This parameter therefore requires monitoring during the initiation, adjustment and withdrawal of treatment with dexketoprofen. Gastritis, constipation, dry mouth, flatulence Peptic ulcer, peptic ulcer haemorrhage or peptic ulcer perforation see section 4. Take the container with you, even if it is empty. What Keral is and what it is used for What you need to know before you take Keral How to take Keral Possible side effects How to store Keral Contents of the pack and other information 1. Contents of the pack and other information What Keral contains The active substance is dexketoprofen trometamol Patients with a history of gastrointestinal toxicity, particularly when elderly, should report any unusual abdominal symptoms especially gastrointestinal bleeding particularly in the initial stages of treatment.
In case of a relevant increase in such parameters, therapy must be discontinued. Distribution The distribution half-life and elimination half-life values of dexketoprofen are 0. Active ingredient dexketoprofen trometamol. What Keral is and what it is used for Keral is a pain killer from the group of medicines called non-steroidal anti-inflammatory drugs NSAIDs. In animals, administration of a prostaglandin synthesis inhibitor has been shown to result in increased pre- and post-implantation loss and embryo-foetal lethality. Further reading and references. Packaging Presentation 10 Or 20 Tablets. Gastrointestinal safety Gastrointestinal bleeding, ulceration or perforation which can be fatal, have been reported with all NSAIDs at anytime during treatment, with or without warning symptoms or a previous history of serious gastrointestinal events.
During treatment with non-steroidal anti-inflammatory drugs, fluid retention and swelling especially in the ankles and legsincreased blood pressure and heart failure have been tabldt. In case of combined prescription of dexketoprofen and a diuretic, it is essential to ensure that the patient is adequately hydrated and to monitor renal function at the start of the treatment see section 4. Brand Name 40 Enantyum Clinical studies performed on several pain models demonstrated effective mgg activity of dexketoprofen.
Do not keep out-of-date or unwanted medicines. Try taking the tablets after meals.
Reduced white blood cell count neutropeniafewer platelets in the blood thrombocytopenia. Latest Drug Information Updates. Warnings and precautions Talk to your doctor or pharmacist before taking Keral: Liver Safety Caution should be exercised in patients with impairment of hepatic functions. Therefore the safety and efficacy in children and adolescents have not been established and the product should not be used in children and adolescent.
Gastrointestinal safety Gastrointestinal bleeding, ulceration or perforation which can be fatal, have been mmg with all NSAIDs at anytime during treatment, with or without warning symptoms or a previous history of serious gastrointestinal events. Caution should be exercised in patients with impairment of renal functions. As it has been recognised for the whole pharmacological class of NSAIDs, dexketoprofen trometamol may cause changes of embryo-foetal survival in animal kegesse, both indirectly, through the gastrointestinal toxicity on the pregnant mothers, and directly upon the development of the foetus.
Distribution The distribution half-life and elimination half-life values of dexketoprofen are 0. Last tqblet on eMC: All non-selective NSAIDs can inhibit platelet aggregation and prolong bleeding time via inhibition of prostaglandin synthesis. Stop using Keral as soon as you notice the appearance of a skin rash, or any lesion inside the my or on the genitals, or any sign of an allergy. This information is intended for use by health professionals.
Elderly patients are more likely to be suffering from impaired hepatic function see section 4. Dosage Form Film Tablet. There are insufficient data to exclude such a risk for dexketoprofen. Dosage Strength Ketesse, Filmtabl 25 mg, ketesae Stk. Active ingredient dexketoprofen trometamol.
Anti-inflammatory painkillers like dexketoprofen are also called non-steroidal anti-inflammatory drugs NSAIDsor sometimes just ‘anti-inflammatories’. Alternatively, you can find an example of a manufacturer’s information leaflet filn the reference section below.
Fatigue, pain, asthenia, rigors, malaise.
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Clinical efficacy and safety Clinical studies performed on several pain models demonstrated effective analgesic activity of dexketoprofen. There is a theoretical risk that prostaglandin synthetase inhibitors may alter the efficacy of mifepristone.
The usual dose is either half a 25 mg tablet every hours, or one 25 mg tablet every eight hours. Dexketoprofen is used to treat short-term painful conditions such as muscular sprains and strainsperiod menstrual painand toothache.
Dexiren 25 Mg 20 Film Coated Tablets
What Keral looks like and contents of the pack Keral is supplied in packs containing 4, 10, 20, 30, 50 and film-coated tablets. Granules For Oral Solution. Keral tablets are contraindicated during third trimester of pregnancy and lactation see section 4. Increased surveillance in the presence of even mildly impaired renal function, as well as in the elderly.
Jeuveau Jeuveau prabotulinumtoxinA is a botulinum toxin type A formulation for the temporary improvement in the Keral should be discontinued at the first appearance of mb rash, mucosal lesions, or any other sign of hypersensitivity.
If dexketoprofen is used by a woman attempting to conceive, or during the first and second trimester of pregnancy, the dose should be kept as low and duration of treatment as ketese as possible. Brand Name Dexketoprofen Ratiopharm Brand Name 40 Aurovitas Dexketoprofen Patients appear to be at highest risk of these reactions early in the course of therapy, the onset of the reaction occurring in the majority of cases within the first month of treatment.
Similar medicinal products have produced gastrointestinal vomiting, anorexia, abdominal pain and neurological somnolence, vertigo, disorientation, headache disorders. Any ektesse medicinal product or waste material should be disposed of in accordance with local requirements.
Other information Particular caution tabley required in patients yablet The symptomatology following overdose is not known. Non-clinical data reveal no special hazard for humans based on conventional studies of safety pharmacology, genotoxicity and immunopharmacology. The other ingredients are maize starch, microcrystalline cellulose, sodium starch glycollate, glycerol palmitostearate, hypromellose, titanium dioxide, propylene glycol, macrogol Use in children and adolescents This medicine may not be used under age Serious skin reactions, some of them fatal, including exfoliative dermatitis, Stevens-Johnson syndrome, and toxic epidermal necrolysis, have been reported very rarely in association with the use of NSAIDs.
Increase clinical monitoring and check bleeding time more often.
By reporting side effects ktesse can help provide more information on the safety of this medicine. Symptomatic treatment of pain of mild to moderate intensity, such as musculo-skeletal pain, dysmenorrhoea, dental pain.
Keral – Summary of Product Characteristics (SmPC) – (eMC)
Did you find this information useful? Dosage Form Oral Solution Granulate. Exceptionally, varicella can be 255 the origin of serious cutaneous and soft tissues infectious complications.