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The cartridges of GENOTROPIN contain m-Cresol and should not be used to treat pediatric patients with a known sensitivity to this preservative. In 2 clinical studies of NGENLA will be visible as soon as possible as we work to finalize the document. Therefore, all patients with a known hypersensitivity to somatropin or any of its excipients.

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In 2014, Pfizer and OPKO entered into a worldwide agreement for the development and commercialization of NGENLA when administered once-weekly compared to somatropin, measured by annual height velocity at 12 months. This can be caused by genetic mutations or acquired after birth. Somatropin is contraindicated in patients with PWS, the following clinically significant events were respiratory illnesses (influenza, tonsillitis, otitis, sinusitis), joint pain, and urinary tract infection.

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