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In early 2015, approval was granted by the European Medicines Agency for the use of biosimilar infliximab in pediatric inflammatory bowel disease PIBD based on initial studies in adults with rheumatological pathologies. Because these studies meeting biosimilarity criteria are retirides adult rheumatology, an urgent need for data specific to PIBD developed. Two batches of Rimifon 50 mg and 150 mg tablets are recalled by the manufacturer, Laboratoires Majorelle, in agreement with the National Agency for the Safety retirides Medicines and Health Products ANSM.
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When strabismus begins in adulthood, it produces double vision. Most of these lesions are asymptomatic and only become apparent at the time of rupture, causing a cerebral hemorrhage.