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Hexal Diclac pain gel 1%

Hexal

AED 81.00
+ AED 46.00 Air Shipping

Includes any applicable VAT and customs duty.
Air shipping cost to be recalculated with delivery address at checkout.
To be delivered in 6 - 9 * working days.
100% genuine and new product.
Credit card / Cash on Delivery

Description

Diclac pain gel 1%
provider: hexal AG
dosage form: gel
50 g | PZN: 03424835
100 g | PZN: 03424841
150 g | PZN: 05388026
active ingredient: diclofenac sodium
Read the package insert and ask your doctor or pharmacist.
Important information (mandatory information):
diclac pain gel 1% gel.
active ingredient: diclofenac sodium. Areas of application: In adults for external treatment of pain, inflammation and swelling in sports and accident injuries (sprains, bruises, strains), rheumatic diseases of the soft tissues (tendon and tendonal inflammation, bursitis, inflammation in the muscle and capsule area) and in degenerative diseases of the peripheral extremities joints. In adolescents aged 14 and over for short -term treatment for local, symptomatic treatment of pain in acute bruises, strains or sprains due to a blunt trauma.
Use information: Information for the user
diclac pain gel 1% gel for adults and adolescents from the age of 14
active ingredient: diclofenac sodium
Read the entire package supplement carefully before using this medicine Start because it contains important information. Always use this medicine as described in this package insert or exactly according to your doctor or pharmacist.
Use the package insert. You might want to read it again.
Ask your pharmacist if you need more information or advice.
If you notice side effects, contact your doctor or pharmacist. This also applies to side effects that are not specified in this package insert. See section 4.
If you don't feel better or worse after 3-5 days, please contact your doctor.
What in this package insert:
What is diclac pain gel and what is it used for?
What should you consider before using diclac pain gel?
How is diclac pain gel to be used?
What side effects are possible?
How is diclac pain gel to be kept?
Content of the pack and further information
1. What is diclac pain gel and what is it used for?
Diclac pain gel contains an active ingredient from the group of so-called non-steroidal anti-phlogistics/analgesics (inflammatory and pain inhibitors) with diclofenac sodium.
area of application in adults:
diclac pain gel is used to externally treat pain, inflammation and swelling in sports and accident violations (sprains, bruises, strains), rheumatic diseases of the soft tissues (tendon and tendonal inflammation, bleeding, inflammation in Muscle and capsule area) and with degenerative diseases of the peripheral extremities joints.
Area of application for adolescents from the age of 14:
for short -term treatment for local, symptomatic treatment of pain in acute bruises, strains or sprains due to a blunt trauma.
2. What should you consider before using diclac pain gel?
diclac pain gel must not be used,
if you allergic to diclofenac, soy, peanut, 2-benzyliden hept anal, citronellol, benzyl (2-hydroxybenzoat), geraniol, rac- (1r) -4- (4-hydroxy -4-methylpentyl) CycloHex-3-en-1-carbaldehyde, 7-hydroxy-3,7-dimethyloctanal, 2- (4-tert-butylbenzyl) propanal or one of the other components of this drug mentioned in section 6.
If you have reacted in the past with breathing problems (asthma, bronchospasm), skin reactions (hives), running nose or swelling of the face or tongue after taking/using acetylsalicylic acid or another non-steroidal anti-inflammatory drug (e.g. ibuprofen) .
on open injuries, inflammation or infections of the skin as well as on eczema or mucous membranes.
In the last third of the pregnancy.
In children and adolescents under the age of 14.
Warnings and precautions:
Please speak to your doctor or pharmacist before using Diclac pain gel. If Diclac pain gel is applied extensively to the skin and applied over a longer period of time, the occurrence of side effects that affect a certain organ system or the entire organism cannot be ruled out. These side effects are comparable to those that may occur when taking other diclofenac-containing medicines. Diclac pain gel does not apply for a long time or in higher doses than the specified. Diclac pain gel may only be applied to intact, non -sick or injured skin and not to open wounds. The eyes and mucous membranes must not come into contact with the medicine and it must not be taken. If Diclac pain gel gets into her eyes, rinse them carefully with water. Consult your doctor or pharmacist if the symptoms stop. You can use an association, but no occlusal association (densely final association). Before putting on an association, Diclac pain gel should dry on the skin for a few minutes.
Special caution in the application is necessary for acute conditions that are associated with strong redness, swelling or overheating of joints. In the event of ongoing joint complaints or in the case of violent back pain that radiate into the legs and/ or are connected with neurological failure (e.g. numbness, tingling), a doctor should be consulted. In the event of complaints that have not improved or worsen after 3-5 days, you should see a doctor. If you suffer from asthma, hay fever or nasal mucosal swelling (so-called nasal polyps) or chronic, bronchy-compatible (obstructive) respiratory diseases, chronic respiratory infections (particularly coupled with hay fever-like phenomena) or hypersensitivity to other pain and rheumatism. Pain gel caused by asthma attacks (so-called analgesic intolerance/analgesics), local skin and mucosal swelling (so-called quinc-edema) or hives (urticaria) rather endangered than other patients. In this case, Diclac pain gel may only be used under certain precautionary measures (emergency willingness) and direct medical control. The same applies if you also react hypersensively against other substances, such as with skin reactions, itching or nettle fever.
If a rash occurs during treatment with Diclac pain gel, end the treatment. During the treatment, the sensitivity to light can occur with the occurrence of skin symptoms after exposure to light. It should be ensured that children with their hands do not come into contact with the grated skin areas.
Children and adolescents:
diclac pain gel must not be used in children and adolescents under the age of 14, since there is no sufficient experiences for this age group.
Use of diclac pain gel together with other medicinal products:
inform your doctor or pharmacist if you take/use other medicines, recently taken/use other medicines or intend to accept/apply other medicines. So far, no interactions have become known for intended, external use of Diclac pain gel.
pregnancy and lactation:
If you are pregnant or breastfeed, or if you suspect that you are pregnant or intend to become pregnant, ask your doctor or pharmacist for advice before using this medicine.
pregnancy:
In the first and second third of pregnancy, Diclac pain gel should only be used after consultation with the doctor. In the last third of the pregnancy you must not use Diclac pain gel because an increased risk of complications for mother and child cannot be ruled out.
breastfeeding:
diclofenac passes into breast milk in small quantities. Diclac pain gel should only be used after consultation with the doctor. The drug should not be applied to large other skin areas in the chest area or over a longer period of time.
Road and ability to use machines:
Diclac pain gel has no or an excessive influence on the traffic and the ability to use machines.
diclac pain gel contains a fragrance with allergens:
This medicine contains a fragrance with 2-benzylid hept anal, citronellol, benzyl (2-hydroxybenzoat), geraniol, rac- (4-hydroxy-4- Methylpentyl) CycloHex-3-en-1-carbaldehyde, 7-hydroxy-3,7-dimethyloctanal, 2- (4-tert-butyl-benzyl) propanal. These can cause allergic reactions.
3. How is diclac pain gel to be applied?
Always use this medicine as described in this package insert or exactly according to your doctor or pharmacist. Ask your doctor or pharmacist if you are not sure.
The recommended dose is:
Adults and adolescents from the age of 14:
Depending on the size of the painful area to be treated, a cherry to walnut-sized amount is 1-4 g (10-40 mg diclofenac- Sodium), required. The maximum total daily dose is 16 g gel, according to 160 mg diclofenac sodium. Unless otherwise prescribed by the doctor, Diclac pain gel is used 3 to 4 times a day. In the event of complaints that have not improved or worsened after 3-5 days, a doctor should be consulted. Please speak to your doctor or pharmacist if you have the impression that the effect of Diclac pain gel is too strong or too weak.
older patients:
No special dose adjustment is required. However, older patients should pay particular attention to side effects when using and, if necessary, consult their doctor or pharmacist.
restricted kidney or liver function:
no dose reduction is required.
Children and adolescents under the age of 14:
There is not sufficient data on effectiveness and tolerance in children and adolescents under the age of 14 (see section 2).
Young people aged 14 and over:
In young people aged 14 and older, the patient/parents are advised to see a doctor if the medicine is needed for more than 7 days for pain treatment or the symptoms deteriorate.
Duration of the application:
As a rule, depending on the symptoms and the underlying disease, an application over 1 - 2 weeks is sufficient. With a long -term application, you should see your doctor. This then decides depending on the indication and symptoms about the duration of use. Do not apply Diclac pain gel than necessary and only for the minimally required duration of use.
Type of application:
diclac pain gel is only intended for use on the skin. Do not take! Apply the diclac pain gel to the affected parts of the body thinly and rub it in slightly. It should not be rubbed with pressure. Then the hands should be washed, unless these are the area to be treated. Before putting on an association, Diclac pain gel should dry on the skin for a few minutes. The application of a densely final association is not recommended. To support the penetration of the active ingredient, the use of diclac pain gel is possible using ondophoresis. Diclac pain gel must be applied under the cathode (negatively charged electrode).
If you have applied a larger amount of diclac pain gel than you should:
due to the low inclusion of diclofenac to the overall organism with limited use on the skin, overdose is unlikely. If the recommended dosage is clearly exceeded when using it on the skin, the gel should be removed and washed off with water. In the event of accidentally swallowing (e.g. also in children) from Diclac Pain Gel, please notify your doctor immediately, who will decide on suitable measures.
If you have forgotten the application of diclac pain gel:
don't apply twice the amount if you have forgotten the previous application.
If you have any further questions about the application of this medicine, please contact your doctor or pharmacist.
4. What side effects are possible?
Like all medicines, this medicine can also have side effects, but this does not have to occur with everyone. The following side effects can have serious consequences, do not apply Diclac pain gel and search your doctor as soon as possible:
rarely (can affect up to 1 out of 1,000):
skin inflammation with bladder formation (bullous dermatitis).
very rare (can affect up to 1 out of 10,000):
whistling breath, shortness of breath or feeling tight in the chest (asthma).
swelling of face, lips, tongue or throat (angio edema).
Further side effects are possible:
frequently (can affect up to 1 of 10 treated):
rash, eczema, reddening of the skin (erythema), dermatitis (including contact dermatitis), itching (pruritus).
Occasionally (can affect up to 1 out of 100):
scales, drying out the skin, swelling (edema).
very rare (can affect up to 1 out of 10,000):
Pustel -like rash.
gastrointestinal complaints.
hypersensitivity reactions (including hives).
Sensitivity to light with the occurrence of skin symptoms after exposure to light (photosensitization).
other possible side effects:
(3-SN phosphatidyl) choline (soy) can very rarely cause allergic reactions. The allergens 2-benzyliden heptanal, citronellol, benzyl (2-hydroxy-benzoat), geraniol, rac- (1r) -4- (4-hydroxy-4-methyl pentyl) cycloHex-3-1-carbaldehyde, 7 in the fragrance -Hydroxy 3,7-dimethyloctanal, 2- (4-tert-butyl-benzyl) propanal can cause allergic reactions. If diclac pain gel is applied extensively to the skin and applied over a longer period of time, the occurrence of systemic side effects (e.g. renal, hepatic or gastrointestinal side effects, systemic hypersensitivity reactions), as can occur after systemic use of diclofenac-containing medicines to exclude.
Announcement of side effects:
If you notice side effects, contact your doctor or pharmacist. This also applies to side effects that are not specified in this package insert. You can also directly see the Federal Institute for Medicines and Medical Devices, Pharmacovigilance, Kurt-Georg-Kiesinger-Allee 3, D-53175 Bonn, website: www.bfarm.de. By reporting side effects, you can help to provide more information about the safety of this drug.
5. How is diclac pain gel to be kept?
keep this medicine for children inaccessible. You can no longer use this medicine after the expiry date specified on the karton and the tube for "usable to" or "Use". The expiry date refers to the last day of the specified month.
storage conditions:
do not store above 25 ° C.
Note on durability after the approach:
After opening the tube for the first time, Diclac pain gel is for 9 months.
Never dispose of medicines via the waste water (e.g. not via the toilet or sink). Ask in your pharmacy how to dispose of the drug if you no longer use it. You help to protect our environment. Further information can be found at www.bfarm.de/arzneimstimmittelgung.
6. Content of the pack and further information
What diclac pain gel contains:
The active ingredient is diclofenac sodium. 1 g of gel contains 10 mg diclofenac sodium. The other components are: ammonia, carbomer (980), decyloleate, sodium defeat (ph.eur.), Octildodecanol (Ph.Eur.), (3-Sn-Phosphatidyl) Cholin (soy), 2-propanol (Ph.Eur. ), all-rac-alpha-tocopherol, fragrance (contains 2-benzyliden heptanal, citronellol, benzyl (2-hydroxy-benzoat), geraniol, rac- (1r) -4- (4-hydroxy-4-methylpentyl) cyclohex-3 -en-1-carbaldehyde, 7-hydroxy-3,7-dimethyloctanal, 2- (4-tert-butyl-benzyl) propanal), cleaned water.
what Diclac pain gel looks like and contents of the pack:
slightly yellowish, smooth, homogeneous liposome emulsion gel. Diclac pain gel is available in packs with 50 g, 100 g and 150 g gel. Not all package sizes may be placed on the market.
Pharmaceutical entrepreneur:
Hexal AG
Industriestrasse 25
83607 Holzkirchen
Telephone: (08024) 908-0
fax: (08024) 908-1290
E-mail: Service@hexal.com
Manufacturer
Salutas Pharma GmbH
Otto von-Guericke-Allee 1
39179 Barleben
This use information was last revised in January 2021.
Source: Package insert
Stand: 09/2021
Made by: Hexal AG
Areas of application
- Pain, swelling and inflammation of the musculoskeletal system, as with: - Swelling and inflammation of the soft tissue close to the joints (e.g. from bursa, tendon sheaths, Bands, inflammation in the muscle and capsule area) - osteoarthritis, especially the large joints - sports and accident injuries, such as: - bruises - sprains and strains
diclofenac sodium, diclofenac, ammonia, carbomer 980, decyloleate, Dinatrium Edetat-2-Wasser, Octylldodecanol, Plantlezithin, Isopropanol,
-scopherol, odor correct, 2-benzylid heptanal, citronellol, benzyl salicylate, geraniol, (
) -4- (4-hydroxy-4-methylpentyl ) CycloHex-3-Encarbaldehyde, 7-hydroxy-3,7-dimethyloctanal, 2- (4-
tert
butylbenzyl) propanal, water, cleaned
gel
application information < BR> The total dose should not be exceeded without consulting a doctor or pharmacist.
Type of application?
Apply the medicine to the person concerned. Then massage the medicine. Wash your hands thoroughly after use. Avoid accidental contact with mucous membranes, eyes and open skin areas.
duration of the application?
Usually an application over 1-2 weeks is sufficient. You should see your doctor in the event of long -lasting complaints. In the event of complaints that have not improved or worsened after 3-5 days, a doctor should be consulted. Without medical advice, young people should not apply the drug for more than 7 days.
overdosing?
If the drug is used as described, no overdose symptoms are known. If in doubt, contact your doctor. The following applies
: Pay particular attention to a conscientious dosage in infants, toddlers and older people. If in doubt, ask your doctor or pharmacist about any effects or precautionary measures.
A dosage prescribed by the doctor may differ from the information on the package insert. Since the doctor coordinates you individually, you should therefore apply the medicine according to his instructions.
mode of action
How does the ingredient of the drug work?
The active ingredient has a pain reliever, fever -lowering and anti -inflammatory at the same time. The drug also has antirheumatic properties. He blocks the formation of certain messenger substances in the body, so -called prostaglandins. These are significantly involved in the development of pain, fever and inflammation.
Contraindications
What speaks against an application?
Always:
- hypersensitivity to the ingredients
Under certain circumstances - speak to your doctor or pharmacist:
- spontaneously occurring (mucus) skin swelling (angioedema)
- nettle rash ( Urticaria)
- chronic obstructive respiratory disease (chronic respiratory disease with a narrowing of the respiratory tract)
- chronic respiratory infections
- asthma bronchial
- allergic runny nose, for example hay fever
nasal polyp (nasal mucosa growth)
- eczema
- open injuries, inflammation or infections of the skin
Which age group must be observed?
- children under the age of 14: The drug must not be used.
- Children and adolescents under the age of 18: In this age group, the drug should only be used in certain areas of application. Please ask your doctor or pharmacist, if you have questions regarding this topic.
What about pregnancy and breastfeeding?
- pregnancy: contact your doctor. Different considerations play a role in whether and how the medicine can be used during pregnancy.
- breastfeeding: contact your doctor or pharmacist. He will check your special starting position and advise you accordingly whether and how you can continue with breastfeeding.
If you have been prescribed the medicine despite a counter -notification, speak to your doctor or pharmacist. The therapeutic benefit can be higher than the risk of using a counter -notification.
Side effects
What undesirable effects can occur?
- Super sensitivity reactions of the skin, such as:
- rash
- eczema
- reddening of the skin
- inflammatory reactions of the skin
- contact dermatitis (allergic skin reactions that only occur when used)
- itching
- scale formation of the skin
- drying out the skin
- water retention (edema)
If you notice a state of state or change during treatment, contact your doctor or pharmacist.
For information at this point, side effects are taken into account that occurs in at least one of 1,000 patients treated.
Important information
What should you consider?
- Caution: patients with nasal polyps, chronic respiratory infections, asthma or with a tendency to allergic reactions such as hay fever: for them, the medicine can trigger a asthma attack or a strong allergic skin reaction. Therefor consult your doctor before usage.
- be careful with allergy to painkillers!
- be careful with allergy against peanuts and soy.
package insert
package insert

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product quantity : 150 g

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Hexal Diclac pain gel 1%

AED 81.00
+ AED 46.00 Air Shipping

Includes any applicable VAT and customs duty.
Air shipping cost to be recalculated with delivery address at checkout.
To be delivered in 6 - 9 * working days.
100% genuine and new product.
Credit card / Cash on Delivery

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The following are the refund timeliness associated with each payment method.

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