Diklak gel 5% 100g
Category
Bruises, sprains
Scope of the drug
Musculoskeletal system
Release form
Gel
Manufacturer country
Germany
Package quantity, pcs
one
Release form, composition and packaging
Gel for external use 5% colorless or slightly yellowish, transparent, homogeneous and free of bubbles, with a characteristic smell of isopropyl alcohol.
1 g
diclofenac sodium 50 mg
isopropanol (isopropyl alcohol), macrogol glyceryl cocoate (macrogol-7-glyceryl cocoate), hypromellose, aromatic oil, purified water.
50 g - aluminum tubes (1) - cardboard boxes.
100 g - aluminum tubes (1) - cardboard boxes.
pharmachologic effect
NSAIDs for external use.
It has a pronounced analgesic and anti-inflammatory effect.
By indiscriminately inhibiting COX-1 and COX-2, it disrupts the metabolism of arachidonic acid and the synthesis of prostaglandins, which are the main link in the development of inflammation.
In the area of application, Diklak eliminates pain and reduces swelling associated with the inflammatory process.
Pharmacokinetics
Data on the pharmacokinetics of Diclacne are provided.
Indications for use
- diseases of the musculoskeletal system: rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis, osteoarthritis of the peripheral joints and spine
- rheumatic lesions of soft tissues
- muscle pains of rheumatic and non-rheumatic origin
- traumatic injuries of soft tissues.
Contraindications for use
- aspirin" asthma
- violation of the integrity of the skin
- III trimester of pregnancy
- lactation period (breastfeeding)
- children under 6 years old
- hypersensitivity to drug components
- hypersensitivity to acetylsalicylic acid or other NSAIDs.
The drug should be used with caution in hepatic porphyria (exacerbation), erosive and ulcerative lesions of the gastrointestinal tract, severe liver and kidney dysfunction, in chronic heart failure, in bronchial asthma, in elderly patients, in the first and second trimesters of pregnancy.
Dosage regimen
The drug is used externally.
For adults and children over 6 years old, the drug is applied to the skin and rubbed lightly, the frequency of application is 2-3 times / day.
The required amount of the drug depends on the size of the affected area.
A single dose of the drug is up to 2 g (about 4 cm with a completely open tube mouth).
Wash your hands after applying the drug.
The duration of treatment depends on the indications and the observed effect.
After 2 weeks of using the drug, the patient should consult a doctor.
Overdose
The extremely low systemic absorption of the active component of the drug when applied externally makes an overdose almost impossible.
Side effect
Local reactions: eczema, photosensitization, contact dermatitis (itching, redness, swelling of the treated skin area, papules, vesicles, peeling).
Systemic reactions: generalized skin rash, allergic reactions (urticaria, angioedema, bronchospastic reactions), photosensitivity.
Drug interactions
Diclac can enhance the effect of drugs that cause photosensitization.
No clinically significant interaction with other drugs has been described.
Application during pregnancy and lactation
The drug is contraindicated in the third trimester of pregnancy.
The doctor determines the necessity of prescribing the drug in the first and second trimesters of pregnancy individually.
There is no experience of using the drug Diklak during lactation (breastfeeding).
special instructions
Diclak should only be applied to intact skin, avoiding contact with open wounds.
After application, do not apply an occlusive dressing.
Avoid contact of the drug on the eyes and mucous membranes.
Name ENG
DICLAC
Clinical and pharmacological group
NSAIDs for external use
ATX code
Diclofenac
Dosage
5% x 100g
Structure
100 g of the drug contains: active ingredient: diclofenac sodium?
5.0 g
excipients: isopropyl alcohol?
45.0 g
purified water ?
40.8 g
macrogol-7-glycerol cocoate - 6.0 g
hypromellose - 3.0 g
aromatic oil "Bouquet" WN 4507 - 0.2 g
Indications
Diseases of the musculoskeletal system: rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis, osteoarthritis of the peripheral joints and spine
rheumatic lesions of soft tissues.
Muscle pains of rheumatic and non-rheumatic origin.
Traumatic soft tissue injuries.
Contraindications
Hypersensitivity to diclofenac or other components of the drug, acetylsalicylic acid or other NSAIDs, "aspirin" asthma, pregnancy (III trimester), lactation, childhood (up to 6 years), violation of the integrity of the skin.
With care: hepatic porphyria (exacerbation), erosive and ulcerative lesions of the gastrointestinal tract, severe liver and kidney dysfunction, chronic heart failure, bronchial asthma, old age, pregnancy I and II trimester.
Storage conditions and periods
At a temperature not higher than 25 degrees.
Expiration date: 3 years
INN / Active ingredient
diclofenac sodium
Specifications
Category
Bruises, sprains
Scope of the drug
Musculoskeletal system
Release form
Gel
Manufacturer country
Germany
Package quantity, pcs
one
Minimum age from
6 years
Way of introduction
Outwardly
Vacation conditions
Without recipe
Brand name
Hexal
The amount of the dosage form in the primary package
100 g
Primary packaging type
Aluminum tube
Type of consumer packaging
Cardboard box
Pharmaco-therapeutic group
NSAIDs
Anatomical and therapeutic characteristics
M02AA15 Diclofenac
Dosage form
Gel for external use
Expiration date in days
1095
The target audience
Children
Dosage (volume) of the substance in the preparation
diclofenac sodium 5.0 g
Package weight, g
150
Mode of application
:
Outwardly.
For adults and children over 6 years of age, the drug is applied to the skin 2-3 times a day and rubbed lightly.
The required amount of the drug depends on the size of the painful area.
A single dose of the drug is up to 2 g (about 4 cm with a completely open tube mouth).
Wash your hands after applying the drug.
The duration of treatment depends on the indications and the observed effect.
After 2 weeks of using the drug, you should consult your doctor.
Drug action
:
Anti-inflammatory
,
Analgesic
,
Pain reliever
,
Decongestant
Information on technical characteristics, delivery set, country of manufacture "