Ask a doctor about a prescription for PANTOMICINA 1g POWDER FOR SOLUTION FOR INFUSION
Package Leaflet: Information for the User
Pantomicina 1g Powder for Solution for Infusion
erythromycin lactobionate
Read all of this leaflet carefully before you start using this medicine because it contains important information for you.
Contents of the Package Leaflet
Pantomicina 1g Powder for Solution for Infusion contains the active substance erythromycin lactobionate, an antibiotic belonging to a group called macrolides.
Antibiotics are used to treat bacterial infections and are not effective against viral infections such as flu or the common cold. It is essential to follow the instructions regarding dosage, administration interval, and treatment duration as indicated by your doctor. Do not store or reuse this medicine. If you have any leftover antibiotic after completing treatment, return it to the pharmacy for proper disposal. Do not throw medicines down the drain or in the trash. |
Pantomicina 1g Powder for Solution for Infusion is indicated for the treatment of:
Do not use Pantomicina 1g Powder for Solution for Infusion
Warnings and Precautions
Consult your doctor, pharmacist, or nurse before starting to use Pantomicina 1g Powder for Solution for Infusion:
Children
If a baby or child is receiving antibiotics and is irritable or vomits when feeding, you should inform your doctor immediately. There is a risk that the child may develop a severe stomach disorder called pyloric stenosis.
Using Pantomicina 1g Powder for Solution for Infusion with other medicines
Tell your doctor, pharmacist, or nurse if you are using, have recently used, or might use any other medicine.
It is especially important that you inform them if you are taking any of the following medicines and treatments.
This is also important if you are taking medicines called:
The administration of Pantomicina 1g Powder for Solution for Infusion may increase the effect of:
The following medicines may reduce the effect of Pantomicina 1g Powder for Solution for Infusion:
The administration of Pantomicina 1g Powder for Solution for Infusion may decrease the effect of:
The use of Pantomicina 1g Powder for Solution for Infusion along with calcium channel blockers, such as verapamil, can cause a drop in blood pressure, a decrease in heart rate, or acidification of the blood.
The use of Pantomicina 1g Powder for Solution for Infusion along with cimetidine (a medicine used to treat ulcers) can cause an increase in Pantomicina levels in the blood.
Pregnancy, Breastfeeding, and Fertility
If you are pregnant or breastfeeding, think you may be pregnant, or are planning to have a baby, ask your doctor or pharmacist for advice before using this medicine.
Pantomicina 1g Powder for Solution for Infusion should only be used during pregnancy and breastfeeding if your doctor thinks it is necessary and follows their recommendations. The safety of erythromycin during pregnancy has not been established. Erythromycin crosses the placental membrane and also appears in breast milk.
Information from studies on the risk of congenital anomalies is not consistent, but some studies have reported cardiac anomalies after the use of Pantomicina 1g Powder for Solution for Infusion at the beginning of pregnancy. It is essential to use effective contraceptive methods during treatment with this medicine (see section "Using Pantomicina 1g Powder for Solution for Infusion with other medicines").
Driving and Using Machines
Treatment with Pantomicina has a mild influence on the ability to drive or use machines.
Follow the instructions for administration of this medicine exactly as indicated by your doctor. If you are in doubt, consult your doctor or pharmacist again. This medicine will always be administered by a doctor or nurse.
The recommended dose is
For the treatment of severe infections in adults and children, the recommended intravenous dose is 15 to 20 mg/kg/day. In cases of very severe infections, higher doses may be used, up to 4 g/day.
For the treatment of "Legionnaires' disease", although the optimal doses have not been established, the recommended doses, according to known clinical data, are 1 to 4 g per day in divided doses.
For the treatment of acute inflammatory disease of the pelvis caused by N. gonorrhoeaein women who are hypersensitive to penicillin, administer 500 mg of erythromycin lactobionate every 6 hours for 3 days, followed by 250 mg of erythromycin orally every 6 hours for 7 days.
Elderly Patients
Elderly patients usually require lower doses than adult patients. It is more likely that adverse reactions will occur in these patients. Your doctor will provide you with special information about the necessary precautions, doses, and follow-up.
If you are given more Pantomicina 1g Powder for Solution for Infusion than you should
No type of poisoning has been described with the intravenous administration of erythromycin. If hypersensitivity manifestations occur, treatment should be discontinued and appropriate therapy initiated: administration of adrenaline, steroids, etc.
In case of overdose or accidental ingestion, consult the Toxicology Information Service, phone: 91 562 04 20.
If you have any other questions about the use of this product, ask your doctor or pharmacist.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
Contact your doctor or pharmacist as soon as possible if you experience the following side effects:
The following side effects have been observed with the administration of this medicine:
Very common (may affect more than 1 in 10 people):
Stomach pain
Nausea
Vomiting
Diarrhea
Lack of appetite (anorexia).
Common (may affect up to 1 in 10 people):
Increased liver enzymes and bilirubin
Skin rash.
Uncommon (may affect up to 1 in 100 people):
Allergic reactions in the form of hives that cause intense itching.
Rare (may affect up to 1 in 1,000 people):
Reversible hearing loss*
Very rare (may affect up to 1 in 10,000 people):
Disorientation
Hallucinations
Seizures
Dizziness
Hearing noises in the ear (tinnitus)
State of confusion
Sensation of rotational movement (vertigo)
Frequency not known (cannot be estimated from the available data):
Low levels of white blood cells (eosinophilia)
Hallucinations
Visual impairment
Deafness
Drop in blood pressure (hypotension)
Itching
Chest pain
Pain at the injection site ***
Fever
Malaise.
** Hypertrophic pyloric stenosis in children
*** Sometimes venous irritation and pain have been found; if the infusion is administered slowly, preferably by continuous or intermittent intravenous infusion in no less than 20 to 60 minutes, this effect can be minimized.
If you think any of the side effects you are experiencing are serious or if you notice any side effects not mentioned in this leaflet, tell your doctor or pharmacist.
Reporting of Side Effects
If you experience any side effects, talk to your doctor or pharmacist, even if it is possible side effects not listed in this leaflet. You can also report them directly through the Spanish Pharmacovigilance System for Human Use Medicines: https://www.notificaram.es. By reporting side effects, you can help provide more information on the safety of this medicine.
Keep this medicine out of the sight and reach of children.
This medicine does not require special storage conditions.
Do not use this medicine after the expiry date which is stated on the packaging after the abbreviation EXP. The expiry date is the last day of the month shown.
Do not use this medicine if you notice that the packaging is damaged or shows signs of tampering.
Medicines should not be disposed of via wastewater or household waste. Place the packaging and any unused medicine in the SIGRE Pointof the pharmacy. If you are unsure, ask your pharmacist how to dispose of the packaging and any unused medicine. This will help protect the environment.
Composition of Pantomicina 1g powder for solution for perfusion
Appearance of the Product and Container Content
Liofilized powder for solution for perfusion in 1 sterile vial
Marketing Authorization Holder and Manufacturer
Holder:
Amdipharm Limited
Unit 17
Northwood House
Northwood Crescent
Northwood
Dublin 9
D09 V504
Ireland
Local Representative
Ferrer Internacional, S.A.
Gran Vía Carlos III, 94
08028 Barcelona, Spain
Manufacturer
DELPHARM SAINT REMY
Rue de l'Isle
Saint Remy sur Avre,
28380, – France
Date of the Last Revision of this Leaflet: February 2023
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/)
Discuss dosage, side effects, interactions, contraindications, and prescription renewal for PANTOMICINA 1g POWDER FOR SOLUTION FOR INFUSION – subject to medical assessment and local rules.