Leaflet: Information for the user
Diclokern 11.6 mg/g gel
Diclofenac diethylamine
Read the entire leaflet carefully before starting to use this medication because it contains important information for you.
Follow exactly the administration instructions of the medication contained in this leaflet or as indicated by your doctor or pharmacist.
Contents of the leaflet:
The diclofenac diethylamine, the active ingredient of this medication, belongs to the group of non-steroidal anti-inflammatory drugs and acts as a local analgesic and anti-inflammatory.
Diclokern is indicated in adults and adolescents over 14 years for the local relief of pain and inflammation, mild and occasional, caused by:
You should consult a doctor if it worsens or does not improve after 7 days.
If you think you may be allergic, consult your doctor.
Warnings and precautions
Consult your doctor or pharmacist before starting to use Diclokern.
Children and adolescents
This medication is not recommended for use in children and adolescents under 14 years old, as there is not enough data available on safety and efficacy.
Use of Diclokern with other medications
Tell your doctor or pharmacist if you are using, have recently used, or may need to use any other medication.
Pregnancy and breastfeeding
If you are pregnant or breastfeeding, think you may be pregnant, or plan to become pregnant, consult your doctor or pharmacist before using this medication.
Pregnancy
Do not use Diclokern if you are in the last 3 months of pregnancy. Do not use Diclokern during the first 6 months of pregnancy, unless it is strictly necessary and recommended by your doctor. If you need treatment during this period, you should take the minimum possible dose for the shortest possible time.
Oral formulations (e.g., tablets) of diclofenac may cause adverse reactions to the fetus. It is not known if this same risk applies to Diclokern when used on the skin.
Breastfeeding
Consult your doctor or pharmacist before using any medication.
During breastfeeding, do not use Diclokern, unless your doctor has indicated it.
In no case should it be applied directly to the breast area.
Driving and using machines
No effects on the ability to drive vehicles and use machinery have been described when used externally on the skin.
Diclokern contains propylene glycol (E-1520)
This medication contains 50 mg of propylene glycol per gram of gel.
Follow exactly the administration instructions of the medication contained in this leaflet or as indicated by your doctor. In case of doubt, ask your doctor or pharmacist.
This medication is for application on the skin (cutaneous use).
The recommended dose is:
Adults and adolescents over 14 years:Apply 3 or 4 times a day a small amount of gel to the inflamed or painful area.
The amount of gel will vary depending on the size of the affected area (usually, it will be sufficient to apply an amount similar to the size of a cherry or a walnut).
Use in children and adolescents
This medication is not recommended for use in children and adolescents under 14 years old, as there is not enough data available on safety and efficacy.
Mode of use:
If the pain or swelling worsens or persists after 7 days of treatment, consult your doctor.
If you use more Diclokern than you should
If you accidentally ingest Diclokern or if you have used it on a large area of the skin and for a long period, adverse reactions similar to those produced by diclofenac when taken orally (e.g., tablets) may occur.
The main symptoms of overdose are: gastrointestinal or renal disorders and difficulty breathing, nausea, vomiting, abdominal pain, and decreased level of consciousness
If you have applied too much of the medication, it is recommended to eliminate it by washing the affected area with plenty of water, or by removing a part.
In case of accidental ingestion, go immediately to a medical center or call the Toxicology Information Service, phone: 91 562 04 20, indicating the medication and the amount ingested.
If you forget to use Diclokern
If you forget to apply this medication when it was due, apply the gel as soon as possible and continue the treatment normally.
Do not apply a double dose to make up for the forgotten doses.
If you interrupt treatment with Diclokern
If you have any other doubts about the use of this product, ask your doctor or pharmacist.
Like all medications, this medication can cause side effects, although not everyone will experience them.
Some rare and very rare side effects can be serious:
If you experience any of the following signs of allergy, stop using Diclokern and consult your doctor or pharmacist immediately:
Non-serious side effects:
Other side effects may occur, but they are usually mild and transient. If you notice any of them, consult your doctor or pharmacist as soon as possible.
Reporting of side effects
If you experience any type of side effect, consult your doctor or pharmacist, even if it is a possible side effect that does not appear in this leaflet. You can also report them directly through the Spanish Medication Surveillance System 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.
Do not store at a temperature above 30°C.
Do not use this medication after the expiration date that appears on the packaging after "CAD". The expiration date is the last day of the month indicated.
Once opened, discard the tube with the remaining gel after 12 months.
Medications should not be thrown away through the sewers or in the trash. Deposit the packaging and medications you no longer need in the SIGRE Point of the pharmacy. If in doubt, ask your pharmacist how to dispose of the packaging and medications you no longer need. This way, you will help protect the environment.
Composition of Diclokern
Appearance of the product and package contents
Diclokern is a viscous and white gel. It is packaged in an aluminum tube with a screw cap.
The medication is presented in a tube with 60 and 100 grams of gel.
Only some package sizes may be marketed.
Marketing authorization holder and manufacturer
Kern Pharma, S.L.
Venus, 72 - Pol. Ind. Colón II
08228 Terrassa - Barcelona
Spain
Date of the last revision of this leaflet: September 2019
Detailed and updated information on this medication is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.gob.es/.
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