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• The composition of the injectable substances (all the elements they contain, of whatever nature).
• The benefits of the vaccine.
• The risks you have in detail of their nature, probability, magnitude and, if possible, time of occurrence.
• Clarify that the substance has only emergency authorization and not definitive, explaining in terms simple what difference do these two types of permissions make in specific order to private weighting of the above risks.
• That the adverse effects already detected be detailed, in their entirety by regularly updating this information.
• The controls to which the State is obliged by art. 2 inc. 5 of Law No. 9202 are carried out.