Special Warnings and Precautions for Use
Sulidor should not be applied to skin wounds or open lesions.
Avoid contact with eyes or mucous membranes; in case of accidental contact, wash immediately with water.
This medicine should never be ingested.
Hands should be washed after applying the gel. It should not be used with occlusive dressings.
Sulidor is not recommended for use in children under 12 years old.
Undesirable effects may be reduced by using the lowest effective dose for the shortest possible time.
Patients with gastrointestinal bleeding, active or suspected peptic ulcer, severe hepatic or renal dysfunction, severe coagulation disorders or with severe/uncontrolled cardiac insufficiency should be treated with caution.
Special caution should be used when treating patients with known hypersensitivity to other NSAIDs, since Sulidor has not been studied in individuals with hypersensitivity.
It cannot be excluded the possibility of these patients develop hypersensitivity during treatment. Since a burning sensation and, exceptionally, photodermatitis may occur with other topical NSAIDs, special attention should also be paid during treatment with Sulidor.
Patients should be cautioned against direct exposure to sunlight and sunbeds in order to reduce the risk of photosensitivity.
If symptoms persist or the condition worsens, consult your doctor.
To the extent that there is a possibility of dermal absorption of Sulidor, it is not possible to exclude the occurrence of systemic effects.
The risk of occurrence of these effects depends, among other factors, on the exposed surface, amount applied and period of exposure.
Skin safety of non-steroidal anti-inflammatory drugs (NSAIDs): Severe skin reactions associated with NSAID administration, some of which have been fatal – including exfoliative dermatitis, Stevens-Johnson syndrome and toxic epidermal necrolysis – have been reported rarely. It appears that the risk of occurrence of these reactions is higher at the beginning of the treatment; in most cases these reactions occur during the first month of treatment.
Treatment with Sulidor should be interrupted at the first signs of rash, mucosal lesions or other manifestations of hypersensitivity.
Sulidor contains methyl para-hydroxybenzoate (E218) and propyl para-hydroxybenzoate, which may cause allergic reactions (possibly delayed). Sulidor contains propylene glycol, which can cause skin irritation.
Fertility, pregnancy and breastfeeding: Sulidor should not be used during pregnancy or breastfeeding, unless clearly necessary, due to the lack of relevant data in these subpopulations.
Carefully read this information on the packaging and the package leaflet. In case of doubt or persistence of symptoms you should consult your doctor or pharmacist.
This website is exclusively for residents of Portugal.
Last Review: 24/07/2018