No pharmacokinetic studies have been carried out in children.
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No information is present at this moment.
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No information is present at this moment.
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| Toxoplasmosis, congenital |
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| Toxoplasmosis, postnatal |
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Adjustment in renal impairment as specified:
In renal impairment, renal excretion of sulfadiazine and the N-acetyl metabolite decreases. This increases the risk of side effects.
No data are available on dose adjustment for dialysis.
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The complete list of all undesirable drug reactions can be found in the national Summary of Product Characteristics (SmPC) – click here
Nausea, vomiting, diarrhoea, dizziness, tinnitus, crystalluria, hypersensitivity reaction and abnormal blood counts.
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The complete list of all contra-indications can be found in the national Summary of Product Characteristics (SmPC) – click here
Serious abnormalities in the blood count, hypersensitivity to sulphonamides.
The complete list of all warnings and precautions can be found in the national Summary of Product Characteristics (SmPC) – click here
Caution is needed with exposure of the skin to sunlight or UV radiation due to the risk of photosensitivity. Stop the administration immediately if skin-related symptoms appear. It is recommended that an adequate fluid intake should be maintained or the urine made alkaline to prevent crystalluria.
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The complete list of all interactions can be found in the national Summary of Product Characteristics (SmPC) – click here
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| Trimethoprim and derivatives | ||
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| J01EA01 | ||
| Combinations of sulfonamides and trimethoprim, incl. derivatives | ||
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| J01EE01 | ||
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