is kenacomb a steroid

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From part of the guide:. Bro, can i ask? Atlantica Indonesia now hv caps If someone is Lvthey should get a higher quality box, but that is all dependent on if the developers of AO Indonesia actually made that change.

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Is kenacomb a steroid


It does not contain all the available information.

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Testosterone propionat balkan pharmaceuticals anavar Do I need a prescription? Dosage Information Please consult your physician or pharmacist or refer to the product package. Intraarticular injection dosage for adults and adolescents for all indications. Other important Information onKenacomb Cream Missing a dose In case you miss a dose, use it as soon as you notice. Nystatin and gramicidin are not absorbed from intact skin or mucous membranes. Tell your doctor if your symptoms do not improve or they get worse. The information provided in Pharmacotherapeutic group of Kenacomb is based on data of another medicine with exactly the same composition as the Kenacomb.

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Undesirable effects may be minimised using the lowest effective dose for the minimum period. Frequent patient review is required to titrate the dose appropriately against disease activity see 4. Adrenal cortical atrophy develops during prolonged therapy and may persist for years after stopping treatment.

Withdrawal of corticosteroids after prolonged therapy must, therefore, always be gradual to avoid acute adrenal insufficiency and should be tapered off over weeks or months according to the dose and duration of treatment. During prolonged therapy any intercurrent illness, trauma or surgical procedure may require a temporary increase in dosage. If corticosteroids have been stopped following prolonged therapy they may need to be reintroduced temporarily.

Patients should carry steroid treatment cards, as appropriate, which give clear guidance on the precautions to be taken to minimise risk and which provide details of prescriber, drug, dosage and the duration of treatment. Patients should not be vaccinated or immunized with live vaccines while they are under treatment with moderate or high dose corticosteroids for longer than 2 weeks treatment, since a possible lack of an antibody response may predispose to medical, and particularly neurological, complications.

Intraarticular and periarticular corticosteroid use, or steroids given for less than 2 weeks, or in a long-term regular dosage of 10 mg daily are not considered a contraindication to use of live vaccines. If, during treatment, the patient develops serious reactions or acute infections, the treatment must be stopped and appropriate treatment given. Caution should be used in the event of exposure to chickenpox, measles or other communicable diseases, since the course of specific viral diseases such as chickenpox and measles may be particularly severe in patients treated with glucocorticoids.

At particular risk are immunocompromised immunosuppressed children and individuals with no history of chickenpox or measles infection. Menstrual irregularities may occur and in postmenopausal women vaginal bleeding has been observed. This possibility should be mentioned to female patients but should not deter appropriate investigations as indicated. Co-administration of Kenacomb hexacetonide with CYP3A4 inhibitors is not recommended unless the potential benefit of treatment outweighs the risk of systemic corticosteroid effects.

If the potential benefit of co-administration outweighs the increased risk of systemic corticosteroid side-effects, patients should be monitored for these effects. Visual disturbance may be reported with systemic and topical corticosteroid use. If a patient presents with symptoms such as blurred vision or other visual disturbances, the patient should be considered for referral to an ophthalmologist for evaluation of possible causes which may include cataract, glaucoma or rare diseases such as central serous chorioretinopathy CSCR which have been reported after use of systemic and topical corticosteroids.

It is recommended to monitor growth and development of children on prolonged corticosteroid therapy. It may provoke toxic and anaphylactoid reactions in children under 3 years of age. Benzyl alcohol has been linked to severe adverse reactions and death, especially in paediatric patients. Exposure to excessive quantities of benzyl alcohol has been linked to toxicity hypotension and metabolic acidosis , especially in neonates, and to an increased incidence of kernicterus, mainly in premature infants.

There have been rare cases of death, mainly in premature infants, linked to exposure to excessive quantities of benzyl alcohol. Premature and low-birth-weight infants, as well as patients taking high doses, are more likely to develop toxicity.

Patients with very rare hereditary problems of fructose intolerance should not take this medicine. If there is any reason to suppose that adrenal function is impaired, care must be taken while transferring patients from systemic steroid treatment to Kenacomb Allergy or Triamcinolone Nasal Spray. Patients taking steroids should consult their doctor before using this product.

In clinical studies with Kenacomb Allergy or Triamcinolone Nasal Spray administered intranasally, the development of localised infections of the nose and pharynx with Candida albicans has rarely occurred. When such an infection develops it may require treatment with appropriate local therapy and discontinuation of treatment with Kenacomb Allergy or Triamcinolone Nasal Spray.

Because of the inhibitory effect of corticosteroids on wound healing, patients who have had recent nasal surgery or recent prolonged nose-bleeds or any other nasal problems should consult their doctor before using this product. Systemic effects of nasal corticosteroids may occur, particularly at high doses prescribed for prolonged periods. These effects are much less likely to occur than with oral corticosteroids and may vary in individual patients and between different corticosteroid preparations.

Potential systemic effects may include Cushing's syndrome, Cushingoid features, adrenal suppression, growth retardation in children and adolescents, cataract, glaucoma and more rarely, a range of psychological or behavioural effects including psychomotor hyperactivity, sleep disorders, anxiety, depression or aggression particularly in children.

Treatment with higher than recommended doses may result in clinically significant adrenal suppression. If there is evidence of using higher than recommended doses then additional systemic corticosteroid cover should be considered during periods of stress or elective surgery. Kenacomb Allergy or Triamcinolone Nasal Spray has no known effect on the ability to drive and operate machines.

Adverse effects depend on the dose and the duration of treatment. Systemic adverse effects are rare, but may occur as a result of repeated periarticular injection. As with other intraarticular steroid treatments, transient adrenocortical suppression has been observed during the first week after injection.

This effect is enhanced if corticotropin or oral steroids are used concomitantly. Not known : menstrual irregularities, amenorrhoea and postmenopausal vaginal bleeding; hirsutism; development of a cushingoid state; secondary adrenocortical and pituitary unresponsiveness, particularly during periods of stress e. Not known : insomnia; exacerbation of existing psychiatric symptoms; depression sometimes severe ; euphoria; mood swings; psychotic symptoms.

Not known : increased intracranial pressure with papilloedema pseudotumor cerebri usually after treatment; headache. Not known : peptic ulcers with possibility of subsequent perforation and haemorrhage; pancreatitis. Not known : impaired wound healing; thin and fragile skin; petechiae and ecchymoses; facial erythema; increased sweating; purpurea; striae; acneiform eruptions; hives; rash. Not known : loss of muscle mass; osteoporosis; aseptic necrosis of the heads of the humerus and femur; spontaneous fractures; Charcot-like arthropathy.

Common: Local reactions include sterile abscesses, post-injection erythema, pain, swelling and necrosis at the injection site. Rare: Excess dosage or too-frequent administration of injections into the same site may cause local subcutaneous atrophy, which, due to the properties of the drug, will only return to normal after several months. Reporting suspected adverse reactions after authorisation of the medicinal product is important. Healthcare professionals are asked to report any suspected adverse reactions via the Yellow Card Scheme at: www.

The adverse events reported in clinical trials with Kenacomb Allergy or Triamcinolone Nasal Spray most commonly involved the mucous membranes of the nose and throat. Within each frequency grouping, undesirable effects are presented in order of decreasing seriousness. Systemic effects of nasal corticosteroids may occur, particularly when prescribed at high doses for prolonged periods. Healthcare professionals are asked to report any suspected adverse reactions via Yellow Card Scheme at: www.

Excess dosage or too-frequent administration of injections into the same site may cause local subcutaneous atrophy. If this occurs, recovery may take several months due to the long-term effect of the drug. Like any other nasally administered corticosteroid, acute overdosing with Kenacomb Allergy or Triamcinolone Nasal Spray is unlikely in view of the total amount of active ingredient present.

In the event that the entire contents of the bottle were administered all at once, via either oral or nasal application, clinically significant systemic adverse events would most likely not result. The patient may experience some gastrointestinal upset if taken orally. The mode of action of glucocorticoids is not fully known, but local injections are thought to have an anti-inflammatory effect.

The product is a microcrystalline water suspension with a depot effect. The anti-inflammatory potency of Kenacomb on a milligram by milligram comparison is approximately five times that of hydrocortisone. Triaminolone has practically no mineralocorticoid effect, so no sodium retention occurs. The efficacy and safety of Kenacomb hexacetonide in children and adolescents are based on the well-researched effects of glucocorticoids, which are the same in children and adults.

Published studies and current therapeutic guidelines for treatment of Juvenile Idiopathic Arthritis JIA indicate efficacy and safety in children and adolescents for the treatment of JIA. Triamcinolone acetonide is a more potent derivative of triamcinolone and is approximately 8 times more potent than prednisone. Although the precise mechanism of corticosteroid anti-allergic action is unknown, corticosteroids are very effective in the treatment of allergic diseases in man.

Kenacomb Allergy or Triamcinolone Nasal Spray does not have an immediate effect on allergic signs and symptoms. An improvement in some patient symptoms may be seen within the first day of treatment with Kenacomb Allergy or Triamcinolone Nasal Spray and relief may be expected in 3 to 4 days. When Kenacomb Allergy or Triamcinolone Nasal Spray is prematurely discontinued symptoms may not recur for several days. The hexacetonide ester is almost insoluble in water, so dissolution is slow and the effect in the tissue of the injection site lasts for a long time, from a few weeks to several months.

Single dose intranasal administration of micrograms of Kenacomb Allergy or Triamcinolone Nasal Spray in normal adult subjects and in adult patients with allergic rhinitis demonstrated minimal absorption of triamcinolone acetonide. The mean peak plasma concentration was approximately 0. The mean plasma drug concentration was less than 0.

The average terminal half life was 3. Dose proportionality was demonstrated in normal subjects and in patients following a single intranasal dose of micrograms or micrograms Kenacomb Allergy or Triamcinolone Nasal Spray. Following multiple doses in paediatric patients, plasma drug concentrations, AUC, C max and T max were similar to those values observed in adult patients.

Kenacomb hexacetonide is a potent teratogen in many animals. For example cleft palate has been reported in mice, rats, rabbits, and hamsters. CNS anomalies and cranial malformations have been observed in monkeys following gestational exposure. To date, however, no signs of teratogenicity of corticosteroids have been observed in humans. The environmental risk assessment has been performed according to European standards.

From these results it is assumed that the medicinal product is unlikely to represent a risk for the environment following the recommended use in patients. Like other corticosteroids, triamcinolone acetonide has been shown to be teratogenic in rats and rabbits. Teratogenic effects, including CNS and cranial malformations, have also been observed in non-human primates.

The use of solvents containing methylparaben, propylparaben, phenol, etc. The syringe should then be shaken gently, and the resulting solution used immediately thereafter. Kenacomb Print. Name of the medicinal product.

Special precautions for disposal and other handling. Components: Triamcinolone Acetonide. The information provided in Name of the medicinal product of Kenacomb is based on data of another medicine with exactly the same composition as the Kenacomb. Be careful and be sure to specify the information on the section Name of the medicinal product in the instructions to the drug Kenacomb directly from the package or from the pharmacist at the pharmacy.

Qualitative and quantitative composition. The information provided in Qualitative and quantitative composition of Kenacomb is based on data of another medicine with exactly the same composition as the Kenacomb. Be careful and be sure to specify the information on the section Qualitative and quantitative composition in the instructions to the drug Kenacomb directly from the package or from the pharmacist at the pharmacy. Therapeutic indications. The information provided in Therapeutic indications of Kenacomb is based on data of another medicine with exactly the same composition as the Kenacomb.

Be careful and be sure to specify the information on the section Therapeutic indications in the instructions to the drug Kenacomb directly from the package or from the pharmacist at the pharmacy. Pills; Substance-powder; Suspension for injection.

Nasal spray, suspension. The existing bacteria eventually die or are destroyed by the immune system. Gramicidin is a different type of antibiotic, and the combination of these two antibiotics provides treatment against a wide variety of bacteria that may infect the skin. Nystatin is an antifungal medicine. It kills fungi and yeasts by interfering with their cell membranes. Nystatin works by binding to a substance called ergosterol, which is a component of fungal cell membranes.

Binding to ergosterol disrupts the cell membrane and causes holes to appear. The cell membranes of fungi are vital for their survival. They keep unwanted substances from entering the cells and stop the contents of the cells from leaking out. As nystatin causes holes to appear in the cell membranes, essential constituents of the fungal cells can leak out. This kills the fungi. The combination of these anti-infective medicines with the anti-inflammatory triamcinolone is used to treat inflammatory skin conditions, such as eczema, that have become infected with bacteria, fungi or both.

Use with caution in Impaired hearing Leg ulcers Skin infections following extensive burns Not to be used in Acne vulgaris Children less than 1 year of age Chronic inflammatory disorder of the facial skin acne rosacea Inflammatory rash around the mouth perioral dermatitis Large areas of skin Skin infections with fungi not susceptible to nystatin Skin sores caused by tuberculosis The outer ear if you have a perforated ear drum Viral skin infections such as chickenpox or herpes simplex This medicine should not be used if you are allergic to one or any of its ingredients.

Pregnancy and breastfeeding Certain medicines should not be used during pregnancy or breastfeeding. However, other medicines may be safely used in pregnancy or breastfeeding providing the benefits to the mother outweigh the risks to the unborn baby. Always inform your doctor if you are pregnant or planning a pregnancy, before using any medicine.

The safety of this medicine in pregnancy has not been established. It should therefore be used with caution during pregnancy, and only if the benefits to the mother outweigh any risks to the foetus. There is no information available regarding the safety of this medicine during breastfeeding.

Seek medical advice from your doctor. Label warnings This medication is to be spread thinly and sparingly on the skin. Side effects Medicines and their possible side effects can affect individual people in different ways. Thinning of the skin Allergic reaction to active ingredient Stretch marks striae Groupings of fine blood vessels becoming prominent under the skin telangiectasia Increased hair growth hirsutism Impaired wound healing Small purplish blood spots in the skin ecchymoses Skin eruptions resembling acne The side effects listed above may not include all of the side effects reported by the drug's manufacturer.

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