weight. Normally, a dose is administered every 8 hours. Children weighing over 50 kg will be administered an adult dose.
How to use Meropenem
??Meropenem will be administered to you as an injection or infusion in a large-caliber vein.
??Meropenem will normally be administered by your doctor or nurse.
??However, some patients, parents, or caregivers are trained to administer meropenem at home. The instructions for this are found in this leaflet (in the section called "Instructions for administering meropenem to yourself or another person at home"). Follow exactly the administration instructions of Meropenem as indicated by your doctor. Consult your doctor if you have any doubts.
??Your injection should not be mixed with or added to solutions that contain other medications.
??The injection may take approximately 5 minutes or between 15 and 30 minutes. Your doctor will tell you how to administer Meropenem.
??Injections should normally be administered at the same time every day.
If you use more Meropenem than you should
If you accidentally use more doses than prescribed, contact your doctor or go to the nearest hospital immediately.
In case of overdose, accidental ingestion, or if you accidentally use more doses than prescribed, consult your doctor or pharmacist immediately or call the Toxicological Information Service, phone 91 562 04 20, indicating the medication and the amount ingested.
If you forget to use Meropenem
If you forget a dose, you should receive it as soon as possible. However, if it is almost time to administer the next dose, do not receive the missed one.
Do not use a double dose (two injections at once) to compensate for the missed dose.
If you interrupt the treatment with Meropenem
Do not stop Meropenem until your doctor tells you to.
If you have any other doubts about the use of this medication, ask your doctor or pharmacist.
Like all medicines, this medicine can cause side effects, although not everyone will experience them.
Severe allergic reactions
If you experience a severe allergic reaction,stop taking Meropenem and seek medical attention immediately. You may need urgent medical treatment. Symptoms may include a sudden onset of:
??Severe skin rash, itching, or hives.
??Swelling of the face, lips, tongue, or other parts of the body.
??Shortness of breath, wheezing, or difficulty breathing.
Blood cell damage (unknown)
Symptoms include:
??Shortness of breath when not expected.
??Red or brown urine.
If you notice anything of the above,seek medical attention immediately.
Other possible side effects:
Frequent (may affect up to 1 in 10 people)
??Abdominal pain (stomach).
??Nausea.
??Vomiting.
??Diarrhea.
??Headache.
??Skin rash, itching skin.
??Pain and inflammation.
??Increased platelet count in the blood (checked in a blood test).
??Changes in blood test results, including tests that show how well your liver is functioning.
Infrequent (may affect up to 1 in 100 people)
??Changes in your blood. These include a decrease in platelet count (which may make you bruise more easily), increased levels of some white blood cells, decreased levels of other white blood cells, and increased levels of a substance called “bilirubin”. Your doctor may perform blood tests periodically.
??Changes in blood test results, including tests that show how well your kidneys are functioning.
??Tickling sensation (tingling).
?Infections of the mouth or vagina caused by a fungus (thrush).
?Intestinal inflammation with diarrhea.
?Pain in the veins where Meropenem is injected.
?Other changes in your blood. Symptoms include frequent infections, fever, and sore throat. Your doctor may perform blood tests periodically.
Rare (may affect up to 1 in 1000 people)
??Seizures.
??Acute disorientation and confusion (delirium).
Reporting side effects:
If you experience any type of side effect, consult your doctor, pharmacist, or nurse, even if it is a possible side effect that does not appear in this leaflet. You can also report them directly through the Spanish System for Pharmacovigilance of Medicines for Human Use:https://www.notificaram.es. By reporting side effects, you can contribute to providing more information on the safety of this medicine.
Keep this medication out of the sight and reach of children.
Do not use this medication after the expiration date that appears on the label and on the box after CAD. The expiration date is the last day of the month indicated.
Do not store at a temperature above25°C.
After reconstitution: Reconstituted solutions for intravenous injection or infusion must be used immediately. The time interval between the start of reconstitution and the end of intravenous injection or infusion should not exceed one hour.
Do not freeze the reconstituted solution.
Medicines should not be thrown away through drains or in the trash. Ask your pharmacist how to dispose of the containers and medicines you no longer need. This will help protect the environment.
Composition of Meropenem
The active ingredient is meropenem trihydrate.
Each vial contains meropenem trihydrate equivalent to 1 g of anhydrous meropenem.
The other component is anhydrous sodium carbonate.
Appearance of the product and contents of the container
Meropenem is a white to light yellow powder, for injection or infusion solution in vial. Container sizes of 1 or 10 vials.
Only some container sizes may be commercially available.
Marketing Authorization Holder and Responsible Person for Manufacturing
Marketing Authorization Holder
Sun Pharmaceutical Industries Europe B.V.,
Polarisavenue 87,
2132JH Hoofddorp, Netherlands
Responsible Person for Manufacturing
TERAPIA S.A.
124 Fabricii Street
400 632 Cluj Napoca
Romania
Or
Sandoz GmbH
Biochemiestraße 10
A-6250 Kundl
Austria
Or
Basics GmbH
Hemmelrather Weg 201
D-51377 Leverkusen
Germany
Local Representative
Sun Pharma Laboratorios,S.L.
Rambla de Catalunya, 53-55
08007 Barcelona.
Spain
Tel.: +34 93 342 78 90
This medicinal product is authorized in the Member States of the European Economic Area under the following names:
Spain: Meropenem SUN 1 g powder for solution for injection or infusion EFG.
Northern Ireland: Meropenem 1 g powder for solution for injection or infusion
Date of the last revision of this leaflet: March 2021.
The detailed and updated information on this medicinal product is available on the website of the Spanish Agency for Medicines and Medical Devices (AEMPS) http://www.aemps.gob.es
Healthcare advice/education
Antibiotics are used to treat infections caused by bacteria. They have no effect on infections caused by viruses.
Occasionally, an infection caused by a bacterium does not respond to treatment with an antibiotic. One of the most common reasons for this to happen is that the bacteria causing the infection are resistant to the antibiotic being taken. This means that they can survive and even multiply, despite the antibiotic.
Bacteria can become resistant to antibiotics for many reasons. Using antibiotics with caution can help reduce the opportunity for bacteria to become resistant to them.
When your doctor prescribes a treatment with an antibiotic, it is to treat only your current illness. Paying attention to the following advice will help prevent the appearance of resistant bacteria that could stop the antibiotic from working.
1. It is very important that you receive the correct dose of the antibiotic, the right number of times, and for the correct number of days. Read the instructions on the leaflet and, if you do not understand something, consult your doctor or pharmacist to explain it to you.
2. Do not use an antibiotic unless you have been specifically prescribed it for you, and use it only to treat the infection for which it has been prescribed.
3. Do not use antibiotics that have been prescribed for other people, even if they have had a similar infection to yours.
4. Do not give antibiotics to other people that were prescribed for you.
5. If you have any antibiotic left over after receiving the treatment as indicated by your doctor, take it to the pharmacy to be disposed of properly.
This information is intended solely for healthcare professionals:
Instructions for administering Meropenem yourself or to another person at home
Some patients, parents, and caregivers are trained to administer Meropenem at home.
Attention – You should only administer this medication to yourself or to another person at home after a doctor or nurse has trained you.
??The medication must be mixed with another liquid (the diluent). Your doctor will tell you what amount ofdiluent is used.
??Use the medication just after preparing it. Do not freeze it.
How to prepare this medication
1.Wash your hands and dry them very well. Prepare a clean work area.
2.Remove the vial (vial) of Meropenem from the packaging. Check the vial and the expiration date. Check that the vial is intact and not damaged.
3.Remove the colored cap and clean the grey rubber stopper with an alcohol-soaked cotton swab. Let the stopper dry.
4.Insert a new sterile needle into a new sterile syringe, without touching the ends.
5.Extract the recommended amount of "Intravenous Injection Water" with the syringe. The amount of liquid needed is shown in the table below:
Dose of Meropenem | Amount of "Intravenous Injection Water" needed for dilution |
500 mg (milligrams) | 10 ml (milliliters) |
1 g (gram) | 20 ml |
1.5 g | 30 ml |
2 g | 40 ml |
Take note that:If the amount of Meropenem prescribed to you is greater than1 g, you will need to use more than one vial of Meropenem. You can then extract the liquid from the vials in a syringe.
6.Pierce the center of the grey rubber stopper with the needle of the syringe and inject the recommended amount of "Intravenous Injection Water" into the/ the vial/s of Meropenem.
7.Remove the needle from the vial and shake it well for about 5 seconds, or until all the powder has dissolved. Clean the grey rubber stopper again with a new alcohol-soaked cotton swab and let it dry.
8.With the plunger of the syringe pushed all the way in, pierce the grey rubber stopper again with the needle. You should then hold the syringe and the vial and turn the vial upside down.
9.Keeping the end of the needle in the liquid, pull the plunger and extract all the liquid from the vial into the syringe.
10.Remove the needle and syringe from the vial and dispose of the empty vial in an appropriate container.
11.Hold the syringe vertically, with the needle pointing upwards. Give the syringe gentle taps to allow any bubbles in the liquid to rise to the top of the syringe.
12.Remove the air from the syringe by gently pushing the plunger until the air has come out.
13.If you are using Meropenem at home, dispose of the needles and infusion lines you have used properly. If your doctor decides to stop your treatment, dispose of the Meropenem you have not used properly.
Administration of the injection
You can administer this medication through a peripheral intravenous catheter, or through a central port or line.
Administration of Meropenem through a peripheral intravenous catheter
1. Remove the needle from the syringe and dispose of it properly in your authorized sharp objects containers.
2. Clean the end of the peripheral intravenous catheter with an alcohol-soaked cotton swab and let it dry. Open the cap of the cannula and connect the syringe.
3. Press the plunger of the syringe slowly to administer the antibiotic at a constant rate for about 5 minutes.
4. Once you have finished administering the antibiotic and the syringe is empty, remove it and clean the site as recommended by your doctor or nurse.
5. Close the cap of the cannula and dispose of the syringe properly in your authorized sharp objects containers.
Administration of Meropenem through a central port or line
1. Remove the cap from the central port or line, clean the end with an alcohol-soaked cotton swab and let it dry.
2. Connect the syringe and press the plunger slowly to administer the antibiotic at a constant rate for about 5 minutes.
3. Once you have finished administering the antibiotic, remove the syringe and clean the site as recommended by your doctor or nurse.
4. Place a new clean cap on the central port or line and dispose of the syringe properly in your authorized sharp objects containers.
Administration of Meropenem through intravenous infusion
Meropenem can be administered through intravenous infusion over approximately15 to30 minutes.The vials for intravenous infusion of meropenem can be reconstituted directly with sodium chloride 9 mg/ml (0.9%) or glucose 50 mg/ml (5%) solutions, to a final concentration of1 to20 mg/ml.
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