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Characterization of patients with lupus nephritis included in a large cohort from the spanish society of rheumatology registry of patients with systemic lupus erythematosus (RELESSER)

[67] The Irish Medicines Board (IMB) issued a precautionary safety alert on February 27, 2009 regarding the use of "the unauthorised medicine Melanotan (I and II)", sold as a powder for injection, stating that "Melanotan is not yet authorised in Ireland and therefore the IMB cannot guarantee the efficacy, safety or quality of this product." [10] In its release, the IMB announced that its tests had found the presence of microbial contamination in a vial of water sold together with melanotan powder which "would expose recipients to a risk of serious infection"